U.S. patent application number 17/210719 was filed with the patent office on 2022-03-17 for ocular implant containing a tyrosine kinase inhibitor.
The applicant listed for this patent is Ocular Therapeutix, Inc.. Invention is credited to Charles D. Blizzard, Arthur Driscoll, Rami El-Hayek, Michael Goldstein, Joseph Iacona, Peter Jarrett, Timothy S. Jarrett, Erica Kahn, Zachary Lattrell.
Application Number | 20220079876 17/210719 |
Document ID | / |
Family ID | |
Filed Date | 2022-03-17 |
United States Patent
Application |
20220079876 |
Kind Code |
A1 |
Blizzard; Charles D. ; et
al. |
March 17, 2022 |
OCULAR IMPLANT CONTAINING A TYROSINE KINASE INHIBITOR
Abstract
The invention relates to a sustained release biodegradable
ocular implant containing a tyrosine kinase inhibitor dispersed in
a hydrogel for the treatment of a retinal disease for an extended
period of time.
Inventors: |
Blizzard; Charles D.;
(Nashua, NH) ; Driscoll; Arthur; (Reading, MA)
; El-Hayek; Rami; (Norwood, MA) ; Goldstein;
Michael; (Cambridge, MA) ; Iacona; Joseph;
(Somerville, MA) ; Jarrett; Peter; (Burlington,
MA) ; Jarrett; Timothy S.; (Boston, MA) ;
Kahn; Erica; (Cambridge, MA) ; Lattrell; Zachary;
(Newburyport, MA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Ocular Therapeutix, Inc. |
Bedford |
MA |
US |
|
|
Appl. No.: |
17/210719 |
Filed: |
March 24, 2021 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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62994391 |
Mar 25, 2020 |
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63106276 |
Oct 27, 2020 |
|
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63148463 |
Feb 11, 2021 |
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International
Class: |
A61K 9/00 20060101
A61K009/00; A61K 31/4427 20060101 A61K031/4427; A61P 27/02 20060101
A61P027/02 |
Foreign Application Data
Date |
Code |
Application Number |
Apr 24, 2020 |
US |
PCT/US2020/029827 |
Claims
1. A method of treating an ocular disease in a patient in need
thereof, the method comprising administering to the patient a
sustained release biodegradable ocular implant comprising a
hydrogel and at least about 150 .mu.g of a tyrosine kinase
inhibitor (TKI), wherein TKI particles are dispersed within the
hydrogel.
2. The method of claim 1, wherein the tyrosine kinase inhibitor is
axitinib.
3. The method of claim 2, wherein the implant comprises axitinib in
an amount of about 150 .mu.g to about 1800 .mu.g.
4. The method of claim 2, wherein the implant comprises axitinib in
an amount of about 150 .mu.g to about 1200 .mu.g.
5. The method of claim 2, wherein the implant comprises axitinib in
an amount of about 480 .mu.g to about 750 .mu.g.
6. The method of claim 2, wherein the implant comprises axitinib in
an amount of about 160 pa to about 250 .mu.g.
7. The method of claim 1, wherein the implant is administered once
during a treatment period of at least 3 months.
8. The method of claim 7, wherein the treatment period is about 6
to about 9 months.
9. The method of claim 7, wherein the TKI is axitinib and an
axitinib dose per eye administered once during the treatment period
is from about 150 .mu.g to about 1800 .mu.g, wherein the dose is
contained in one implant or in two or more implants administered
concurrently.
10. The method of claim 9, wherein the axitinib dose per eye
administered once during the treatment period is from about 150
.mu.g to 1200 .mu.g.
11. The method of claim 1, wherein the ocular disease is a retinal
disease.
12. The method of claim 11, wherein the retinal disease is selected
from the group consisting of neovascular age-related macular
degeneration (AMD), diabetic macular edema (DME), retinal vein
occlusion (RVO) or a combination thereof.
13. The method of claim 12, wherein the retinal disease is AMD.
14. The method of claim 13, wherein the treatment is effective in
reducing, essentially maintaining or preventing a clinically
significant increase of the central subfield thickness as measured
by optical coherence tomography in a patient whose central subfield
thickness is elevated.
15. The method of claim 14, wherein the patient has been diagnosed
with primary subfoveal neovascularization and has or has not been
previously treated with an anti-VEGF agent.
16. The method of claim 1, wherein the implant is administered by
injection into the vitreous humor.
17. The method of claim 16, wherein the implant is injected by
means of a needle for injection.
18. The method of claim 17, wherein the needle for injection is a
needle that has a gauge size of 22 to 30.
19. The method according to claim 1, wherein concurrently or in
combination with the treatment with the sustained release ocular
implant an anti-VEGF agent is administered to the patient.
20. The method of claim 19, wherein an anti-VEGF agent is
administered in combination with the implant, and is administered
within about 1, about 2 or about 3 months from the administration
of the implant.
21. The method of claim 19, wherein the anti-VEGF agent is selected
from the group consisting of aflibercept, bevacizumab, pegaptanib,
ranibizumab, and brolucizumab and is administered by intravitreous
injection.
22. The method of claim 1, wherein the implant is administered by
injection into the vitreous humor and the TKI is axitinib, wherein
a dose administered per eye once during a treatment period of at
least 3 months is from about 150 .mu.g to about 1800 .mu.g and is
contained in one or more implant(s) administered concurrently.
23. The method of claim 1, wherein the implant is administered by
injection into the vitreous humor and the TKI is axitinib, wherein
a dose administered per eye once during a treatment period of at
least 3 months is from about 480 .mu.g to about 750 .mu.g axitinib
and is contained in one implant.
24. The method of claim 1, wherein the hydrogel comprises
polyethylene glycol (PEG) units.
25. The method of claim 24, wherein the hydrogel comprises PEG
units that have a number average molecular weight of about 20,000
Daltons.
26. The method of claim 24, wherein the PEG units comprise 4-arm
and/or 8-arm PEG units.
27. The method of claim 24, wherein the hydrogel comprises
crosslinked PEG units and the crosslinks between the PEG units
include a group represented by the following formula ##STR00008##
wherein m is an integer from 0 to 10.
28. The method of claim 27, wherein m is 6.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] The present invention claims priority to U.S. Provisional
Application Ser. No. 62/994,391 filed Mar. 25, 2020, to
International Application PCT/US2020/029827 filed 24 Apr. 2020, to
U.S. Provisional Application Ser. No. 63/106,276 filed Oct. 27,
2020, and to U.S. Provisional Application Ser. No. 63/148,463 filed
Feb. 11, 2021, which are all hereby incorporated by reference
herein.
TECHNICAL FIELD
[0002] The present invention relates to the treatment of ocular
diseases, for example neovascular age-related macular degeneration
(AMD), also referred to as "wet AMD". According to the present
invention, ocular diseases are treated by administering an
injection (e.g., intravitreally) of an implant that is
biodegradable and provides sustained release of a tyrosine kinase
inhibitor such as axitinib.
BACKGROUND
[0003] Macular diseases, including AMD, are among the leading
causes of visual impairment and irreversible blindness in the world
for people over the age of 50. Specifically, AMD was one of the
most common retinal diseases in the United States (US) in 2019,
affecting approximately 16.9 million people, and this is expected
to grow to 18.8 million people in 2024 (Market Scope. Ophthalmic
Comprehensive Reports. 2019 Retinal Pharmaceuticals Market Report:
A Global Analysis for 2018 to 2019, September 2019). AMD can be
subdivided into different disease stages. Early AMD is
characterized by the presence of a few (<20) medium-size drusen
or retinal pigmentary abnormalities. Intermediate AMD is
characterized by at least one large druse, numerous medium-size
drusen, or geographic atrophy that does not extend to the center of
the macula. Advanced or late AMD can be either non-neovascular
(dry, atrophic, or non-exudative) or neovascular (wet or
exudative). Advanced non-neovascular AMD is characterized by drusen
and geographic atrophy extending to the center of the macula.
Advanced neovascular AMD is characterized by choroidal
neovascularization and its sequelae (Jager et al., Age-related
macular degeneration. N Engl J Med. 2008; 358(24):2606-17).
[0004] The more advanced form of wet AMD is characterized by an
increase in vascular endothelial growth factor (VEGF), which
promotes the growth of new vessels (angiogenesis) that grow beneath
the retina and leak blood and fluid into and below the macular and
subretinal space. Successful interference of this pathway has been
achieved with the development of inhibitors of vascular endothelial
growth factor subtypes, i.e., VEGF inhibitors, initially used to
treat various cancers. Photodynamic therapy in combination with
anti-VEGF and steroid administration are currently reserved as a
second-line therapy for patients not responding to monotherapy with
an anti-VEGF agent (Al-Zamil et al., Recent developments in
age-related macular degeneration: a review. Clin Intery Aging.
2017; 12:1313-30).
[0005] Other common retinal diseases are diabetic macular edema
(DME) and retinal vein occlusion (RVO). DME was one of the most
common retinal diseases in the US in 2019, affecting approximately
8 million people, and this is expected to grow to 8.8 million
people in 2024 (Market Scope 2019, supra). The condition is
categorized by a decrease in retinal tension and an increase in
vascular pressure caused by the upregulation of VEGF, retinal
vascular autoregulation (Browning et al., Diabetic macular edema:
evidence-based management. 2018 Indian journal of ophthalmology,
66(1), p. 1736) and inflammatory cytokines and chemokines (Miller
et al., Diabetic macular edema: current understanding,
pharmacologic treatment options, and developing therapies. 2018,
Asia-Pacific Journal of Ophthalmology, 7(1):28-35). The changes
that occur from these inflammatory and vasogenic mediators result
in the breakdown of the blood retinal barrier (BRB) in the vascular
endothelium (Miller et al, supra). Hard exudates enter into the
extracellular space causing blurred and distorted central vision,
resulting in a decrease in the patient's visual acuity
(Schmidt-Erfurth et al., guidelines for the Management of Diabetic
Macular Edema by the European Society of Retina Specialists
(EURETINA). 2017, Ophthalmologica. 237(4): 185-222). On average, a
patient will experience an 8% decrease in visual acuity after 3
years following the start of the condition.
[0006] The basis of all available treatments for DME is to try to
control the metabolic functions of hyperglycemia and blood pressure
(Browning et al., supra). Anti-VEGF therapy is currently considered
a first line therapy in the standard of care treatment of DME as it
is proven to be less destructive and damaging than other treatment
methods (Schmidt-Erfurth et al., supra). The pharmacological route
is beneficial because the drugs are manufactured to specifically
target VEGF pathways and inhibit the upregulation that occurs with
DME (Miller et al., supra). Other treatment options include
intravitreal corticosteroid injections, focal laser
photocoagulation, and vitrectomy (Browning et al., supra).
[0007] RVO affected approximately 1.3 million people in the US in
2019 and is predicted to affect 1.4 million people in the US in
2024 (Market Scope 2019, supra). RVO is a chronic condition in
which the retinal circulation contains a blockage leading to
leakage, retinal thickening, and visual impairment (Ip and
Hendrick, Retinal Vein Occlusion Review. 2018, Asia-Pacific Journal
of Ophthalmology, 7(1):40-45; Pierru et al., Occlusions veineuses
retiniennes retinal vein occlusions. 2017, Journal Francais
d'Ophtalmologie, 40(8):696-705). The condition is typically seen in
patients 55 and older who have a pre-existing condition such as
high blood pressure, diabetes, and glaucoma. RVO does not have a
projected course as it can either deteriorate a patient's vision
quickly or remain asymptomatic. Prognosis of RVO and associated
treatment options depend on the classification of the disease as
the different variants have different risk factors despite behaving
similarly. Classification of the disease is categorized depending
on the location of the impaired retinal circulation: branch retinal
vein occlusion (BRVO), hemiretinal vein occlusion (HRVO), and
central retinal vein occlusion (CRVO). BRVO is more common
affecting 0.4% worldwide and CRVO affecting 0.08% worldwide.
Studies show that BRVO is more prevalent in Asian and Hispanic
groups compared to Caucasians (Ip and Hendrick, supra).
[0008] Treatment of RVO currently includes symptomatic maintenance
of the condition to avoid further complications, macular edema, and
neovascular glaucoma. Anti-VEGF treatment is currently the standard
of care treatment and may temporarily improve vision. Other
treatment options include lasers, steroids, and surgery (Pierru et
al., supra).
[0009] Anti-VEGF agents are currently considered the standard of
care treatment for wet AMD, DME, and RVO. The first treatment
approved for wet AMD by the FDA in 2004 was MACUGEN.RTM.
(pegaptanib sodium injection by Bausch & Lomb). Since then,
LUCENTIS.RTM. (ranibizumab injection by Genentech, Inc.) and
EYLEA.RTM. (aflibercept injection by Regeneron Pharmaceuticals,
Inc.) have been approved for the treatment of wet AMD in 2006, and
2011 respectively, as well as DME and macular edema following RVO.
Additionally, in October 2019, BEOVU.RTM. (brolucizumab injection
by Novartis Pharmaceuticals Corp) was approved by the FDA for the
treatment of wet AMD. Other developments are reported in Amadio et
al., Targeting VEGF in eye neovascularization: What's new?: A
comprehensive review on current therapies and oligonucleotide-based
interventions under development. 2016, Pharmacological Research,
103:253-69.
[0010] However, despite these advancements, there are limitations
to anti-VEGF treatment. Most patients currently require multiple
injections (such as monthly) essentially for the rest of their
lives due to rapid vitreous clearance. Moreover, not all patients
respond to anti-VEGF treatment. Additionally, these treatment
options further have potential risks associated with administration
including infection, macular atrophy, loss of vision over time,
retinal detachment and elevated intraocular pressure (IOP). Patient
complaints include discomfort, eye pain, decreased vision, and
increased photosensitivity. In addition to the burden on the
patient and risks associated with frequent injections, there are
other limitations that are known to be associated with current
anti-VEGF treatments such as the potential risk of immunogenicity,
complex manufacturing requirement of biologics, macular atrophy,
and retinal vasculitis. Importantly, regardless of the number of
medications, patients are currently expected to remain on treatment
indefinitely.
[0011] Tyrosine kinase inhibitors were developed as
chemotherapeutics that inhibit signaling of receptor tyrosine
kinases (RTKs), which are a family of tyrosine protein kinases.
RTKs span the cell membrane with an intracellular (internal) and
extracellular (external) portion. Upon ligand binding to the
extracellular portion, receptor tyrosine kinases dimerize and
initiate an intracellular signaling cascade driven by
autophosphorylation using the coenzyme messenger adenosine
triphosphate (ATP). Many of the RTK ligands are growth factors such
as VEGF. VEGF relates to a family of proteins binding to
VEGF-receptor (VEGFR) types, i.e. VEGFR1-3 (all RTKs), thereby
inducing angiogenesis. VEGF-A, which binds to VEGFR2, is the target
of the anti-VEGF drugs described above. Besides VEGFR1-3 several
other RTKs are known to induce angiogenesis such as
platelet-derived growth factor receptor (PDGFR) activated by PDGF
or stem cell growth factor receptor/type III receptor tyrosine
kinase (c-Kit) activated by stem cell factor.
[0012] Some TKIs have been evaluated for the treatment of AMD via
different administration routes, including pazopanib
(GlaxoSmithKline: NCT00463320), regorafenib (Bayer: NCT02348359),
and PAN90806 (PanOptica: NCT02022540) all administered as eye
drops, as well as X-82, an oral TKI (Tyrogenex; NCT01674569,
NCT02348359). However, topically applied eye drops result in poor
penetration into the vitreous and limited distribution to the
retina due to low solution concentration of TKIs, which tend to
have low water solubility, and short residence time of the TKIs on
the ocular surface. Moreover, drug concentration upon topical
administration is difficult to control due to wash out or user
error. Furthermore, systemic administration of TKIs is not
practicable, as high doses are required to achieve effective
concentrations of the drug in the eye and particularly at the
desired tissue. This leads to unacceptable side effects due to high
systemic exposure. In addition, drug concentrations are difficult
to control. Alternatively, intravitreal injections of TKI
suspensions have been performed. However, this way of
administration results in rapid clearance of the drug and therefore
injections have to be repeated frequently, such as on a daily or at
least a monthly basis. In addition, several TKIs are poorly soluble
which leads to the formation of aggregates upon intravitreal
injection, which can migrate or settle onto the retina and lead to
local contact toxicity and holes, such as macular or retinal
holes.
[0013] Thus, there is an urgent need for an improved treatment of
ocular diseases such as AMD, DME, and RVO with TKIs, which is
effective over an extended period of time avoiding the need for
frequent (monthly or even daily) injections which are currently
required for common anti-VEGF therapies, especially for individuals
not responding to anti-VEGF therapies (e.g. up to 33% of subjects
with DME).
[0014] All references disclosed herein are hereby incorporated by
reference in their entireties for all purposes.
OBJECTS AND SUMMARY OF THE INVENTION
[0015] It is an object of certain embodiments of the present
invention to provide an ocular implant comprising a tyrosine kinase
inhibitor (TKI) such as axitinib that is effective for treating
ocular diseases such as neovascular age-related macular
degeneration (AMD), DME, and RVO in a patient for an extended
period of time.
[0016] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a tyrosine
kinase inhibitor (TKI) such as axitinib that provides for sustained
release of the TKI into the eye.
[0017] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that is pre-loaded into a syringe, thereby avoiding
contamination of the implant prior to injection as no further
preparation steps are needed.
[0018] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that is sufficiently biodegradable, i.e., cleared from the
eye within a time coinciding with TKI release, avoiding floaters
within the patient's eye (empty implant vehicle residues) and/or
avoiding the need for removal of the empty implant from the eye
after the treatment period.
[0019] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that is biodegradable, wherein decomposition of the
implant into smaller particles that may e.g. impact vision are
avoided during implant degradation.
[0020] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib, wherein the stability of the ocular implant is less
affected by varying environments in the eye such as vitreous humor
viscosity, pH of the vitreous humor, composition of the vitreous
humor and/or intraocular pressure (IOP) when compared to hydrogels
formed in situ after injection.
[0021] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that is biocompatible and non-immunogenic due to the
implant being free or substantially free of animal- or
human-derived components.
[0022] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that is free of preservatives, such as antimicrobial
preservatives.
[0023] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that is easy to inject, in particular intravitreally.
[0024] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that contains a therapeutically effective amount of said
TKI but is relatively small in length and/or diameter.
[0025] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that is dimensionally stable when in a dry state but
changes its dimensions upon hydration, e.g. after administration to
the eye.
[0026] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that has a small diameter when in a dry state to fit into
the lumen of a fine-diameter needle (such as a 22- to 30-gauge
needle) and increases in diameter but decreases in length upon
hydration, e.g. after administration to the eye; thus, providing a
minimally invasive method of administration.
[0027] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that is injected in a dry form and hydrates in situ (i.e.
in the eye) when injected.
[0028] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that when placed in the eye has low TKI concentration at
the implant surface thereby avoiding toxicity of the TKI when the
implant gets in contact with ocular cells or tissues such as the
retina.
[0029] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that is stable and has a defined shape and surface area
both in a dry state prior to as well as in a hydrated state after
the injection (i.e. inside the eye).
[0030] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that is easy to handle, in particular that does not spill
or fragment easily.
[0031] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that enables administration of an exact dose (within a
broad dose range), thereby avoiding the risk of over- and
under-dosing.
[0032] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that generally stays in the area of the eye to which it
was administered.
[0033] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib, wherein the implant causes minimal or no visual
impairment after administration.
[0034] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that is safe and well tolerated.
[0035] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that does not induce severe adverse events, such as severe
ocular adverse events.
[0036] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that provides for sustained release of a therapeutically
effective amount of the TKI such as axitinib over an extended
period of time, such as over a period of up to 3 months or longer,
such as at least 6, at least 9, at least 11 months, or at least 13
months.
[0037] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that provides for sustained release of a TKI such as
axitinib over an extended period of time, such as over a period of
up to 3 months or longer, such as at least 6, at least 9, at least
11 months, or at least 13 months, thereby avoiding the need for
frequent implant administrations.
[0038] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that provides for sustained release of the TKI such as
axitinib over an extended period of time, such as over a period of
up to 3 months or longer, such as at least 6, at least 9, at least
11 months, or at least 13 months, thereby inhibiting angiogenesis
over this period of time.
[0039] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that provides for sustained release of the TKI over an
extended period of time, such as over a period of up to 3 months or
longer, such as at least 6, at least 9, at least 11 months, or at
least 13 months, wherein the TKI levels in ocular tissues such as
the retina and the choroid, as well as the vitreous humor are
consistently maintained at a therapeutically efficient level, in
particular at a level sufficient for inhibition of angiogenesis,
over this period of time.
[0040] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that provides for sustained release of a TKI such as
axitinib over an extended period of time, such as over a period of
up to 3 months or longer, such as at least 6, at least 9, at least
11 months, or at least 13 months, wherein no toxic concentrations
of the TKI are observed in ocular tissues such as the retina and
the choroid, as well as the vitreous humor over this period of
time.
[0041] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that provides for sustained release of a TKI such as
axitinib over an extended period of time, such as over a period of
up to 3 months or longer, such as at least 6, at least 9, at least
11 months, or at least 13 months, wherein the TKI is not
accumulating in the anterior chamber of the eye.
[0042] Another object of certain embodiments of the present
invention is to provide an ocular implant comprising a TKI such as
axitinib that provides sustained release of a TKI over an extended
period of time, such as over a period of up to 3 months or longer,
such as at least 6, at least 9, at least 11 months, or at least 13
months, wherein the TKI is not or is not substantially resorbed
systemically thereby substantially avoiding systemic toxicity.
[0043] Another object of certain embodiments of the present
invention is to provide a method of treating ocular diseases such
as AMD, DME, and RVO in a patient in need thereof, for a treatment
period of up to 3 months or longer, such as at least 6, at least 9,
at least 11 months, or at least 13 months.
[0044] Another object of certain embodiments of the present
invention is to provide a method of treating ocular diseases such
as AMD, DME, and RVO in a patient in need thereof, for a treatment
period of up to 3 months or longer, such as at least 6, at least 9,
at least 11 months, or at least 13 months, without the need for the
administration of rescue medication during the treatment period, or
wherein rescue medication is required to be administered only
rarely, such as 1, 2 or 3 times, during the treatment period.
[0045] Another object of certain embodiments of the present
invention is to provide a method of treating ocular diseases such
as AMD, DME, and RVO in a patient in need thereof, such as a
patient who has been treated with anti-VEGF before or a patient who
is naive for anti-VEGF treatment.
[0046] Another object of certain embodiments of the present
invention is to provide a method of treating ocular diseases such
as AMD, DME, and RVO in a patient in need thereof, such as a
patient who has been treated with anti-VEGF before and has not
responded to the previous anti-VEGF treatment.
[0047] Another object of certain embodiments of the present
invention is to provide a method of treating ocular diseases such
as AMD, DME, and RVO in a patient in need thereof, such as a
patient with a diagnosis of primary subfoveal neovascularization
(SFNV) secondary to AMD.
[0048] Another object of certain embodiments of the present
invention is to provide a method of treating ocular diseases such
as AMD, DME, and RVO in a patient in need thereof, such as a
patient with a diagnosis of previously treated subfoveal
neovascularization (SFNV) secondary to neovascular AMD with leakage
involving the fovea, who has been previously treated with
anti-VEGF.
[0049] Another object of certain embodiments of the present
invention is to provide a method of manufacturing an ocular implant
comprising a TKI such as axitinib.
[0050] Another object of certain embodiments of the present
invention is to provide a method of protecting an ocular implant
from premature hydration during storage and handling, wherein the
ocular implant is sensitive to moisture such that it for instance
changes its dimensions upon hydration.
[0051] Another object of certain embodiments of the present
invention is to provide a method of minimizing potential tissue
damage during injection of an ocular implant.
[0052] Another object of certain embodiments of the present
invention is to provide a kit comprising one or more ocular
implants comprising a TKI such as axitinib and optionally
comprising a means for injecting the ocular implant.
[0053] Another object of certain embodiments of the present
invention is to provide a method of reducing the central subfield
thickness as measured by optical coherence tomography in a patient
whose central subfield thickness is elevated due to an ocular
disease involving angiogenesis by for instance reducing retinal
fluid.
[0054] Another object of the present invention is to provide a
method of essentially maintaining or preventing a clinically
significant increase of the central subfield thickness as measured
by optical coherence tomography in a patient whose central subfield
thickness is elevated due to an ocular disease involving
angiogenesis while not increasing retinal fluid.
[0055] Another object of certain embodiments of the present
invention is to provide a method of reducing, essentially
maintaining or preventing a clinically significant increase of the
central subfield thickness as measured by optical coherence
tomography in a patient whose central subfield thickness is
elevated due to an ocular disease involving angiogenesis while
improving or at least not impairing the patient's visual acuity as
measured for instance by means of best corrected visual acuity.
[0056] Another object of certain embodiments of the present
invention is to provide a method of improving the vision of a
patient whose vision is impaired due to an ocular disease involving
angiogenesis.
[0057] Another object of certain embodiments the present invention
is to provide a method of improving the vision of a patient whose
vision is impaired due to the presence of retinal fluid (caused for
instance by an ocular disease involving angiogenesis) by means of
reducing retinal fluid in the patient (as for instance evidenced by
a reduction the central subfield thickness as measured by optical
coherence tomography).
[0058] One or more of these objects of the present invention and
others are solved by one or more embodiments as disclosed and
claimed herein.
[0059] The individual aspects of the present invention are
disclosed in the specification and claimed in the independent
claims, while the dependent claims claim particular embodiments and
variations of these aspects of the invention. Details of the
various aspects of the present invention are provided in the
detailed description below.
[0060] Throughout this application various references are cited.
The disclosures of these references are hereby incorporated by
reference into the present disclosure. In case of conflict, the
disclosure in the present application prevails.
BRIEF DESCRIPTION OF THE DRAWINGS
[0061] FIG. 1 Schematic representation of one embodiment of the
implant packaging. In this embodiment, implants are pre-loaded into
thin-walled needles separately packaged from the injection device.
An all-in-one device with needles already connected to the
injection device is also possible.
[0062] FIG. 2 Schematic representation of one embodiment of implant
localization. After injection the implant hydrates in situ while
maintaining a cylindrical shape. The implant is localized in the
posterior part of the eye.
[0063] FIG. 3 Schematic representation of hydrogel biodegradation
over time. As the drug is released, a clearance zone is formed
(black) as low solubility drug particles (white) gradually dissolve
and drug diffuses from hydrogel to the aqueous surrounding (as for
instance the vitreous humor). Over time, the gel degrades and is
resorbed, while drug diffuses out. During the degradation process,
the gel gradually swells until degradation is advanced to the point
of shrinkage and distortion.
[0064] FIG. 4A and FIG. 4B One embodiment of in vitro axitinib
release per day for different implants. FIG. 4A shows in vitro
axitinib release under non-sink dissolution conditions from
different implants, comprising an axitinib dose of 625, 716, 245,
and 490 (2.times.245) .mu.g. FIG. 4B shows in vitro accelerated
axitinib release from a 556 .mu.g implant.
[0065] FIG. 5A and FIG. 5B One embodiment of low dose study in
rabbits. FIG. 5A shows infrared reflectance (IR) of 1, 2, and 3
implants in rabbits one month post injection. The overall shape of
the implants remained intact independent of the number of implants
administered. FIG. 5B shows vascular leakage was efficiently
suppressed for all three doses (15, 30, and 45 .mu.g) after 1
month, while vascular leakage was high for the control animals
without implant. Error bars represent standard deviation (SD;
solely upper error bars presented).
[0066] FIG. 6 One embodiment of infrared reflectance (IR) and
optical coherence tomography (OCT) imaging of rabbit eyes. IR/OCT
images of retinal morphology after 1, 3, and 6 months after implant
injection, respectively. Retinal morphology was normal.
[0067] FIG. 7A and FIG. 7B One embodiment of biodegradation of
implant and inflammation. FIG. 7A shows significant biodegradation
of the hydrogel component of the implant in rabbit eye was observed
over time. At weeks 4 and 8 after injection the implant was still
intact, whereas at week 12 early stages of hydrogel degradation
were visible. Implant was further narrowed at week 16 due to loss
of hydrogel structure. Finally, hydrogel was absent after 20 and 26
weeks and free (undissolved) axitinib particles (white specs) were
visible in proximity to the former implant site. FIG. 7B shows
histopathological analysis demonstrated no inflammation after 26
weeks in regions of un-dissolved axitinib. Images are presented at
20.times. magnification (scale: 1000 .mu.m) and 200.times.
magnification (scale: 100 .mu.m).
[0068] FIG. 8 One embodiment of suppression of vascular leakage in
rabbits challenged with VEGF following administration of an
axitinib implant with a dose of 227 .mu.g. Vascular leakage scores
(0 (normal) to 4 (severe leakage)) are presented in dependency of
the time (months) after VEGF challenge for animals with and without
the implant. Effective suppression of vascular leakage was observed
for animals having the implant for a duration of 6 months. Error
bars represent standard deviation (SD; solely upper error bars
presented).
[0069] FIG. 9 One embodiment of infrared reflectance (IR) imaging
of two implants in rabbit eyes. Implants show degradation over
time. Implants were intact at days 27 to 117, while implant
narrowing was observed due to hydrogel degradation observed on days
141 and 195. Remaining axitinib particles merged into a single
monolithic structure on days 141 and 195. Free axitinib particles
(white specs) were noted in proximity to the former implant site
post hydrogel degradation.
[0070] FIG. 10 One embodiment of infrared reflectance (IR) imaging
of two implants in rabbit eyes. The implant was intact during 0.5
to 3 months after injection. After 6 months, the implant narrowed
due to hydrogel degradation and remaining axitinib particles merged
into a single monolithic structure. Free axitinib particles (white
specs) were noted in proximity to the former implant site post
hydrogel degradation at 24 months up to 38 months.
[0071] FIG. 11 One embodiment of suppression of vascular leakage in
rabbits challenged with VEGF following administration of two
axitinib implants with a total dose of 290 .mu.g without (group 1)
and with (group 2) co-administration of Avastin.RTM.. Vascular
leakage scores (0 (normal) to 4 (severe leakage)) are presented in
dependency of the time (months) after VEGF challenge for animals
from group 1 and 2 and for animals without an implant. Significant
suppression of vascular leakage was observed for all groups of
animals having the implants. Error bars represent standard
deviation.
[0072] FIG. 12 One embodiment of fluorescein angiography (FA)
images revealed significant leakage, with fluorescein seen actively
leaking from vasculature immediately following injection of
fluorescein 48 hours after the VEGF challenge in the control
animals (upper panel) and complete inhibition of leakage from
vessels of rabbit eyes comprising the implants (lower panel).
Images were collected after VEGF challenge 1 month after the
implant injection.
[0073] FIG. 13 One embodiment of average vascular leakage score for
rabbits which were not treated with implant or anti-VEGF
therapeutic (white squares and dashed line), rabbits which were
treated with Avastin.RTM. only (black triangles, curve fit until 3
months), rabbits with implants (black squares, solid line until 12
months), and rabbits with implants and Avastin.RTM. (striped
squares and dashed line until 12 months). Vascular leakage was
efficiently inhibited for 12 months for all animals that received
the implants. Animals solely treated with anti-VEGF therapeutic
showed rapid onset of leakage inhibition in the first 2 to 4 weeks,
but leakage re-occurred after 3 months. Values represent mean and
standard error of the mean (SEM).
[0074] FIG. 14A and FIG. 14B One embodiment of in vitro axitinib
release from a 200 .mu.g implant. FIG. 14A shows axitinib was
completely released from the 200 .mu.g implant after 225 days as
observed by the in vitro real-time assay. FIG. 14B shows axitinib
was completely released from the 200 .mu.g implant after 12 days as
observed by the in vitro accelerated assay. In vitro data were not
indicated for in vivo release observed.
[0075] FIG. 15 One embodiment of IR images of subject #1 from
cohort 2 (2 implants, 400 .mu.g axitinib in total per eye).
Implants are clearly visible and well-shaped on the injection day.
After 9 months, implants are fully degraded while undissolved
axitinib is remaining at the former implant locations. The
undissolved axitinib continues to release drug, while after 11
months almost no undissolved axitinib is left.
[0076] FIG. 16 One embodiment of spectral domain optical coherence
tomography (SD-OCT) images from the study eye of subject #1 of
cohort 1 (1 implant, 200 .mu.g axitinib in total per eye). For this
treatment naive subject a significant reduction in central subfield
thickness (CSFT) was observed while best corrected visual acuity
(BCVA) was not impaired over 10.5 months.
[0077] FIG. 17 One embodiment of central subfield thickness (CSFT)
in the study eyes of patients suffering from neovascular
age-related macular degeneration (wet AMD) treated with axitinib
implants (one implant, total dose of 200 .mu.g: cohort 1; two
implants, total dose of 400 .mu.g: cohort 2; three implants, total
dose of 600 .mu.g: cohort 3a; two implants, total dose of 400 .mu.g
and concurrent initial anti-VEGF: cohort 3b). Presented in this
chart are mean changes in CSFT with standard error of the mean
(SEM) compared to the baseline value. For this chart: Six patients
were followed in cohort 1 until month 9. Seven patients were
followed in cohort 2 until month 12, five until month 14 and two
until month 16. Six patients were followed in cohort 3a until day
14, five until month 2, two until month 4.5, and one until months 6
and 7.5. Two patients were followed in cohort 3b until month 3, and
one until month 4.5. Follow-up is ongoing.
[0078] FIG. 18 One embodiment of best corrected visual acuity
(BCVA) in the study eyes of patients suffering from neovascular
age-related macular degeneration (wet AMD) treated with axitinib
implants (one implant, total dose of 200 .mu.g: cohort 1; two
implants, total dose of 400 .mu.g: cohort 2; three implants, total
dose of 600 .mu.g: cohort 3a; two implants, total dose of 400 .mu.g
and concurrent initial anti-VEGF: cohort 3b). Presented in this
chart are mean changes in BCVA with standard error of the mean
(SEM) compared to the baseline value in Early Treatment Diabetic
Retinopathy Study (ETDRS) Letter Score (a representative value for
letters that can be read correctly at a certain distance). For this
chart (as for FIG. 17 above): Six patients were followed in cohort
1 until month 9. Seven patients were followed in cohort 2 until
month 12, five until month 14 and two until month 16. Six patients
were followed in cohort 3a until day 14, five until month 2, two
until month 4.5, and one until months 6 and 7.5. Two patients were
followed in cohort 3b until month 3, and one until month 4.5.
Follow-up is ongoing.
[0079] FIG. 19A and FIG. 19B One embodiment of spectral domain
optical coherence tomography (SD-OCT) images from the study eye of
subject #1 of cohort 2 (2 implants, 400 .mu.g axitinib in total per
eye) with aflibercept treatment history of 16 months prior to
injection of the implants in the right eye (OD). Sub-retinal fluid
was clearly visible at baseline (pre-treatment). Importantly, the
sub-retinal fluid was gone after 2-3 months after implants
injection and this stage was essentially maintained over 15.5
months (15.5 months shown in FIG. 19B, the earlier visits in FIG.
19A). Best corrected visual acuity (BCVA) was not impaired.
[0080] FIG. 20 One embodiment of spectral domain optical coherence
tomography (SD-OCT) images from subject #7 of cohort 2 (2 implants,
400 .mu.g axitinib in total per eye). Subject #7 who had received
aflibercept for 6 years prior to study start showed significant
reduction in CSFT and no impairment of BCVA for 9 months after
implant injection.
[0081] FIG. 21 One embodiment of spectral domain optical coherence
tomography (SD-OCT) images from subject #1 of cohort 3a (3
implants, 600 .mu.g axitinib in total per eye). A significant
reduction in CSFT was observed at 2 months and maintained for 7.5
months in subject #1 from cohort 3a who was naive for AMD
treatment. BCVA was not impaired.
[0082] FIG. 22 One embodiment of spectral domain optical coherence
tomography (SD-OCT) images from subject #1 from cohort 3b (2
implants, 400 .mu.g axitinib in total per eye including
co-administration of an anti-VEGF agent), who was anti-VEGF
treatment naive. CSFT was rapidly reduced within 7 days and further
reduced and maintained low until month 3.
[0083] FIG. 23 One embodiment of spectral domain optical coherence
tomography (SD-OCT) images from subject #2 from cohort 3b (2
implants, 400 .mu.g axitinib in total per eye including initial
co-administration of an anti-VEGF agent), who had received
anti-VEGF treatment for 7 months prior to implant injection. CSFT
was rapidly reduced within 7 days. The low CSFT value was
maintained until month 2.
[0084] FIG. 24 One embodiment of the agglomeration tendency of
axitinib when preparing and casting a hydrogel implant according to
an embodiment of the invention using micronized vs. non-micronized
axitinib under otherwise identical conditions.
[0085] FIG. 25A, FIG. 25B and FIG. 25C One embodiment of an
injector according to the present invention for injecting an
implant into the vitreous humor of a patient. This depicted
embodiment of an injector comprises a Hamilton syringe body and a
Nitinol push wire to deploy the implant. FIG. 25A shows the
Hamilton syringe body inside of an injection molded casing. FIG.
25B shows the injection molded casing without the Hamilton syringe
body therein. FIG. 25C shows a schematic view of the components of
this embodiment of the injector.
[0086] FIG. 26A Exploded view diagram of one embodiment of an
injector according to the present invention that is made of an
injection molded body. FIG. 26B shows a photograph of the fully
assembled injector.
[0087] FIG. 26C shows an exploded view of a first assembly of an
injector according to the present invention. FIG. 26D shows an
exploded view of a second assembly of an injector according to the
present invention. FIG. 26E shows that the first and the second
assembly can be aligned. FIG. 26F shows the cowl of the second
assembly being secured to the body of the first assembly. FIG. 26G
shows the needle shield being removed from the cowl of the second
assembly and the plunger clip being removed from the body and
plunger of the first assembly. FIG. 26H shows the plunger of the
first assembly being actuated to deploy the implant from the lumen
of the needle of the second assembly.
[0088] FIG. 27 Phase 1 study design with implants containing 200
.mu.g axitinib according to one embodiment of the invention.
[0089] FIG. 28 Proposed phase 2 study design with an implant
containing 600 .mu.g axitinib according to one embodiment of the
invention.
DEFINITIONS
[0090] The term "implant" as used herein (sometimes also referred
to as "depot") refers to an object that contains an active agent,
specifically a tyrosine kinase inhibitor (TKI) such as axitinib, as
well as other compounds as disclosed herein, and that is
administered into the human or animal body, e.g., to the vitreous
humor of the eye (also called "vitreous chamber" or "vitreous
body") where it remains for a certain period of time while it
releases the active agent into the surrounding environment. An
implant can have any predetermined shape (such as disclosed herein)
before being injected, which shape is maintained to a certain
degree upon placing the implant into the desired location, although
dimensions of the implant (e.g. length and/or diameter) may change
after administration due to hydration as further disclosed herein.
In other words, what is injected into the eye is not a solution or
suspension, but an already shaped, coherent object. The implant has
thus been completely formed as disclosed herein prior to being
administered, and in the embodiments of the present invention is
not created in situ at the desired location in the eye (as would
generally also be possible with suitable formulations). Once
administered, over the course of time the implant is biodegraded
(as disclosed below) in physiological environment, may thereby
change its shape while it decreases in size until it has been
completely dissolved/resorbed. Herein, the term "implant" is used
to refer both to an implant in a hydrated (also referred to herein
as "wet") state when it contains water, e.g. after the implant has
been hydrated or re-hydrated once administered to the eye or
otherwise immersed into an aqueous environment (such as in vitro),
as well as to an implant in its/a dry (dried/dehydrated) state,
i.e., after the implant has been produced and dried and just prior
to being loaded into a needle, or after having been loaded into a
needle as disclosed herein, or wherein the implant has been
manufactured in a dry state without the need for dehydration. Thus,
in certain embodiments, an implant in its dry/dried state in the
context of the present invention may contain no more than about 1%
by weight water. The water content of an implant in its dry/dried
state may be measured e.g. by means of a Karl Fischer coulometric
method. Whenever dimensions of an implant (i.e., length, diameter,
or volume) are reported herein in the hydrated state, these
dimensions are measured after the implant has been immersed in
phosphate-buffered saline at 37.degree. C. for 24 hours. Whenever
dimensions of an implant are reported herein in the dry state,
these dimensions are measured after the implant has been fully
dried (and thus, in certain embodiments, contain no more than about
1% by weight water) and the implant is in a state to be loaded into
a needle for subsequent administration. In certain embodiments, the
implant is kept in an inert atmosphere glove box containing below
20 ppm of both oxygen and moisture for at least about 7 days.
Details of an embodiment of the dimension measurement are reported
in Example 6.1.
[0091] The term "ocular" as used in the present invention refers to
the eye in general, or any part or portion of the eye (as an
"ocular implant" according to the invention can in principle be
administered to any part or portion of the eye) or any disease of
the eye (as in one aspect the present invention generally refers to
treating any diseases of the eye ("ocular diseases"), of various
origin and nature. The present invention in certain embodiments is
directed to intravitreal injection of an ocular implant (in this
case the "ocular implant" is thus an "intravitreal implant"), and
to the treatment of ocular diseases affecting the posterior segment
of the eye, as further disclosed below.
[0092] The term "patient" herein includes both human and animal
patients. The implants according to the present invention are
therefore suitable for human or veterinary medicinal applications.
The patients enrolled and treated in the clinical study reported in
Example 6 are referred to as "subjects". Generally, a "subject" is
a (human or animal) individual to which an implant according to the
present invention is administered, such as during a clinical study.
A "patient" is a subject in need of treatment due to a particular
physiological or pathological condition.
[0093] The term "biodegradable" refers to a material or object
(such as the ocular implant according to the present invention)
which becomes degraded in vivo, i.e., when placed in the human or
animal body. In the context of the present invention, as disclosed
in detail herein below, the implant comprising the hydrogel within
which particles of a TKI such as particles of axitinib, are
dispersed, slowly biodegrades over time once deposited within the
eye, e.g., within the vitreous humor. In certain embodiments
biodegradation takes place at least in part via ester hydrolysis in
the aqueous environment of the vitreous. The implant slowly
dissolves until it is fully resorbed and is no longer visible in
the vitreous.
[0094] A "hydrogel" is a three-dimensional network of hydrophilic
natural or synthetic polymers (as disclosed herein) that can swell
in water and hold an amount of water while maintaining or
substantially maintaining its structure, e.g., due to chemical or
physical cross-linking of individual polymer chains. Due to their
high water content, hydrogels are soft and flexible, which makes
them very similar to natural tissue. In the present invention the
term "hydrogel" is used to refer both to a hydrogel in the hydrated
state when it contains water (e.g. after the hydrogel has been
formed in an aqueous solution, or after the hydrogel has been
(re-)hydrated once implanted into the eye or other part of the body
or otherwise immersed into an aqueous environment) and to a
hydrogel in its dry (dried/dehydrated) state when it has been dried
to a low water content of e.g. not more than 1% by weight. In the
present invention, wherein an active principle is contained (e.g.
dispersed) in a hydrogel, the hydrogel may also be referred to as a
"matrix".
[0095] The term "polymer network" describes a structure formed of
polymer chains (of the same or different molecular structure and of
the same or different molecular weight) that are crosslinked with
each other. The types of polymers suitable for the purposes of the
present invention are disclosed herein. The polymer network may
also be formed with the aid of a crosslinking agent as also
disclosed herein.
[0096] The term "amorphous" refers to a polymer or polymer network
or other chemical substance or entity which does not exhibit
crystalline structures in X-ray or electron scattering
experiments.
[0097] The term "semi-crystalline" refers to a polymer or polymer
network or other chemical substance or entity which possesses some
crystalline character, i.e., exhibits some crystalline properties
in X-ray or electron scattering experiments.
[0098] The term "crystalline" refers to a polymer or polymer
network or other chemical substance or entity which has crystalline
character as evidenced by X-ray or electron scattering
experiments.
[0099] The term "precursor" herein refers to those molecules or
compounds that are reacted with each other and that are thus
connected via crosslinks to form the polymer network and thus the
hydrogel matrix. While other materials might be present in the
hydrogel, such as active agents or buffers, they are not referred
to as "precursors".
[0100] The parts of the precursor molecules that are still present
in the final polymer network are also called "units" herein. The
"units" are thus the building blocks or constituents of the polymer
network forming the hydrogel. For example, a polymer network
suitable for use in the present invention may contain identical or
different polyethylene glycol units as further disclosed
herein.
[0101] The molecular weight of a polymer precursor as used for the
purposes of the present invention and as disclosed herein may be
determined by analytical methods known in the art. The molecular
weight of polyethylene glycol may for example be determined by any
method known in the art, including gel electrophoresis such as
SDS-PAGE (sodium dodecyl sulphate-polyacrylamide gel
electrophoresis), gel permeation chromatography (GPC), including
GPC with dynamic light scattering (DLS), liquid chromatography
(LC), as well as mass spectrometry such as matrix-assisted laser
desorption/ionization-time of flight (MALDI-TOF) spectrometry or
electrospray ionization (ESI) mass spectrometry. The molecular
weight of a polymer, including a polyethylene glycol precursor as
disclosed herein, is an average molecular weight (based on the
polymer's molecular weight distribution), and may therefore be
indicated by means of various average values, including the weight
average molecular weight (Mw) and the number average molecular
weight (Mn). In the case of polyethylene glycol precursors as used
in the present invention, the molecular weight indicated herein is
the number average molecular weight (Mn).
[0102] In certain embodiments of the present invention, the term
"fiber" (used interchangeably herein with the term "rod")
characterizes an object (i.e., in the present case the implant
according to the present invention) that in general has an
elongated shape. Specific dimensions of implants of the present
invention are disclosed herein. The implant may have a cylindrical
or essentially cylindrical shape, or may have a non-cylindrical
shape. The cross-sectional area of the fiber or the implant may be
either round or essentially round, but may in certain embodiments
also be oval or oblong, or may in other embodiments have different
geometries, such as cross-shaped, star-shaped or other as disclosed
herein.
[0103] The term "release" (and accordingly the terms "released",
"releasing" etc.) as used herein refers to the provision of agents
such as an API from an implant of the present invention to the
surrounding environment. The surrounding environment may be an in
vitro or in vivo environment as described herein. In certain
specific embodiments, the surrounding environment is the vitreous
humor and/or ocular tissue, such as the retina and the choroid.
Thus, whenever it is herein stated that the implant "releases" or
"provides for (sustained) release" of a TKI such as axitinib, this
not only refers to the provision of TKI such as axitinib directly
from the implant while the hydrogel has not yet (fully)
biodegraded, but also refers to the continued provision of TKI such
as axitinib to the surrounding environment following full
degradation of the hydrogel when remaining TKI is still present in
this surrounding environment (e.g. in an agglomerated form as
further disclosed herein) for an extended period of time and
continues to exert its therapeutic effect. Accordingly, the
"treatment period" referred to herein (i.e., the period during
which a certain therapeutic effect as described herein is achieved)
may extend to a period of time even after the implant/the hydrogel
has fully biodegraded as further disclosed herein.
[0104] The term "sustained release" is defined for the purposes of
the present invention to refer to products (in the case of the
present invention the products are implants) which are formulated
to make a drug available over an extended period of time, thereby
allowing a reduction in dosing frequency compared to an immediate
release dosage form (such as e.g. a solution of an active principle
that is injected into the eye). Other terms that may be used herein
interchangeably with "sustained release" are "extended release" or
"controlled release". "Sustained release" thus characterizes the
release of an API, specifically, the TKI, such as axitinib, that is
contained in an implant according to the present invention. The
term "sustained release" per se is not associated with or limited
to a particular rate of (in vitro or in vivo) release, although in
certain embodiments of the invention an implant may be
characterized by a certain average rate of (in vitro or in vivo)
release or a certain release profile as disclosed herein. As an
implant of the present invention (whether explicitly referred to
herein as a "sustained release" implant or simply as an "implant")
provides for sustained release of the API, an implant of the
present invention may therefore also be referred to as a
"depot".
[0105] Whenever it is stated herein that a certain administration
or injection is performed "concurrently with" or "simultaneously
to" or "at the same time as" an administration or injection of an
implant according to the present invention, this means that the
respective injection of either two or more implants or the
injection of one or more implant(s) together with the injection of
a suspension or solution e.g. of an anti-VEGF agent as disclosed
herein is normally performed immediately one after the other, i.e.,
without any significant delay. For example, if a total dose of
about 400 .mu.g axitinib is to be administered to one eye and that
total dose is comprised in two implants according to the invention,
each containing about 200 .mu.g of axitinib, these two implants are
normally injected into the vitreous chamber immediately one after
the other within the same treatment session, of course by
respecting all precautions for a safe and precise injection at the
desired site, but without any unnecessary delay. The same applies
to the administration of one or more implant(s) according to the
present invention concurrently with/simultaneously to/at the same
time with the administration of an additional anti-VEGF agent as
described herein. In case the additional anti-VEGF agent is
administered by an intravitreal injection of a suspension or
solution containing the anti-VEGF agent, this injection is also
normally intended to take place immediately (as disclosed above)
before or after the intravitreal injection of the one or more
implant(s) according to the present invention, i.e., ideally during
one treatment session.
[0106] However, under specific circumstances, e.g. in case
complications during the administration of the first implant are
experienced and/or the physician carrying out the injection
concludes that a second injection during the same session on the
same day, or within the following days, may not be advisable, the
second implant may also be administered e.g. one or two weeks after
the first implant. Since, as will be disclosed in more detail
herein, the implants may persist in the vitreous of a human eye for
a duration of an extended period of time, such as for about 9 to
about 12 months, the administration of two implants e.g. one or two
weeks apart is still regarded as "concurrently" in the context of
the present invention. Similar considerations apply for the
"concurrent" administration of an implant according to the present
invention and an anti-VEGF agent. Thus, an anti-VEGF agent can be
administered concurrently, i.e., at or around the same time as
described herein, with the intravitreal administration of an
implant of the present invention.
[0107] In certain other embodiments, however, an anti-VEGF agent
can also be administered in combination with an intravitreal
implant of the present invention such that the anti-VEGF agent is
administered later, such as 1 month or 2 months or 3 months after
the intravitreal injection of an implant according to the present
invention.
[0108] The term "rescue medication" generally refers to a
medication that may be administered to a patient under pre-defined
conditions (e.g. during a study in case a patient does not
sufficiently respond to investigational treatment), or to manage an
emergency situation. The conditions for administering rescue
medication in the clinical study disclosed in Example 6 herein are
indicated under the sub-heading "Rescue medication" in the
description of Example 6 (for % rescue medication administration,
see in particular Table 27). In certain embodiments of the present
invention, "rescue medication" refers to one dose of an anti-VEGF
agent as disclosed herein, administered as an intravitreal
injection of a solution or suspension of the anti-VEGF agent. In
certain specific embodiments, the rescue medication is one dose (2
mg) aflibercept administered by means of intravitreal
injection.
[0109] As used herein, the term "about" in connection with a
measured quantity, refers to the normal variations in that measured
quantity, as expected by one of ordinary skill in the art in making
the measurement and exercising a level of care commensurate with
the objective of measurement and the precision of the measuring
equipment.
[0110] The term "at least about" in connection with a measured
quantity refers to the normal variations in the measured quantity,
as expected by one of ordinary skill in the art in making the
measurement and exercising a level of care commensurate with the
objective of measurement and precisions of the measuring equipment
and any quantities higher than that.
[0111] The term "average" as used herein refers to a central or
typical value in a set of data (points), which is calculated by
dividing the sum of the data (points) in the set by their number
(i.e., the mean value of a set of data).
[0112] As used herein, the singular forms "a," "an", and the
include plural references unless the context clearly indicates
otherwise.
[0113] The term "and/or" as used in a phrase such as "A and/or B"
herein is intended to include both "A and B" and "A or B".
[0114] Open terms such as "include," "including," "contain,"
"containing" and the like as used herein mean "comprising" and are
intended to refer to open-ended lists or enumerations of elements,
method steps, or the like and are thus not intended to be limited
to the recited elements, method steps or the like but are intended
to also include additional, unrecited elements, method steps or the
like.
[0115] The term "up to" when used herein together with a certain
value or number is meant to include the respective value or
number.
[0116] The terms "from A to B", "of from A to B", and "of A to B"
are used interchangeably herein and all refer to a range from A to
B, including the upper and lower limits A and B.
[0117] The terms "API", "active (pharmaceutical) ingredient",
"active (pharmaceutical) agent", "active (pharmaceutical)
principle", "(active) therapeutic agent", "active", and "drug" are
used interchangeably herein and refer to the substance used in a
finished pharmaceutical product (FPP) as well as the substance used
in the preparation of such a finished pharmaceutical product,
intended to furnish pharmacological activity or to otherwise have
direct effect in the diagnosis, cure, mitigation, treatment or
prevention of a disease, or to have direct effect in restoring,
correcting or modifying physiological functions in a patient.
[0118] In certain embodiments, the TKI used according to the
present invention is axitinib. Axitinib is the active ingredient in
INLYTA.RTM. (Pfizer, NY), indicated for the treatment of advanced
renal cell carcinoma. It is a small molecule (386.47 Daltons)
synthetic tyrosine kinase inhibitor. The primary mechanism of
action is inhibition of angiogenesis (the formation of new blood
vessels) by inhibition of receptor tyrosine kinases, primarily:
VEGFR-1, VEGFR-2, VEGFR-3, PDGFR-.beta. and c-Kit (Keating.
Axitinib: a review in advanced renal cell carcinoma. 2015, Drugs,
75(16):1903-13; Kernt et al., Inhibitory activity of ranibizumab,
sorafenib, and pazopanib on light-induced overexpression of
platelet-derived growth factor and vascular endothelial growth
factor A and the vascular endothelial growth factor receptors 1 and
2 and neuropilin 1 and 2. 2012, Retina, 32(8):1652-63), which are
involved in pathologic angiogenesis, tumor growth, and cancer
progression. Axitinib is therefore a multi-target inhibitor that
inhibits both VEGF and PDGF pathways.
[0119] The molecular formula of axitinib is
C.sub.22H.sub.18N.sub.4OS, and its IUPAC name is
N-methyl-2-[3-((E)-2-pyridin-2-yl-vinyl)-1H-indazol-6-ylsulfanyl]-benzami-
de. It has the following chemical structure:
##STR00001##
[0120] The solubility of axitinib in biorelevant media (PBS, pH 7.2
at 37.degree. C.) has been determined to be low, approximately 0.4
to 0.5 .mu.g/mL. Its partition coefficient (n-octanol/water) is 4.2
(logP; cf. DrugBank entry "axitinib").
[0121] For the purposes of the present invention, active agents
(including axitinib) in all their possible forms, including any
active agent polymorphs or any pharmaceutically acceptable salts,
anhydrates, hydrates, other solvates or derivatives of active
agents, can be used. Whenever in this description or in the claims
an active agent is referred to by name, e.g., "axitinib", even if
not explicitly stated, it also refers to any such polymorphs,
pharmaceutically acceptable salts, anhydrates, solvates (including
hydrates) or derivatives of the active agent.
[0122] The term "polymorph" as used herein refers to any
crystalline form of an active agent such as axitinib. Frequently,
active agents that are solid at room temperature exist in a variety
of different crystalline forms, i.e, polymorphs, with one polymorph
being the thermodynamically most stable at a given temperature and
pressure.
[0123] With respect to axitinib, suitable solid forms and
polymorphs of axitinib including anhydrous forms and solvates are
for example disclosed in A. M. Campeta et al., Journal of
Pharmaceutical Sciences, Vol. 99, No. 9, September 2010, 3874-3886.
All axitinib polymorphs (whether anhydrous forms or solvates) can
be used for preparing implants according to certain embodiments of
the present invention, including the most thermodynamically stable
polymorph of axitinib referred to as XLI in e.g. U.S. Pat. No.
8,791,140 B2. XLI is an anhydrous crystalline form of axitinib. In
certain embodiments of the invention, the axitinib used for
preparing the implants according to the present invention is the
anhydrous crystalline form XLI. In certain other embodiments,
crystalline anhydrous forms of axitinib that are suitable for use
in the present invention include (but are not limited to)
polymorphs I, IV, VI, and XXV. In addition to the anhydrous forms,
there exist numerous solvates of axitinib with various solvents, as
also described in the cited art, which also can all be used for
preparing implants according to the present invention. All the
above-mentioned forms are well-characterized and described in the
art, such as in the paper by Campeta et al. cited above, or in the
patent literature, including, but not limited to U.S. Pat. No.
8,791,140 B2, US 2006/0094763, and WO 2016/178150 A1. Any of the
axitinib polymorphic forms known and disclosed in the art,
specifically (but not limited to) the references cited herein, may
be used in the present invention.
[0124] In certain specific embodiments, the axitinib used for
preparing the implants according to the present invention and/or
present in the implants according to the present invention is
characterized by an XRD pattern comprising at least five
characteristic 20 peaks selected from 8.3, 9.3, 13.7, 15.6, 16.1,
16.5, 17.6, 18.6, 21.0, 22.6, 23.1, 23.4, 24.1, and 26.0, each
value+0.2 2.theta..degree.. Particularly, axitinib used for
preparing the implants according to the present invention and/or
present in the implants according to the present invention is
characterized by an XRD pattern comprising at least five
characteristic 2.theta..degree. peaks selected from 8.3, 9.3, 15.6,
16.5, 17.6, 21.0, 24.1 and 26.0, each value+0.2 2.theta..degree.,
and/or .sup.13C NMR in DMSO solvent comprising chemical shifts at
26.1, 114.7, 154.8 and 167.8, each shift+0.2 ppm, and/or .sup.13C
solid state NMR comprising chemical shifts at 171.1, 153.2, 142.6,
139.5, 131.2, 128.1 and 126.3, each shift+0.2 ppm, and/or
characterized by a DSC isotherm comprising two endothermic peaks
ranging between 213.degree. C. to 217.degree. C. (Peak 1) and
219.degree. C. to 224.degree. C. (Peak 2). In one specific
embodiment, the non-solvated crystalline form SAB-I of axitinib
disclosed in WO 2016/178150 may be used for preparing the implants
according to the present invention.
[0125] Axitinib inhibits VEGF signaling and it also inhibits PDGF
signaling. In addition to inhibiting VEGF/PDGF, it inhibits c-kit,
a survival factor for developing blood vessels with a clearance
half-life (t.sub.1/2) of a few hours (Rugo et al., Phase I trial of
the oral antiangiogenesis agent AG-013736 in patients with advanced
solid tumors. 2005, J clin Oncol., 23(24):5474-83), whereas
ranibizumab and aflibercept each have t.sub.1/2 of several days in
the human eye. Longer t.sub.1/2 of these large molecule antibodies
enable them to maintain efficacious tissue concentrations for
weeks, whereas small molecules are cleared more quickly. However,
due to the low solubility of axitinib and its inclusion in the
hydrogel implant of the present invention which remains in the
vitreous humor (VH) for an extended period of time, such as for
months, therapeutically effective amounts of axitinib are delivered
over the period the implant persists in the VH. Therefore,
intravitreal sustained delivery of axitinib provides a multi-target
inhibitor that can in principle inhibit both VEGF and PDGF pathways
without the need of combination therapies and without the need for
frequent intravitreal injections.
[0126] As used herein, the term "therapeutically effective" refers
to the amount of drug or active agent needed to produce a certain
desired therapeutic result after administration. For example, in
the context of the present invention, one desired therapeutic
result would be the reduction of the central subfield thickness
(CSFT) as measured by optical coherence tomography in a patient
suffering from neovascular AMD as patients suffering from
neovascular AMD have elevated CSFT. A "therapeutically effective"
amount of an active agent in the context of the present invention
may also be a multiple of the IC.sub.50 this active agent provides
against a particular substrate, such as 50 or more times the
IC.sub.50. For example, IC.sub.50 values of the TKI axitinib
against angiogenesis-related RTKs are presented in Table 12.
[0127] The abbreviation "PBS" when used herein means
phosphate-buffered saline.
[0128] The abbreviation "PEG" when used herein means polyethylene
glycol.
DETAILED DESCRIPTION
I. The Implant
The Active Principle:
[0129] One aspect of the present invention is a sustained release
biodegradable ocular implant comprising a hydrogel and at least
about 150 .mu.g of a tyrosine kinase inhibitor (TKI), wherein TKI
particles are dispersed within the hydrogel. In one embodiment, the
present invention provides a sustained release biodegradable ocular
implant comprising a hydrogel and at least about 150 .mu.g of a
tyrosine kinase inhibitor (TKI), wherein TKI particles are
dispersed within the hydrogel, and wherein the implant in its dry
state has a length of less than about 17 mm.
[0130] The active principle contained in an implant of this aspect
of the invention is a TKI. Examples for suitable TKIs are axitinib,
sorafenib, sunitinib, nintedanib, pazopanib, regorafenib,
cabozantinib, and vandetanib. In particular embodiments, the TKI
used in this and other aspects of the present invention is
axitinib. Details on axitinib, its chemical structure, polymorphs,
solvates, salts etc. and its properties such as solubility are
provided above in the definitions section.
[0131] All features (individually or any combinations of features)
disclosed herein with respect to an implant according to the
present invention may be used to characterize the sustained release
biodegradable ocular implant comprising a hydrogel and at least
about 150 .mu.g of a tyrosine kinase inhibitor (TKI), wherein TKI
particles are dispersed within the hydrogel, and wherein the
implant in its dry state has a length of less than about 17 mm.
[0132] In particular embodiments, the implant of the invention is
an intravitreal implant, i.e., is administered to the vitreous
humor (also referred to herein as "administered
intravitreally").
[0133] The TKI, such as axitinib, is contained in the implant of
the invention in a range of doses as disclosed herein of at least
150 .mu.g, such as from about 150 .mu.g to about 1800 .mu.g, from
about 150 .mu.g to about 1200 .mu.g, or from about 200 .mu.g to
about 800 .mu.g. Any TKI, such as axitinib, amount within these
ranges may be used, such as about 150 .mu.g, about 200 .mu.g, about
300 .mu.g, about 400 .mu.g, about 500 .mu.g, about 600 .mu.g, about
700 .mu.g, about 800 .mu.g, about 900 .mu.g, about 1000 .mu.g,
about 1100 .mu.g or about 1200 .mu.g. In alternative embodiments,
the dose of TKI contained in an implant of the invention, such as
axitinib, may also be up to about 1800 .mu.g, such as about 1300
.mu.g, about 1400 .mu.g, about 1500 .mu.g, about 1600 .mu.g, about
1700 .mu.g, or about 1800 .mu.g. In further alternative
embodiments, the dose of TKI contained in an implant of the
invention, such as axitinib, may be even higher than about 1800
.mu.g or higher than about 2000 .mu.g, such as up to about 3000
.mu.g, up to about 6000 .mu.g, or up to about 10000 .mu.g. All
mentioned values also include a variance of +25% and -20%, or a
variance of +/-10%.
[0134] In certain particular embodiments, the doses of axitinib
contained in an implant of the invention are: [0135] a range from
about 160 .mu.g to about 250 .mu.g, or from about 180 .mu.g to
about 220 .mu.g, or about 200 .mu.g (i.e., including a variance of
+25% and -20%, or a variance of +/-10% of 200 .mu.g) [0136] a range
from about 320 .mu.g to about 500 .mu.g, or from about 360 .mu.g to
about 440 .mu.g, or about 400 .mu.g (i.e., including a variance of
+25% and -20%, or a variance of +/-10% of 400 .mu.g) [0137] a range
from about 375 .mu.g to about 600 .mu.g, or from about 450 .mu.g to
about 550 .mu.g, or about 500 .mu.g (i.e., including a variance of
+25% and -20%, or a variance of +/-10% of 500 .mu.g) [0138] a range
from about 480 .mu.g to about 750 .mu.g, or from about 540 .mu.g to
about 660 .mu.g, or about 600 .mu.g (i.e., including a variance of
+25% and -20%, or a variance of +/-10% of 600 .mu.g) [0139] a range
from about 640 .mu.g to about 1000 .mu.g, or from about 720 .mu.g
to about 880 .mu.g, or about 800 .mu.g (i.e., including a variance
of +25% and -20%, or a variance of +/-10% of 800 .mu.g) [0140] a
range from about 800 .mu.g to about 1250 .mu.g, or from about 900
.mu.g to about 1100 .mu.g, or about 1000 .mu.g (i.e., including a
variance of +25% and -20%, or a variance of +/-10% of 1000 .mu.g)
[0141] a range from about 960 .mu.g to about 1500 .mu.g, or from
about 1080 .mu.g to about 1320 .mu.g, or about 1200 .mu.g (i.e.,
including a variance of +25% and -20%, or a variance of +/-10% of
1200 .mu.g) [0142] a range from about 1440 .mu.g to about 2250
.mu.g, or from about 1620 .mu.g to about 1980 .mu.g, or about 1800
.mu.g (i.e., including a variance of +25% and -20%, or a variance
of +/-10% of 1800 .mu.g).
[0143] In one preferred embodiment, the dose of axitinib contained
in one implant of the invention is from about 480 .mu.g to about
750 .mu.g, or from about 540 .mu.g to about 660 .mu.g, or in
particular embodiments is about 600 .mu.g.
[0144] The disclosed amounts of TKI, such as axitinib, including
the mentioned variances, refer to both the final content of the
active principle in the implant, as well as to the amount of active
principle used as a starting component per implant when
manufacturing the implant.
[0145] As will be disclosed in more detail herein below and as will
become apparent from the Examples section, in certain embodiments
of the invention the total dose of the TKI, such as axitinib, to be
administered to a patient, may be contained in two, three or more
implants administered concurrently. For example, a dose of about
400 .mu.g of TKI, such as axitinib, may be administered in one
implant containing about 400 .mu.g axitinib, or in two implants
e.g. each containing about 200 .mu.g axitinib and so on. Of course,
one may not only combine two or more identical implants (or
implants containing the identical dose), but also two or more
different implants (or implants containing different doses) in
order to arrive at a desired total dose. In a particular
embodiment, a total axitinib dose of from about 480 .mu.g to about
750 .mu.g, or from about 540 .mu.g to about 660 .mu.g, or of about
600 .mu.g, is contained in one implant and only one such implant is
administered to a patient in need of such treatment in accordance
with the invention. In another embodiment, a total dose of higher
than about 600 .mu.g, such as from about 800 .mu.g to about 1250
.mu.g, or from about 900 .mu.g to about 1100 .mu.g, or of about
1000 .mu.g, or a total dose from about 960 .mu.g to about 1500
.mu.g, or from about 1080 .mu.g to about 1320 .mu.g, or of about
1200 .mu.g, or a total dose from about 1440 .mu.g to about 2250
.mu.g, or from about 1620 .mu.g to about 1980 .mu.g, or of about
1800 .mu.g is contained in one implant and only one such implant is
administered to a patient in need of such treatment in accordance
with the invention. In other embodiments, the total dose
administered to a patient in accordance with the present invention
may be contained in two or more implants (containing the same or
different amounts of API) administered concurrently.
[0146] The TKI, such as axitinib, is contained in the implant of
the inventionand is dispersed or distributed in the hydrogel that
is comprised of a polymer network. In certain embodiments, the
particles are homogeneously or essentially homogeneously dispersed
in the hydrogel. The hydrogel may prevent the particles from
agglomerating and may provide a matrix for the particles which
holds them in the desired location in the eye while slowly
releasing drug.
[0147] In certain embodiments of the invention, the TKI particles
such as the axitinib particles may be microencapsulated. The term
"microcapsule" (also referred to as "microparticle") is sometimes
defined as a roughly spherical particle with a size varying between
e.g. about 50 nm to about 2 mm. Microcapsules have at least one
discrete domain (or core) of active agent encapsulated in a
surrounding material, sometimes also referred to as a shell. One
suitable agent (without limiting the present disclosure to this)
for microencapsulating the TKI, such as the axitinib, for the
purposes of the present invention, is poly (lactic-co-glycolic
acid).
[0148] In other embodiments, the TKI particles such as the axitinib
particles are not microencapsulated and are thus dispersed in the
hydrogel and thus in the implant of the invention as they are,
i.e., without being admixed to or adjoined with or
microencapsulated by another material such as (but not limited to)
poly (lactic-co-glycolic acid).
[0149] In one embodiment, the TKI particles, such as the axitinib
particles, may be micronized particles. In another embodiment, the
TKI particles, such as the axitinib particles, may not be
micronized. Micronization refers to the process of reducing the
average diameter of particles of a solid material. Particles with
reduced diameters may have inter alia higher dissolution and
erosion rates, which increases the bioavailability of active
pharmaceutical ingredients and may have in certain embodiments a
positive impact on release kinetics. Furthermore, micronized
particles may have a reduced tendency to agglomerate during
manufacturing operations (see also FIG. 24). In the composite
materials field, particle size is known to affect the mechanical
properties when combined with a matrix, with smaller particles
providing superior reinforcement for a given mass fraction. Thus, a
hydrogel matrix filled with micronized TKI particles may have
improved mechanical properties (e.g. brittleness, strain to
failure, etc.) compared to a similar mass fraction of larger TKI
particles. Such properties are important in manufacturing, during
implantation, and during degradation of the implant. Micronization
may also promote a more homogeneous distribution of the active
ingredient in the chosen dosage form or matrix. The particle size
distribution can be measured by methods known in the art, including
sieving, laser diffraction or dynamic light scattering. In certain
embodiments of the invention the TKI, such as the axitinib,
particles used in preparing the implants of the present invention
may have a d90 of less than about 100 .mu.m and/or a d50 of less
than about 50 .mu.m, or a d90 of less than about 75 .mu.m and/or a
d50 or less than about 20 .mu.m as determined by laser diffraction.
In specific embodiments, the d90 of the TKI, such as the axitinib,
may be less than about 30 .mu.m, less than about 20 .mu.m as
determined by laser diffraction. In very particular embodiments,
the d90 of the TKI, such as axitinib, is less than about 10 .mu.m
as determined by laser diffraction. In these or other embodiments,
the d50 of the TKI, such as axitinib, particles used in preparing
the implants of the present invention may be less than about 5
.mu.m as determined by laser diffraction. In these or other
embodiments, the d10 of the TKI, such as the axitinib, particles
used in the present invention may be less than about 3 .mu.m as
determined by laser diffraction. In certain embodiments, the d100
of the TKI, such as the axitinib, particles used in the preparation
of the implants of the present invention may be less than about 20
.mu.m as determined by laser diffraction. The "d90" (also referred
to as "D90" herein) value means that 90 volume-% of all particles
within the measured bulk material (which has a certain particle
size distribution) have a particle size below the indicated value.
For example, a d90 particle size of less than about 10 .mu.m means
that 90 volume-% of the particles in the measured bulk material
have a particle size below about 10 .mu.m. Corresponding
definitions apply to other "d" values, such as the "d10", "d50" or
the "d100" values (also referred to herein as the "D10", "D50" and
"D100" values, respectively). In certain other embodiments also
TKI, such as axitinib, particles with diameters above this
specification may be used.
[0150] Micronized TKI such as axitinib particles may be purchased
per specification from the supplier, or may be prepared e.g.
according to the following exemplary procedure for axitinib
(disclosed in WO 2016/183296 A1, Example 13): 1800 mL of sterile
Water For Injection (WFI) is measured into a 2 L beaker and placed
on a stir plate stirring at 600 RPM with a stir bar, creating a
large WFI vortex in the center of the beaker. One 60 mL BD syringe
containing axitinib in ethanol is placed on a syringe pump which is
clamped above the WFI beaker. A hypodermic needle (21 G, BD) is
connected to the syringe and aimed directly into the center of the
vortex for dispensation of the axitinib solution. The syringe pump
is then run at 7.5 mL/min in order to add the axitinib solution
dropwise to the WFI to precipitate micronized axitinib. After
micronization, the axitinib is filtered, e.g. through a 0.2 .mu.m
vacuum filter and rinsed with WFI. After filtration, the axitinib
powder is collected from the filter e.g. by using a spatula and
vacuum dried for an extended period of time, such as for about 12
or about 24 hours, in order to remove excess solvent. Another
exemplary method of micronizing axitinib is disclosed in Example 9
of WO 2017/091749. The described method of micronization is not
limiting, and other methods of micronizing the active agent such as
axitinib may equally be used. The disclosed micronization method
(or other methods) may also be used for other actives than
axitinib.
[0151] Another aspect of the present invention is a sustained
release biodegradable ocular implant comprising a hydrogel and at
least about 150 .mu.g of a tyrosine kinase inhibitor (TKI), wherein
TKI particles are dispersed within the hydrogel, and wherein the
implant in its dry state has a total weight of about 0.2 mg to
about 1.5 mg. In certain embodiments, the TKI is axitinib or
another TKI as disclosed herein.
[0152] In certain embodiments, the total weight (also referred to
herein as "total mass") of an implant according to the present
invention in its dry state may be from about 400 .mu.g to about 1.2
mg. In certain specific embodiments, the total weight of an implant
according to the invention in its dry state may be from about 0.3
mg to about 0.6 mg, such as from about 0.4 mg to about 0.5 mg, or
may be from about 0.8 mg to about 1.1 mg, such as from about 0.9 mg
to about 1.0 mg.
[0153] All features (individually or any combinations of features)
disclosed herein with respect to an implant according to the
present invention may be used to characterize the sustained release
biodegradable ocular implant comprising a hydrogel and at least
about 150 .mu.g of a tyrosine kinase inhibitor (TKI), wherein TKI
particles are dispersed within the hydrogel, and wherein the
implant in its dry state has a total weight of about 0.2 mg to
about 1.5 mg.
The Polymer Network:
[0154] In certain embodiments, the hydrogel may be formed from
precursors having functional groups that form crosslinks to create
a polymer network. These crosslinks between polymer strands or arms
may be chemical (i.e., may be covalent bonds) and/or physical (such
as ionic bonds, hydrophobic association, hydrogen bridges etc.) in
nature.
[0155] The polymer network may be prepared from precursors, either
from one type of precursor or from two or more types of precursors
that are allowed to react. Precursors are chosen in consideration
of the properties that are desired for the resultant hydrogel.
There are various suitable precursors for use in making the
hydrogels. Generally, any pharmaceutically acceptable and
crosslinkable polymers forming a hydrogel may be used for the
purposes of the present invention. The hydrogel and thus the
components incorporated into it, including the polymers used for
making the polymer network, should be physiologically safe such
that they do not elicit e.g. an immune response or other adverse
effects. Hydrogels may be formed from natural, synthetic, or
biosynthetic polymers.
[0156] Natural polymers may include glycosaminoglycans,
polysaccharides (e.g. dextran), polyaminoacids and proteins or
mixtures or combinations thereof.
[0157] Synthetic polymers may generally be any polymers that are
synthetically produced from a variety of feedstocks by different
types of polymerization, including free radical polymerization,
anionic or cationic polymerization, chain-growth or addition
polymerization, condensation polymerization, ring-opening
polymerization etc. The polymerization may be initiated by certain
initiators, by light and/or heat, and may be mediated by
catalysts.
[0158] Generally, for the purposes of the present invention one or
more synthetic polymers of the group comprising one or more units
of polyalkylene glycol, such as polyethylene glycol (PEG),
polypropylene glycol, poly(ethylene glycol)-block-poly(propylene
glycol) copolymers, or polyethylene oxide, polypropylene oxide,
polyvinyl alcohol, poly (vinylpyrrolidinone), polylactic acid,
polylactic-co-glycolic acid, random or block copolymers or
combinations/mixtures of any of these can be used, while this list
is not intended to be limiting.
[0159] To form covalently crosslinked polymer networks, the
precursors may be covalently crosslinked with each other. In
certain embodiments, precursors with at least two reactive centers
(for example, in free radical polymerization) can serve as
crosslinkers since each reactive group can participate in the
formation of a different growing polymer chain.
[0160] The precursors may have biologically inert and hydrophilic
portions, e.g., a core. In the case of a branched polymer, a core
refers to a contiguous portion of a molecule joined to arms that
extend from the core, where the arms carry a functional group,
which is often at the terminus of the arm or branch. Multi-armed
PEG precursors are examples of such precursors and are further
disclosed herein below.
[0161] Thus a hydrogel for use in the present invention can be made
e.g. from one multi-armed precursor with a first (set of)
functional group(s) and another multi-armed precursor having a
second (set of) functional group(s). By way of example, a
multi-armed precursor may have hydrophilic arms, e.g., polyethylene
glycol units, terminated with primary amines (nucleophile), or may
have activated ester end groups (electrophile). The polymer network
according to the present invention may contain identical or
different polymer units crosslinked with each other.
[0162] Certain functional groups can be made more reactive by using
an activating group. Such activating groups include (but are not
limited to) carbonyldiimidazole, sulfonyl chloride, aryl halides,
sulfosuccinimidyl esters, N-hydroxysuccinimidyl ester, succinimidyl
ester, epoxide, aldehyde, maleimides, imidoesters, acrylates and
the like. The N-hydroxysuccinimide esters (NHS) are useful groups
for crosslinking of nucleophilic polymers, e.g., primary
amine-terminated or thiol-terminated polyethylene glycols. An
NHS-amine crosslinking reaction may be carried out in aqueous
solution and in the presence of buffers, e.g., phosphate buffer (pH
5.0-7.5), triethanolamine buffer (pH 7.5-9.0), borate buffer (pH
9.0-12), or sodium bicarbonate buffer (pH 9.0-10.0).
[0163] In certain embodiments, each precursor may comprise only
nucleophilic or only electrophilic functional groups, so long as
both nucleophilic and electrophilic precursors are used in the
crosslinking reaction. Thus, for example, if a crosslinker has only
nucleophilic functional groups such as amines, the precursor
polymer may have electrophilic functional groups such as
N-hydroxysuccinimides. On the other hand, if a crosslinker has
electrophilic functional groups such as sulfosuccinimides, then the
functional polymer may have nucleophilic functional groups such as
amines or thiols. Thus, functional polymers such as proteins, poly
(allyl amine), or amine-terminated di- or multifunctional
poly(ethylene glycol) can be also used to prepare the polymer
network of the present invention.
[0164] In one embodiment a first reactive precursor has about 2 to
about 16 nucleophilic functional groups each (termed
functionality), and a second reactive precursor allowed to react
with the first reactive precursor to form the polymer network has
about 2 to about 16 electrophilic functional groups each. Reactive
precursors having a number of reactive (nucleophilic or
electrophilic) groups as a multiple of 4, thus for example 4, 8 and
16 reactive groups, are particularly suitable for the present
invention. Any number of functional groups, such as including any
of 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, or 16 groups, is
possible for precursors to be used in accordance with the present
invention, while ensuring that the functionality is sufficient to
form an adequately crosslinked network.
PEG Hydrogels:
[0165] In a certain embodiments of the present invention, the
polymer network forming the hydrogel contains polyethylene glycol
(PEG) units. PEGs are known in the art to form hydrogels when
crosslinked, and these PEG hydrogels are suitable for
pharmaceutical applications e.g. as matrix for drugs intended to be
administered to all parts of the human or animal body.
[0166] The polymer network of the hydrogel implants of the present
invention may comprise one or more multi-arm PEG units having from
2 to 10 arms, or 4 to 8 arms, or 4, 5, 6, 7 or 8 arms. The PEG
units may have a different or the same number of arms. In certain
embodiments, the PEG units used in the hydrogel of the present
invention have 4 and/or 8 arms. In certain particular embodiments,
a combination of 4- and 8-arm PEG units is utilized.
[0167] The number of arms of the PEG used contributes to
controlling the flexibility or softness of the resulting hydrogel.
For example, hydrogels formed by crosslinking 4-arm PEGs are
generally softer and more flexible than those formed from 8-arm
PEGs of the same molecular weight. In particular, if stretching the
hydrogel prior to or after drying as disclosed herein below in the
section relating to the manufacture of the implant is desired, a
more flexible hydrogel may be used, such as a 4-arm PEG, optionally
in combination with another multi-arm PEG, such as an 8-arm PEG as
disclosed above.
[0168] In certain embodiments of the present invention,
polyethylene glycol units used as precursors have an average
molecular weight in the range from about 2,000 to about 100,000
Daltons, or in a range from about 10,000 to about 60,000 Daltons,
or in a range from about 15,000 to about 50,000 Daltons. In certain
particular embodiments the polyethylene glycol units have an
average molecular weight in a range from about 10,000 to about
40,000 Daltons, or of about 20,000 Daltons. PEG precursors of the
same average molecular weight may be used, or PEG precursors of
different average molecular weight may be combined with each other.
The average molecular weight of the PEG precursors used in the
present invention is given as the number average molecular weight
(Mn), which, in certain embodiments, may be determined by
MALDI.
[0169] In a 4-arm PEG, each of the arms may have an average arm
length (or molecular weight) of the total molecular weight of the
PEG divided by 4. A 4a20kPEG precursor, which is one precursor that
can be utilized in the present invention thus has 4 arms with an
average molecular weight of about 5,000 Daltons each. An 8a20k PEG
precursor, which may be used in addition to the 4a20kPEG precursor
in the present invention, thus has 8 arms each having an average
molecular weight of 2,500 Daltons. Longer arms may provide
increased flexibility as compared to shorter arms. PEGs with longer
arms may swell more as compared to PEGs with shorter arms. A PEG
with a lower number of arms also may swell more and may be more
flexible than a PEG with a higher number of arms. In certain
particular embodiments, combinations of PEG precursors with
different numbers of arms, such as a combination of a 4-arm PEG
precursor and an 8-arm precursor, may be utilized in the present
invention. In addition, longer PEG arms have higher melting
temperatures when dry, which may provide more dimensional stability
during storage. For example, an 8-arm PEG with a molecular weight
of 15,000 Dalton crosslinked with trilysine may not be able to
maintain a stretched configuration at room temperature, whereas a
4-arm 20,000 Dalton PEG crosslinked with an 8-arm 20,000 Dalton PEG
may be dimensionally stable in a stretched configuration at room
temperature.
[0170] When referring to a PEG precursor having a certain average
molecular weight, such as a 15kPEG- or a 20kPEG-precursor, the
indicated average molecular weight (i.e., a Mn of 15,000 or 20,000,
respectively) refers to the PEG part of the precursor, before end
groups are added ("20k" here means 20,000 Daltons, and "15k" means
15,000 Daltons--the same abbreviation is used herein for other
average molecular weights of PEG precursors). In certain
embodiments, the Mn of the PEG part of the precursor is determined
by MALDI. The degree of substitution with end groups as disclosed
herein may be determined by means of .sup.1H-NMR after end group
functionalization.
[0171] In certain embodiments, electrophilic end groups for use
with PEG precursors for preparing the hydrogels of the present
invention are N-hydroxysuccinimidyl (NHS) esters, including but not
limited to: "SAZ" referring to a succinimidylazelate end group,
"SAP" referring to a succinimidyladipate end group, "SG" referring
to a succinimidylglutarate end group, and "SS" referring to a
succinimidylsuccinate end group.
[0172] In certain embodiments, nucleophilic end groups for use with
PEG precursors for preparing the hydrogels of the present invention
are amine (denoted as "NH.sub.2") end groups. Thiol (--SH) end
groups or other nucleophilic end groups are also possible.
[0173] In certain preferred embodiments, 4-arm PEGs with an average
molecular weight of about 20,000 Daltons and an electrophilic end
group as disclosed above and 8-arm PEGs also with an average
molecular weight of about 20,000 Daltons and with a nucleophilic
end group as disclosed above are crosslinked for forming the
polymer network and thus the hydrogel according to the present
invention.
[0174] Reaction of nucleophilic group-containing PEG units and
electrophilic group-containing PEG units, such as amine end-group
containing PEG units and activated ester-group containing PEG
units, results in a plurality of PEG units being crosslinked by a
hydrolyzable linker having the formula:
##STR00002##
wherein m is an integer from 0 to 10, and specifically is 1, 2, 3,
4, 5, 6, 7, 8, 9, or 10. In one particular embodiment, m is 6, e.g.
in the case a SAZ-end group-containing PEG is used. For a SAP-end
group, m would be 3, for a SG-end group, m would be 2 and for an
SS-end group m would be 1. All crosslinks within the polymer
network may be the same, or may be different.
[0175] In certain preferred embodiments, the SAZ end group is
utilized in the present invention. This end group may provide for
increased duration in the eye, and the implant of certain
embodiments of the present invention comprising a hydrogel
comprising PEG-SAZ units is biodegraded in the eye, such as in the
vitreous humor of a human eye, only after an extended period of
time, e.g., 9 to 12 months as further disclosed below, and may in
certain circumstance persist even longer. The SAZ group is more
hydrophobic than e.g. the SAP-, SG- or SS-end groups because of a
higher number of carbon atoms in the chain (m being 6, and the
total of carbon atoms between the amide group and the ester group
being 7).
[0176] In certain preferred embodiments, a 4-arm 20,000 Dalton PEG
precursor is combined with an 8-arm 20,000 Dalton PEG precursor,
such as a 4-arm 20,000 Dalton PEG precursor having a SAZ group (as
defined above) combined with an 8-arm 20,000 Dalton PEG precursor
having an amine group (as defined above). These precursors are also
abbreviated herein as 4a20kPEG-SAZ and 8a20kPEG-NH.sub.2,
respectively. The chemical structure of 4a20kPEG-SAZ is:
##STR00003##
wherein R represents a pentaerythritol core structure. The chemical
structure of 8a20kPEG-NH.sub.2 (with a hexaglycerol core) is:
##STR00004##
In the above formulae, n is determined by the molecular weight of
the respective PEG-arm.
[0177] In certain embodiments, the molar ratio of the nucleophilic
and the electrophilic end groups reacting with each other is about
1:1, i.e., one amine group is provided per one SAZ group. In the
case of 4a20kPEG-SAZ and 8a20kPEG-NH.sub.2 this results in a weight
ratio of about 2:1, as the 8-arm PEG contains double the amount of
end groups as the 4-arm PEG. However, an excess of either the
electrophilic (e.g. the NHS end groups, such as the SAZ) end groups
or of the nucleophilic (e.g. the amine) end groups may be used. In
particular, an excess of the nucleophilic, such as the amine-end
group containing precursor may be used, i.e., the weight ratio of
4a20kPEG-SAZ and 8a20kPEG-NH.sub.2 may also be less than 2:1.
[0178] Each and any combination of electrophilic- and
nucleophilic-group containing PEG precursors disclosed herein may
be used for preparing the implant according to the present
invention. For example, any 4-arm or 8-arm PEG-NHS precursor (e.g.
having a SAZ, SAP, SG or SS end group) may be combined with any
4-arm or 8-arm PEG-NH.sub.2 precursor (or any other PEG precursor
having a nucleophilic group). Furthermore, the PEG units of the
electrophilic- and the nucleophilic group-containing precursors may
have the same, or may have a different average molecular
weight.
[0179] Another nucleophilic group-containing crosslinking agent may
be used instead of a PEG-based crosslinking agent. For example, a
low-molecular weight amine linker can be used, such as trilysine
(or a trilysine salt or derivative, such as trilysine acetate) or
other low-molecular weight multi-arm amines.
[0180] In certain embodiments, the nucleophilic group-containing
crosslinking agent may be bound to or conjugated with a
visualization agent. A visualization agent is an agent that
contains a fluorophoric or other visualization-enabling group.
Fluorophores such as fluorescein, rhodamine, coumarin, and cyanine
may for example be used as visualization agents. The visualization
agent may be conjugated with the crosslinking agent e.g. through
some of the nucleophilic groups of the crosslinking agent. Since a
sufficient amount of the nucleophilic groups are necessary for
crosslinking, "conjugated" or "conjugation" in general includes
partial conjugation, meaning that only a part of the nucleophilic
groups are used for conjugation with the visualization agent, such
as about 1% to about 20%, or about 5% to about 10%, or about 8% of
the nucleophilic groups of the crosslinking agent may be conjugated
with a visualization agent. In other embodiments, a visualization
agent may also be conjugated with the polymer precursor, e.g.
through certain reactive (such as electrophilic) groups of the
polymer precursors.
Additional Ingredients:
[0181] The implant of the present invention may contain, in
addition to the polymer units forming the polymer network as
disclosed above and the active principle, other additional
ingredients. Such additional ingredients are for example salts
originating from buffers used during the preparation of the
hydrogel, such as phosphates, borates, bicarbonates, or other
buffer agents such as triethanolamine. In certain embodiments of
the present invention sodium phosphate buffers (specifically, mono-
and dibasic sodium phosphate) are used.
[0182] Optionally, preservatives may be used for the implants of
the present invention. However, in certain embodiments, the
implants of the present invention including the implants containing
axitinib as active agent, are free of preservatives, such as
anti-microbial preservatives (including, but not limited to
benzalkonium chloride (BAK), chlorobutanol, sodium perborate, and
stabilized oxychloro complex (SOC)), or are substantially free of
such preservatives.
[0183] If an in situ gelation is preferred in an embodiment of the
invention, possible additional ingredient may be other agents used
during manufacture of the hydrogel, such as (without being limited
to) viscosity-influencing agents (such as hyaluronic acid etc.),
surfactants etc.
[0184] In certain embodiments, the inserts of the present invention
may contain a visualization agent. Visualization agents that may be
used in the context of the invention are all agents that can be
conjugated with the components of the hydrogel or can be entrapped
within the hydrogel, and that are visible, or may be made visible
when exposed e.g. to light of a certain wavelength, or that are
constrast agents. Suitable visualization agents for use in the
present invention are (but are not limited to) e.g. fluoresceins,
rhodamines, coumarins, cyanines, europium chelate complexes, boron
dipyromethenes, benzofrazans, dansyls, bimanes, acridines,
triazapentalenes, pyrenes and derivatives thereof. A visualization
agent may be conjugated with either the nucleophilic- or the
electrophilic group-containing precursor of which the polymer
network is formed, as disclosed above, or the visualization agent
may be a separate (non-conjugated) agent that is added during the
manufacture of the implant and that is present in the hydrogel.
Formulation:
[0185] In certain embodiments, implants according to the present
invention comprise a TKI, a polymer network made from one or more
polymer precursors as disclosed herein above in the form of a
hydrogel, and optional additional components such as salts etc.
remaining in the implant from the production process (such as
phosphate salts used as buffers etc.). In certain preferred
embodiments, the TKI is axitinib.
[0186] In certain embodiments, the implants according to the
present invention in their dry state may contain from about 15% to
about 80%, such as from about 25% to about 75% by weight TKI and
from about 15% to about 80%, such as from about 20% to about 60% by
weight polymer units, or in particular embodiments from about 35%
to about 65% by weight TKI and from about 25% to about 50% by
weight polymer units (dry composition). In specific embodiments,
the implants according to the present invention may contain from
about 45% to about 55% by weight TKI and from about 37% to about
47% by weight polymer units (dry composition), with the TKI and the
polymer units being selected from those disclosed herein above. In
other specific embodiments, the implants according to the present
invention in their dry state may contain from about 55% to about
75% by weight TKI and from about 20% to about 40% by weight polymer
units (dry composition), with the TKI and the polymer units being
selected from those disclosed herein above. In other specific
embodiments, the implants according to the present invention in
their dry state may contain from about 30% to about 45% by weight
TKI and from about 47% to about 70% by weight polymer units (dry
composition), with the TKI and the polymer units being selected
from those disclosed herein above.
[0187] In one particular embodiment, the implants according to the
present invention in their dry state may contain from about 25% to
about 75% by weight axitinib and from about 20% to about 60% by
weight PEG units, or from about 35% to about 65% by weight axitinib
and from about 25% to about 50% by weight PEG units, or from about
45% to about 55% by weight axitinib and from about 37% to about 47%
by weight PEG units, or from about 48% to about 52% by weight
axitinib and from about 40% to about 44% by weight PEG units (dry
composition). In other particular embodiments, the implants
according to the present invention in their dry state may contain
from about 55% to about 75% by weight axitinib and from about 20%
to about 40% by weight PEG units, or from about 60% to about 75% by
weight axitinib and from about 21% to about 31% by weight PEG units
(dry composition).
[0188] In one further particular embodiment, on a dry weight basis
the axitinib to PEG ratio in an implant according to the invention
may be approximately 50% by weight or more axitinib to
approximately 40% by weight or less PEG, the balance being
phosphate salt. Alternatively, on a dry weight basis the axitinib
to PEG ratio in an implant according to the invention may be from
about 1:1 to about 3:1.
[0189] In certain embodiments, the balance of the implant in its
dried state (i.e., the remainder of the formulation when TKI, such
as axitinib, and polymer hydrogel, such as PEG hydrogel, have
already been taken account of) may be salts remaining from buffer
solutions as disclosed above. In certain embodiments, such salts
are phosphate, borate or (bi) carbonate salts. In one embodiment
the buffer salt is sodium phosphate (mono- and/or dibasic).
[0190] The amounts of the TKI and the polymer(s) may be varied, and
other amounts of the TKI and the polymer hydrogel may be used to
prepare implants according to the invention.
[0191] In certain embodiments, the maximum amount of drug within
the formulation is about two times the amount of the polymer (e.g.,
PEG) units, but may be higher in certain cases, but it is desired
that the mixture comprising, e.g., the precursors, buffers and drug
(in the state before the hydrogel has gelled completely) can be
uniformly cast into a mold or tubing.
[0192] In one embodiment of the invention, the hydrogel after being
formed and prior to being dried, i.e., in a wet state, may comprise
about 3% to about 20% polyethylene glycol representing the
polyethylene glycol weight divided by the fluid weight.times.100.
In one embodiment, the hydrogel in a wet state comprises about 5%
to about 15%, such as about 7.5% to about 15%, or about 5% to about
10% polyethylene glycol representing the polyethylene glycol weight
divided by the fluid weight.times.100.
[0193] In one embodiment of the invention, the wet hydrogel
composition (i.e., after the hydrogel composition has been formed,
i.e., all components forming the hydrogel have been admixed)
comprises from about 5% to about 50% by weight active principle,
such as axitinib, and from about 5% to about 50% or from about 5%
to about 30% by weight PEG units.
[0194] In certain embodiments, a solids content of about 10% to
about 50%, or of about 25% to about 50% (w/v) (wherein "solids"
means the combined weight of polymer precursor(s), salts and the
drug in solution/suspension) may be utilized in the wet
compositionwhen forming the hydrogel for the implants according to
the present invention. Thus, in certain embodiments, the total
solids content of the wet hydrogel composition to be cast into a
mold or tubing in order to shape the hydrogel may be no more than
about 60%, or no more than about 50%, or no more than about 40%,
such as equal to or lower than about 35% (w/v). The content of TKI,
such as axitinib, may be no more than about 40%, or no more than
about 30%, such as equal to or lower than about 25% (w/v) of the
wet composition. The solids content may influence the viscosity and
thus may also influence the castability of the wet hydrogel
composition.
[0195] In certain embodiments, the water content of the hydrogel
implant in its dry (dehydrated/dried) state, e.g. prior to being
loaded into a needle, or when loaded in a needle, may be very low,
such as not more than 1% by weight of water. The water content may
in certain embodiments also be lower than that, possibly not more
than 0.25% by weight or even not more than 0.1% by weight. In the
present invention the term "implant" is used to refer both to an
implant in a hydrated state when it contains water (e.g. after the
implant has been (re-)hydrated once administered to the eye or
otherwise immersed into an aqueous environment) as well as to an
implant in its dry (dried/dehydrated) state, e.g., when it has been
dried to a low water content of e.g. not more than about 1% by
weight or when the preparation results in such a low water content
implant without the necessity of a drying step. In certain
embodiments, an implant in its dry state is an implant that after
production is kept under inert nitrogen atmosphere (containing less
than 20 ppm of both oxygen and moisture) in a glove box for at
least about 7 days prior to being loaded into a needle. The water
content of an implant may be e.g. measured using a Karl Fischer
coulometric method.
[0196] In certain embodiments, the total weight (also referred to
herein as "total mass") of an implant according to the present
invention in its dry state may be from about 200 .mu.g (i.e., 0.2
mg) to about 1.5 mg, or from about 400 .mu.g to about 1.2 mg. In
certain specific embodiments, the total weight of an implant
according to the invention in its dry state may be from about 0.3
mg to about 0.6 mg, such as from about 0.4 mg to about 0.5 mg, e.g.
in case the implant contains axitinib in an amount of from about
160 .mu.g to about 250 .mu.g. In certain other specific
embodiments, the total mass of an implant according to the
invention in its dry state may be from about 0.75 mg to about 1.25
mg, or from about 0.8 mg to about 1.1 mg, or from about 0.9 mg to
about 1.0 mg, e.g. in case the implant contains axitinib in an
amount of from about 480 .mu.g to about 750 .mu.g.
[0197] In certain embodiments, an implant according to the present
invention in its dry state may contain from about 200 .mu.g to
about 1000 .mu.g TKI, such as axitinib, per mm.sup.3 (i.e., per 1
mm.sup.3 volume of the dry implant). In certain specific
embodiments, an implant according to the present invention in its
dry state may contain from about 200 .mu.g to about 300 .mu.g
axitinib per mm.sup.3, e.g. in case the implant contains axitinib
in an amount of from about 160 .mu.g to about 250 .mu.g. In certain
other specific embodiments, an implant according to the present
invention in its dry state may contain from about 500 .mu.g to
about 800 .mu.g axitinib per mm.sup.3, e.g. in case the implant
contains axitinib in an amount of from about 480 .mu.g to about 750
.mu.g.
[0198] The implants of the present invention may thus have
different densities. The densities of the final implants (i.e., in
their dry state) may be controlled and determined by various
factors, including but not limited to the concentration of the
ingredients in the wet composition when forming the hydrogel, and
certain conditions during manufacturing of the implant. For
example, the density of the final implant in certain embodiments
can be increased by means of sonication or degassing, e.g. using
vacuum, at certain points during the manufacturing process.
[0199] In certain embodiments, implants according to the invention
contain a therapeutically effective amount of TKI such as axitinib
for release over an extended period of time, but are nevertheless
relatively small in length and/or diameter. This is advantageous
both in terms of ease of administration (injection) as well as in
terms of reducing possible damage to ocular tissue and reducing a
possible impact of the patient's vision while the implant is in
place. The implants of the present invention combine the benefits
of a suitably high dose of the TKI (i.e., a therapeutically
effective dose adjusted to a particular patient's need) with a
relatively small implant size.
[0200] Exemplary implants according to the invention are disclosed
in the Examples section, in Tables 1, 6, 21.1, 21.2, and 29
(including prophetic examples of implants according to the
invention containing a high amount of TKI which are disclosed in
Table 29).
Dimensions of the Implant and Dimensional Change Upon Hydration
Through Stretching:
[0201] The dried implant may have different geometries, depending
on the method of manufacture, such as the use of mold or tubing
into which the mixture comprising the hydrogel precursors including
the TKI is cast prior to complete gelling. The implant according to
the present invention is also referred as a "fiber" (which term is
used interchangeably herein with the term "rod"), wherein the fiber
is an object that has in general an elongated shape. The implant
(or the fiber) may have different geometries, with specific
dimensions as disclosed herein.
[0202] In one embodiment, the implant is cylindrical or has an
essentially cylindrical shape. In this case, the implant has a
round or an essentially round cross-section.
[0203] In other embodiments of the invention, the implant is
non-cylindrical, wherein the implant is optionally elongated in its
dry state, wherein the length of the implant is greater than the
width of the implant, wherein the width is the largest cross
sectional dimension that is substantially perpendicular to the
length. In certain embodiments, the width may be about 0.1 mm to
about 0.5 mm. Various geometries of the outer implant shape or its
cross-section may be used in the present invention. For example,
instead of a round diameter fiber (i.e., a cylindrical implant), a
cross-shaped fiber (i.e., wherein the cross-sectional geometry is
cross-like) may be used. Other cross-sectional geometries, such as
oval or oblong, rectangular, triangular, star-shaped etc. may
generally be used. In certain embodiments, the fiber may also be
twisted. In embodiments where the implant is administered to the
eye by means of a needle, the dimensions of the implant (i.e., its
length and diameter) and its cross-sectional geometry must be such
as to enable loading the implant into the needle, particularly a
fine-diameter needle such as a 25-gauge or 27-gauge needle as
further disclosed herein.
[0204] The polymer network, such as the PEG network, of the
hydrogel implant according to certain embodiments of the present
invention may be semi-crystalline in the dry state at or below room
temperature, and amorphous in the wet state. Even in the stretched
form, the dry implant may be dimensionally stable at or below room
temperature, which may be advantageous for loading the implant into
the needle and for quality control.
[0205] Upon hydration of the implant in the eye (which can be
simulated by immersing the implant into PBS, pH 7.2 at 37.degree.
C.) the dimensions of the implant according to the invention may
change: generally, the diameter of the implant may increase, while
its length may decrease or at least may stay essentially the same.
An advantage of this dimensional change is that, while the implant
in its dry state is sufficiently thin to be loaded into a fine
diameter needle (such as a 25-, or 27-, or in some cases even a
smaller diameter needle, such as a 30-gauge needle) to be injected
into the eye, once it has been placed in eye, e.g., in the vitreous
humor, the implant may become shorter to better fit within the
limited, small volume of the eye. The needles used for injection of
the implants of the present invention as disclosed herein, such as
the 25- or 27-gauge needles in certain embodiments, are small in
diameter (and e.g. may have an inner diameter of about 0.4 mm). As
the implant also may become softer upon hydration, injuries of any
ocular tissue can be prevented or minimized even when the implant
comes into contact with such tissue. In certain embodiments, the
dimensional change is enabled at least in part by the "shape
memory" effect introduced into the implant by means of stretching
the implant in the longitudinal direction during its manufacture
(as also disclosed below in the section "Method of manufacture").
In certain embodiments, the stretching may either be performed in
the dry or in the wet state, i.e., after drying the hydrogel
implant, or before drying. It is noted that if no stretching is
performed, and the hydrogel implant is only dried and cut into a
desired length, the implant may increase in both diameter and
length upon hydration. If this is not desired, the hydrogel fiber
may be dry or wet stretched.
[0206] In pre-formed dried hydrogels, a degree of molecular
orientation may be imparted by dry-stretching the material then
allowing it to solidify, locking in the molecular orientation. This
can be accomplished in certain embodiments by drawing the material
(optionally while heating the material to a temperature above the
melting point of the crystallizable regions of the material), then
allowing the crystallizable regions to crystallize. Alternatively,
in certain embodiments the glass transition temperature of the
dried hydrogel can be used to lock in the molecular orientation for
polymers such as PVA that have a suitable glass transition
temperature. Still another alternative is to stretch the gel prior
to complete drying (also referred to as "wet stretching") and then
drying the material while under tension. The molecular orientation
provides one mechanism for anisotropic swelling upon introduction
into a hydrating medium such as the vitreous. Upon hydration the
implant of certain embodiments will swell only in the radial
dimension, while the length will either decrease or be essentially
maintained. The term "anisotropic swelling" means swelling
preferentially in one direction as opposed to another, as in a
cylinder that swells predominantly in diameter, but does not
appreciably expand (or does even contract) in the longitudinal
dimension.
[0207] The degree of dimensional change upon hydration may depend
inter alia on the stretch factor. As an example, stretching at e.g.
a stretch factor of about 1.3 (e.g. by means of wet stretching) may
have a less pronounced effect or may not change the length during
hydration to a large extent. In contrast, stretching at e.g. a
stretch factor of about 1.8 (e.g. by means of wet stretching) may
result in a markedly shorter length during hydration. Stretching at
e.g. a stretch factor of 4 (e.g. by means of dry stretching) could
result in a much shorter length upon hydration (such as, for
example, a reduction in length from 15 to 8 mm). One skilled in the
art will appreciate that other factors besides stretching can also
affect swelling behavior.
[0208] Among other factors influencing the possibility to stretch
the hydrogel and to elicit dimensional change of the implant upon
hydration is the composition of the polymer network. In the case
PEG precursors are used, those with a lower number of arms (such as
4-armed PEG precursors) contribute in providing a higher
flexibility in the hydrogel than those with a higher number of arms
(such as 8-armed PEG precursors). If a hydrogel contains more of
the less flexible components (e.g. a higher amount of PEG
precursors containing a larger number of arms, such as the 8-armed
PEG units), the hydrogel may be firmer and less easy to stretch
without fracturing. On the other hand, a hydrogel containing more
flexible components (such as PEG precursors containing a lower
number of arms, such as 4-armed PEG units) may be easier to stretch
and softer, but also swells more upon hydration. Thus, the behavior
and properties of the implant once it has been placed into the eye
(i.e., once the hydrogel becomes (re-) hydrated) can be tailored by
means of varying structural features as well as by modifying the
processing of the implant after it has been initially formed.
[0209] Exemplary dimensions of implants used in the Examples herein
below are provided inter alia in Tables 6, 21.1 and 21.2 of the
Examples section. Specific implants containing about 200 .mu.g and
about 600 .mu.g axitinib are disclosed in Tables 21.1 and 21.2.
Implants containing about 200 .mu.g or about 600 .mu.g axitinib may
however also have dimensions (i.e., lengths and/or diameters)
differing from the dimensions disclosed in these Tables. The dried
implant dimensions inter alia depend on the amount of TKI
incorporated as well as the ratio of TKI to polymer units and can
also be controlled by the diameter and shape of the mold or tubing
in which the hydrogel is allowed to gel. Furthermore, the diameter
of the implant is further determined inter alia by (wet or dry)
stretching of the hydrogel strand once formed. The dried strand
(after stretching) is cut into segments of the desired length to
form the implant; the length can thus be chosen as desired.
[0210] In the following, embodiments of implants with specific
dimensions are disclosed. Whenever the dimensional ranges or values
disclosed herein relate to the length and the diameter of an
implant, the implant is cylindrical or essentially cylindrical.
However, all values and ranges disclosed herein for lengths and
diameters of cylindrical implants may equally be used for lengths
and widths, respectively, of non-cylindrical implants as also
disclosed herein.
[0211] In certain embodiments, an implant of the present invention
may have in its dry state a length of less than about 17 mm. In
specific embodiments, the length of an implant in its dry states
may be less than about 15 mm, or less than or equal to about 12 mm,
or less than or equal to about 10 mm, or less than or equal to
about 8.5 mm. In specific embodiments, an implant of the present
invention may have in its dry state a length of about 12 to about
17 mm, or may have in its dry state a length of about 6 mm to about
10 mm or specifically of about 6 mm to about 9 mm.
[0212] In certain embodiments, an implant of the present invention
may have in its dry state a diameter of about 0.1 mm to about 0.5
mm. In certain other embodiments, an implant in its dry state may
have a diameter of about 0.2 mm to about 0.5 mm. In specific
embodiments, an implant in its dry state may have a diameter of
about 0.2 mm to about 0.4 mm, or of about 0.3 mm to about 0.4 mm.
In specific embodiments, an implant of the present invention may
have a diameter in the dry state of about 0.2 mm to about 0.3 mm,
or of about 0.3 mm to about 0.4 mm.
[0213] In particular embodiments, an implant in its dry state may
have a legth of about 6 mm to about 10 mm and a diameter of about
0.2 to about 0.4 mm.
[0214] In certain embodiments, an implant of the present invention
may have in its wet/hydrated state a length of about 6 mm to about
12 mm. In certain other embodiments, an implant of the present
invention may have in its wet/hydrated state a length of equal to
or less than about 10 mm, or of about 6 mm to about 10 mm. In
specific embodiments, an implant of the present invention in its
wet/hydrated state may have a length of about 6 mm to about 8
mm.
[0215] In certain embodiments, an implant of the present invention
may have in its wet/hydrated state a diameter of equal to or less
than about 0.8 mm, or of about 0.5 mm to about 0.8 mm, or of about
0.65 mm to about 0.8 mm. In specific embodiments, an implant of the
present invention may have a diameter in its wet/hydrated state of
about 0.7 mm to about 0.8 mm.
[0216] In particular embodiments, an implant in its wet/hydrated
state may have a legth of equal to or less than about 10 mm and a
diameter of equal to or less than about 0.8 mm.
[0217] In embodiments of the present invention, the diameter of an
implant in its dry state must be such that the implant can be
loaded into a thin-diameter needle as disclosed herein, such as a
25-gauge or 27-gauge needle. Specifically, in one embodiment an
implant containing from about 480 .mu.g to about 750 .mu.g axitinib
may have a diameter such that it can be loaded into a 25-gauge
needle, or that it can be loaded into a 27-gauge needle without
afflicting any damage to the implant while loading, and such that
the implant remains stably in the needle during further handling
(including packaging, sterilization, shipping etc.).
[0218] Whenever herein a length or a diameter of an implant of the
invention in the wet/hydrated state is disclosed (in mm), this
disclosure refers to the implant's length or the diameter,
respectively, determined after 24 hours at 37.degree. C. at pH 7.2.
It is understood that in this context a pH of 7.2 comprises a pH
range of about 7.2 to about 7.4.
[0219] The dimensions of an implant may further change (e.g. the
length may increase slightly again) over the course of time (i.e.,
after 24 hours) when the implant remains in these conditions.
However, whenever hydrated dimensions of an implant are reported
herein, these are measured after 24 hours at a pH of 7.2 at
37.degree. C. in PBS as disclosed above.
[0220] In case several measurements of the length or diameter of
one implant are conducted, or several datapoints are collected
during the measurement, the average (i.e., mean) value is reported
as defined herein. The length and diameter of an implant according
to the invention may be measured e.g. by means of microscopy, or by
means of an (optionally automated) camera system as described in
Example 6.1.
[0221] In certain embodiments, an implant of the present invention
may have a ratio of the diameter in the hydrated state to the
diameter in the dry state of less than about 5 mm, or less than
about 4 mm, or less than about 3.25 mm, or less than about 2.5 mm,
or less than about 2.25 mm, or less than about 2.10 mm.
[0222] In certain same or other embodiments, an implant of the
present invention may have a ratio of the length in the dry state
to the length in the hydrated state of greater than about 0.7, or
greater than about 0.8, or greater than about 0.9, or greater than
about 1.0. In certain specific embodiments, the ratio of the length
of an implant in the dry state to the length of the implant in the
hydrated state may be greater than about 1.5, or even greater than
about 2.0. This ratio of length in the dry state to length in the
hydrated state may apply in addition to, or independently of, the
ratio of the diameter in the hydrated state to the diameter in the
dry state disclosed above.
[0223] A small diameter in the dry state may be advantageous as the
implant may fit into a small diameter needle for injection as
disclosed herein, such as a 25-gauge or a 27-gauge needle. Also,
only moderate swelling upon hydration may be advantageous for the
implant to not occupy too much space in the vitreous humor. A
relatively shorter length of the implant may be advantageous in
reducing the potential likelihood for contact with the retina.
[0224] In one embodiment, an implant of the present invention
contains from about 160 .mu.g to about 250 .mu.g, or from about 180
.mu.g to about 220 .mu.g, or about 200 .mu.g axitinib, is in the
form of a fiber (or cylinder) and has a length of about 14.5 mm to
about 17 mm, or of about 15 mm to about 16.5 mm and a diameter of
about 0.20 mm to about 0.30 mm in the dried state. Such an implant
may decrease in length and increase in diameter upon hydration in
vivo in the eye, such as in the vitreous humor, or in vitro
(wherein hydration in vitro is measured in phosphate-buffered
saline at a pH of 7.2 at 37.degree. C. after 24 hours) to a length
of about 6.5 mm to about 8 mm or of about 7 mm to about 8.5 mm, and
a diameter of about 0.65 mm to about 0.8 mm, or of about 0.70 to
about 0.80 mm. In one embodiment, this dimensional change may be
achieved by dry stretching as disclosed herein at a stretch factor
of about 2 to about 5, or a stretch factor of about 3 to about
4.5.
[0225] In another embodiment, an implant of the present invention
contains from about 480 .mu.g to about 750 .mu.g, or from about 540
.mu.g to about 660 .mu.g, or about 600 .mu.g of axitinib, is in the
form of a fiber (cylinder) and in its dried state may have a length
of in the range of from about 6 mm or about 7 mm to about 12 mm and
a diameter of about 0.25 mm to about 0.50 mm, or a length of about
7 mm to about 10 mm, or of about 8 mm to about 11 mm, and a
diameter of about 0.3 mm to about 0.4 mm. In specific embodiments,
an implant of the present invention that contains from about 480
.mu.g to about 750 .mu.g, or from about 540 .mu.g to about 660
.mu.g, or about 600 .mu.g of axitinib, is in the form of a fiber
(cylinder) and in its dried state may have a length of from about 7
mm to about 10 mm, such as from about 7 mm to about 9 mm, and a
diameter of from about 0.3 mm to about 0.4 mm, such as from about
0.35 mm to about 0.39 mm.
[0226] Such an implant may increase in diameter upon hydration in
vivo in the eye, such as in the vitreous humor, or in vitro
(wherein hydration in vitro is measured in phosphate-buffered
saline at a pH of 7.2 at 37.degree. C. after 24 hours) while its
length may be essentially maintained or may be reduced, or only
slightly increased to a length of e.g. in the range of from about 6
mm or about 9 mm to about 12 mm and a diameter of about 0.5 mm to
about 0.8 mm, or a length of about 9.5 mm to about 11.5 mm and a
diameter of from about 0.65 mm to about 0.75 mm or about 0.8 mm in
its hydrated state. In specific embodiments, an implant of the
present invention that contains from about 480 .mu.g to about 750
.mu.g, or from about 540 .mu.g to about 660 .mu.g, or about 600
.mu.g of axitinib and is in the form of a fiber (cylinder) in its
hydrated state (i.e., at a pH of 7.2 at 37.degree. C. after 24
hours as explained above) may have a length of from about 6 mm to
about 10.5 mm, such as from about 6.5 mm to about 8.5 mm, and a
diameter from about 0.7 mm to about 0.8 mm.
[0227] In one embodiment, the length of an implant of the present
invention that contains from about 480 .mu.g to about 750 .mu.g, or
from about 540 .mu.g to about 660 .mu.g, or about 600 .mu.g of
axitinib in the dried state is no longer than 10 mm, and in the
hydrated state (as measured in phosphate-buffered saline at a pH of
7.2 at 37.degree. C. after 24 hours) is also no longer or not
substantially longer than about 10 mm, or no longer than about 9
mm, or no longer than about 8 mm.
[0228] In one or more embodiment(s), the above-described
dimensional change can be achieved by wet stretching at a stretch
factor of about 0.5 to about 5, or a stretch factor of about 1 to
about 4, or a stretch factor of about 1.3 to about 3.5, or a
stretch factor of about 1.7 to about 3, or a stretch factor of
about 2 to about 2.5. In other embodiments the implant of the
present invention containing from about 480 .mu.g to about 750
.mu.g, or from about 540 .mu.g to about 660 .mu.g, or about 600
.mu.g of axitinib may be longer than about 12 mm in the dry state,
but may end up being shorter than about 10 mm or about 9 mm in the
hydrated state.
[0229] In certain embodiments, the stretching thus creates a shape
memory, meaning that the implant upon hydration when administered
into the eye, e.g., into the vitreous cavity, will shrink in length
and widen in diameter until it approaches (more or less) its
equilibrium dimensions, which are determined by the original molded
dimensions and compositional variables. While the narrow dry
dimensions facilitate administration of the product through a small
gauge needle, the widened diameter and shortened length after
administration yield a shorter implant (such as about 9 to 10 mm
long, or at least not much longer than that) in the posterior
chamber of the eye relative to the eye diameter minimizing
potential contact with surrounding eye tissues. Thus, in one aspect
the present invention also relates to a method of imparting shape
memory to a hydrogel fiber comprising an active agent such as a
TKI, e.g. axitinib, dispersed in the hydrogel by stretching the
hydrogel fiber in the longitudinal direction. In another aspect the
present invention relates to a method of manufacturing an ocular
implant comprising a hydrogel comprising an active agent, such as a
TKI, e.g. axitinib, dispersed therein, wherein the implant changes
its dimensions upon administration to the eye, the method
comprising preparing a fiber of the hydrogel and stretching the
fiber in the longitudinal direction.
In Vitro Release:
[0230] The in vitro-release of TKI from the implants of the
invention can be determined by various methods disclosed in detail
in Example 2:
[0231] Briefly, one method to determine the in vitro release of the
TKI from the implant is under non-sink simulated physiological
conditions in PBS (phosphate-buffered saline, pH 7.2) at 37.degree.
C., with daily replacement of PBS in a volume comparable to the
vitreous volume in the human eye. Results for exemplary implants
are shown in FIG. 4A. In the tested implants comprising axitinib in
a PEG hydrogel matrix as described in Example 2 the higher dose
strengths resulted in higher axitinib concentrations in the release
medium.
[0232] Generally, in embodiments of the invention, an implant
according the invention may release on average about 0.1 .mu.g to
about 3 .mu.g, or about 0.25 .mu.g to about 2.5 .mu.g, or about 0.1
.mu.g to about 2 .mu.g, or may release about 0.25 .mu.g to about
1.5 .mu.g per day in vitro in PBS at pH 7.2 and 37.degree. C. for a
period of 30 days.
[0233] In one embodiment, an implant according to the invention
containing about 200 .mu.g axitinib, may release on average in
vitro about 0.01 .mu.g to about 0.15 .mu.g of axitinib per day in
phosphate-buffered saline at pH 7.2 and 37.degree. C. for a period
of 30 days.
[0234] In one embodiment, an implant according to the invention
containing about 600 .mu.g axitinib may release on average in vitro
about 0.3 .mu.g to about 0.5 .mu.g of axitinib per day in
phosphate-buffered saline at pH 7.2 and 37.degree. C. for a period
of 30 days.
[0235] In an accelerated in vitro test, also described in detail in
Example 2, the release of the TKI from the implant can be
determined in a 25:75 ethanol/water mixture (v/v) at 37.degree. C.
This accelerated in vitro test can be completed in about 2 weeks.
FIG. 14B shows the accelerated in vitro release data for an implant
according to the invention containing about 200 .mu.g axitinib, and
FIG. 4B the accelerated in vitro release data for an implant
according to the invention containing about 556 .mu.g axitinib.
[0236] In one embodiment, an implant according to the invention
containing about 200 .mu.g axitinib releases in vitro about 35% to
about 45% of the axitinib in 3 days, about 65% to about 75% of the
axitinib in 7 days, and about 90% to about 100% of the axitinib in
12 to 13 days in a 25:75 ethanol/water mixture (v/v) at 37.degree.
C.
[0237] In one embodiment, an implant according to the invention
containing about 600 .mu.g axitinib releases in vitro about 40% to
about 60% of the axitinib in 2 days, about 65% to about 85% of the
axitinib in 4 days, and about 75% to about 90% of the axitinib in 6
days in a 25:75 ethanol/water mixture (v/v) at 37.degree. C. An
implant according to the invention containing about 600 .mu.g
axitinib may also release in vitro about 45% to about 55% of the
axitinib in 2 days, about 70% to about 80% of the axitinib in 4
days, and about 80% to about 90% of the axitinib in 6 days in a
25:75 ethanol/water mixture (v/v) at 37.degree. C.
[0238] Finally, the release of TKI from implants of the present
invention can also be determined under real-time sink simulated
physiological conditions, as also described in detail in Example 2.
For this real-time test, release of the TKI is determined in PBS
(pH 7.2)/0.01% NaF at 37.degree. C. with an octanol top layer on
the PBS. This is one method to qualitatively simulate release of
the TKI from the implant into the vitreous humor and from there
resorption of the TKI into ocular tissue. An exemplary real-time
release profile for an implant according to the present invention
containing about 200 .mu.g axitinib is shown in FIG. 14A.
[0239] In one embodiment, an implant according to the invention
containing about 200 .mu.g axitinib releases in vitro about 25% to
about 35% of the axitinib in 2 months, about 47% to about 57% of
the axitinib in 3 months, about 70% to about 80% of the axitinib in
5 months, and about 90% to about 100% of the axitinib in 7 months
in phosphate buffered saline at a pH of 7.2, at 37.degree. C. and
with an octanol top layer.
[0240] The in vitro release tests, especially the accelerated in
vitro release test described herein, may be used inter alia to
compare different implants (e.g. of different production batches,
of different composition, and of different dosage strength etc.)
with each other, for example for the purpose of quality control or
other qualitative assessments.
In Vivo Release and Persistence:
[0241] In an embodiment of the present invention, when the dried
implant of the present invention is administered to the eye, such
as the vitreous humor, it becomes hydrated and changes its
dimensions as disclosed above, and is then over time biodegraded
until it has been fully resorbed. When the implant is biodegraded,
such as through ester hydrolysis, it gradually may swell and
soften, then become smaller, softer and more liquid until it is
fully dissolved and no longer visible. As recognized by the
inventors from the animal studies presented in the Examples section
herein below, an implant according to the invention may persist
about 2 to about 6 months, or about 5 to about 6 months in rabbit
eyes (see FIGS. 7A, 9 and 10). After full degradation of the
implant, undissolved axitinib particles may remain at the former
site of the implant and have been observed to agglomerate, i.e.,
merge into a monolithic structure. These remaining undissolved
axitinib particles may continue to dissolve slowly at a rate
sufficient to provide therapeutically effective axitinib levels. If
in certain embodiments two or more implants are administered to
achieve a desired total dose, they are equally biodegraded over
time, and the remaining axitinib particles also merge into one
single monolithic structure (see FIG. 9).
[0242] In the human eye, such as in the vitreous humor, the implant
of the invention in certain embodiments biodegrades within about 2
to about 15 months after administration, or within about 4 to about
13 months after administration, or within about 9 to about 12
months after administration, specifically within about 9 to about
10.5 months after administration. This has been demonstrated in the
clinical trials with one or two implant(s), each comprising about
200 .mu.g axitinib. See the Examples section, in particular Example
6 and FIG. 15.
[0243] In one embodiment, the implant after administration to the
vitreous humor releases (as defined herein) the TKI, such as a
therapeutically effective amount of TKI, such as axitinib, over a
period of at least about 3 months, at least about 6 months, at
least about 9 months, at least about 10 months, at least about 11
months, or at least about 12 months, or at least about 13 months or
longer after administration. In particular embodiments, the implant
releases the TKI, such as axitinib, for a period of about 6 to
about 9 months.
[0244] In one embodiment of the invention, the implant provides for
a treatment period of at least about 3 months, at least about 9
months, at least about 10 months, at least about 11 months, at
least about 12 months, or at least about 13 months or longer after
administration of the (i.e., a single) implant into the vitreous
humor of a patient.
[0245] In one embodiment of the invention, TKI, such as axitinib is
released from the implant at an average rate of about 0.1 .mu.g/day
to about 10 .mu.g/day, or about 0.5 .mu.g/day to about 7 .mu.g/day,
or about 0.5 .mu.g/day to about 2 .mu.g/day, or about 1 .mu.g/day
to about 5 .mu.g/day in the vitreous humor, over a time period of
at least 3, or at least 6, or at least 9, or at least 11, or at
least 12, or at least 13 months. In particular embodiments the
release of TKI, such as axitinib, is maintained for about 6 to
about 9 months after administration of the implant.
[0246] Pre-clinical studies in animals as well as clinical studies
in humans, as presented in the Examples section herein, have shown
that the implants of the invention may continuously release
therapeutically effective amounts of TKI over an extended period of
time, until the implants are fully biodegraded. Any remaining
undissolved TKI particles (if present) may essentially remain at
the site of the former implant and may agglomerate to form an
essentially monolithic structure (see FIGS. 7A, 9 and 10) that may
continue to release TKI into the vitreous at levels sufficient to
achieve the therapeutic effect. In certain embodiments, however,
the entire amount of TKI contained in the implant is released from
the implant prior to complete biodegradation of the implant. In
this case, no undissolved TKI particles would remain (and/or
agglomerate) near the site of the former implant or elsewhere in
the eye after complete biodegradation of the implant.
[0247] In one embodiment, the persistence of the hydrogel within an
aqueous environment and in the human eye depends inter alia on the
hydrophobicity of the carbon chain in proximity to the degradable
ester group. In the implants used in the Examples herein, this
carbon chain comprises 7 carbon atoms as it stems from the SAZ
functional group of the 4a20k PEG precursor. This may provide an
extended persistence in the human eye of up to about 9 to about 12
months, or from about 9 to about 10.5 months. In other embodiments,
different precursors than the 4a20kPEG-SAZ and the
8a20kPEG-NH.sub.2 may be used to prepare hydrogel implants that
biodegrade in the human eye and have similar or different
persistence as the implants exemplified in the Examples.
[0248] In certain embodiments, the hydrogel implant softens over
time as it degrades, which may depend inter alia on the structure
of the linker that crosslinks the PEG units in the hydrogel. An
implant as used in the examples of the present application formed
from a 4a20kPEG-SAZ and a 8a20kPEG-NH.sub.2 softens rather slowly
over time.
Mechanism of Release:
[0249] Without wishing to be bound by theory, the mechanism of
release of the TKI from an implant of the invention may be
explained as follows: In embodiments of the invention, release of
the TKI into the eye and into the vitreous humor is dictated by
diffusion and drug clearance. An exemplary TKI according to the
present invention is axitinib. The solubility of axitinib has been
determined to be very low in physiological medium (about 0.4 to
about 0.5 .mu.g/mL in PBS at pH 7.2). According to the present
invention, the TKI, such as axitinib, is confined in a
biodegradable hydrogel having a particular geometry and surface.
The liquid in the posterior chamber of the eye is viscous, has a
slow clearance and a relatively stagnant flow (at least as compared
to the anterior chamber of the eye).
[0250] In certain embodiments, the implant of the present invention
comprises a hydrogel made of a polymer network and a drug dispersed
within the hydrogel. The drug gradually gets dissolved and diffuses
out of the hydrogel into the eye. This may happen first at the
outer region of the hydrogel (i.e., the drug particles that are
located in the outermost region of the hydrogel get dissolved and
diffuse out first, the innermost last) that is in contact with the
liquid environment of the vitreous. Thereby, in certain
embodiments, the outer region of the hydrogel becomes devoid of
drug particles. This region is therefore also called the "clearance
zone", which is limited to dissolved drug only, with a
concentration at or below the solubility of the drug. In certain
embodiments, this low surface concentration may protect tissue
(retinal or other cells) from potential drug toxicity by physically
separating drug particles from the tissue should the implant get in
contact with such tissue. In other embodiments, upon hydration the
"clearance zone" is an outer region that has a concentration of
active agent that is less than the active agent in an inner region
of the hydrated hydrogel.
[0251] In embodiments with clearance zones, because drug has
dissolved and has diffused out of the clearance zone, this area of
the hydrogel develops voids and becomes softer and weaker.
Concurrently with the drug diffusing out of the hydrogel, the
hydrogel may also be slowly degraded by means of, e.g., ester
hydrolysis in the aqueous environment of the eye. This degradation
occurs uniformly throughout the bulk of the hydrogel. At advanced
stages of degradation, distortion and erosion of the hydrogel
begins to occur. As this happens, the hydrogel becomes softer and
more liquid (and thus its shape becomes distorted) until the
hydrogel finally dissolves and is resorbed completely. This process
is schematically shown on FIG. 3 and demonstrated by means of
infrared reflectance (IR) imaging e.g. in FIG. 10.
[0252] As axitinib is a relatively low solubility drug, undissolved
axitinib particles may remain at the former site of the implant
after the implant has already fully degraded in certain
embodiments. Since these remaining undissolved axitinib particles
are no longer fixated and held apart by the hydrogel, they may
agglomerate and form a substantially monolithic structure. This
monolithic axitinib structure may still continue to release
axitinib, at rates sufficient to achieve the therapeutic effect
(specifically, to reduce CSFT).
[0253] In one embodiment, however, the entire amount of axitinib is
released prior to the complete degradation of the hydrogel. As the
hydrogel may hold the axitinib particles in place and prevent them
from agglomeration the release of axitinib from the hydrogel can be
faster as long as the hydrogel has not yet fully degraded. When the
hydrogel has fully degraded, remaining axitinib particles may form
a monolithic structure from which axitinib may slowly be dissolved.
Therefore, complete release of the axitinib prior to full
degradation of the hydrogel is desired in one embodiment of the
invention.
[0254] This whole process makes it possible in certain embodiments
to advantageously maintain the therapeutic effect of the implant of
the present invention over an extended period of time, such as at
least 3 months, or at least 6 months, or at least 9 months, or at
least 11 months, or at least 12 months, or at least 13 months, or
at least 14 months, or even longer, such as up to 15 months. It has
been demonstrated by the present inventors that this is a great
advantage for patients receiving treatment for neovascular
age-related macular degeneration, which treatment previously
involved very frequent intravitreal injections of an anti-VEGF
agent. In contrast, the implants according to the present invention
may need to be injected only at much greater intervals of time,
which is advantageous for the patient for a number of reasons as
already disclosed above in the section "Objects and Summary".
Specific Implant Containing from about 160 .mu.g to about 250 .mu.g
Such as about 200 .mu.g Axitinib:
[0255] In one particular embodiment, the present invention relates
to a sustained release biodegradable ocular implant containing
axitinib in an amount in the range from about 160 .mu.g to about
250 .mu.g, or from about 180 .mu.g to about 220 .mu.g, and
specifically about 200 .mu.g dispersed in a hydrogel, wherein the
hydrogel comprises a polymer network comprising polyethylene glycol
units, and wherein the implant is in a dried state. In this
embodiment the polymer network contains polyethylene glycol units
comprising multi-arm polyethylene glycol units, such as 4-arm
and/or 8-arm polyethylene glycol units having an average molecular
weight in the range of from about 10,000 Daltons to about 60,000
Daltons. In this embodiment, the polymer network of this implant is
formed by reacting 4a20kPEG-SAZ with 8a20kPEG-NH.sub.2, at a weight
ratio of about 2:1. In this embodiment the hydrogel when formed and
before being dried (i.e., the wet composition) contains about 6.5%
to about 7.5% polyethylene glycol, representing the polyethylene
glycol weight divided by the fluid weight.times.100. Also, in this
embodiment the implant in a dried state contains from about 45% to
about 55% by weight axitinib and from about 37% to about 47% by
weight polyethylene glycol units, or from about 47% to about 52% by
weight axitinib and from about 40% to about 45% by weight
polyethylene glycol units, such as about 49% to about 50% by weight
axitinib and about 42% by weight PEG units, or about 47% by weight
axitinib and about 44% by weight PEG units (dry composition), the
balance being sodium phosphate. The implant furthermore in its
dried state may contain not more than about 1% by weight water, or
not more than about 0.25% by weight water.
[0256] In this embodiment, the implant containing axitinib in an
amount in the range from about 160 .mu.g to about 250 .mu.g, or
from about 180 .mu.g to about 220 .mu.g, and specifically about 200
.mu.g releases in vitro about 0.01 .mu.g to about 0.15 .mu.g of
axitinib per day in phosphate-buffered saline at 37.degree. C. for
a period of 30 days. Furthermore, in this embodiment the implant
releases in vitro about 35% to about 45% of the axitinib in 3 days,
about 65% to about 75% of the axitinib in 7 days, and about 90% to
about 100% of the axitinib in 12 to 13 days in a 25:75
ethanol/water (v/v) mixture at 37.degree. C. In this embodiment the
implant may also release in vitro about 25% to about 35% of the
axitinib in 2 months, about 47% to about 57% of the axitinib in 3
months, about 70% to about 80 of the axitinib in 5 months, and
about 90% to about 100% of the axitinib in 7 months in phosphate
buffered saline at a pH of 7.2, at 37.degree. C. and with an
octanol top layer.
[0257] In this embodiment, the implant containing about 200 .mu.g
axitinib may be in the form of a fiber (or cylinder) and may have a
length of less than about 20 mm, or less than about 17 mm, or of
about 15 mm to about 16.5 mm and a diameter of about 0.20 mm to
about 0.30 mm in its dried state and may decrease in length and
increases in diameter upon hydration in vivo in the vitreous humor
or in vitro (wherein hydration in vitro is measured in
phosphate-buffered saline at a pH of 7.2 at 37.degree. C. after 24
hours) to a length of about 6.5 mm to about 8 mm and a diameter of
about 0.70 mm to about 0.80 mm in the hydrated state. This
dimensional change upon hydration may be achieved by imparting
shape memory to the implant by dry stretching the implant in the
longitudinal direction as explained in more detail elsewhere
herein, by a stretch factor of about 2 to about 5, or a stretch
factor of about 3 to about 4.5. In other embodiments, the implant
may be non-cyclindrical.
[0258] In this embodiment, the implant containing about 200 .mu.g
axitinib may have a ratio of the diameter in the hydrated state to
the diameter in the dry state of less than about 3.25 mm, and/or a
ratio of the length in the dry state to the length in the hydrated
state of greater than about 1.5.
[0259] The total weight of an implant as disclosed in this
embodiment in its dry state may be from about 0.3 mg to about 0.6
mg, such as from about 0.4 mg to about 0.5 mg. Such an implant in
the dry state may contain about 10 .mu.g to about 15 .mu.g of
axitinib per 1 mm final length, and may contain from about 200
.mu.g to about 300 .mu.g axitinib per mm.sup.3.
[0260] In this embodiment, prior to administration, the implant
containing an axitinib dose of about 200 .mu.g is loaded into a
25-gauge needle or a 27-gauge needle (or an even smaller gauge
needle, such as a 30-gauge needle) for injection into the vitreous
humor.
[0261] To summarize and exemplify, the individual characteristics
of an implant of the invention disclosed with respect to the
embodiment described in this section containing a dose of about 200
.mu.g (including the implant that is used in the clinical study
presented in Example 6) are provided in Table 21.1 in the Examples
section, which is also reproduced here:
TABLE-US-00001 Implant type Implant #1 Formulation Axitinib 49.4%
(% dry Dose (200 .mu.g) basis w/w) PEG Hydrogel 42.0% 4a20K PEG-SAZ
28% 8a20K PEG-NH2 14% Sodium phosphate 8.6% Formulation Axitinib
7.5% (% wet PEG Hydrogel 6.9% basis w/w) 4a20K PEG-SAZ 4.6% 8a20K
PEG-NH2 2.3% Sodium phosphate 1.5% WFI 84.1% Axitinib per final dry
12.1 .mu.g/mm length Approximate Implant 423 Mass (dose .mu.g/API
%) Configuration Stretching Method Dry (Stretch Factor) (4.5)
Needle Size 27G TW 1.25'' (0.27 mm ID) Injector/Syringe Implant
Injector Packaging Foil Pouches Sterilization Type Gamma Site
Storage Refrigerated Dimensions Dried Diameter 0.24 .+-. 0.013 mm
Length 16.5 .+-. 0.26 mm Volume 0.75 .+-. 0.08 mm.sup.3 Implant
Mass 0.45 mg Axitinib per volume 266.7 (.mu.g/mm.sup.3) Hydrated
Diameter 0.75 mm Length 7.5 mm Ratio of diameter 3.13 (hydrated) to
diameter (dry) Ratio of length (dry) 2.20 to length (hydrated)
[0262] The sustained release biodegradable ocular implant of claim
1, wherein the implant is an intravitreal implant and comprises
from about 180 .mu.g to about 220 .mu.g axitinib, is cylindrical
and has in its dry state a length of less than about 17 mm and a
diameter of about 0.2 mm to about 0.3 mm, and in its hydrated state
(after 24 hours in phosphate-buffered saline at a pH of 7.2 at
37.degree. C.) has a length of from about 6.5 mm to about 8 mm and
a diameter of from about 0.7 mm to about 0.8 mm, and wherein the
hydrogel comprises crosslinked 4a20k and 8a20k PEG units, wherein
the crosslinks between the PEG units include a group represented by
the following formula
##STR00005##
wherein m is 6.
[0263] Alternatively, an implant of this particular embodiment may
also be non-cyclindrical as disclosed herein.
Specific Implant Containing about 480 .mu.g to about 750 .mu.g Such
as about 600 .mu.g Axitinib:
[0264] In another particular embodiment, the present invention
relates to a sustained release biodegradable ocular implant
containing axitinib in an amount in the range from about 480 .mu.g
to about 750 .mu.g dispersed in a hydrogel, wherein the hydrogel
comprises a polymer network that comprises crosslinked polyethylene
glycol units. The amount of axitinib in said implant may also be in
the range from about 540 .mu.g to about 660 .mu.g, or may
specifically be about 600 .mu.g.
[0265] In this implant, the polyethylene glycol units comprise
multi-arm polyethylene glycol units, such as 4-arm and/or 8-arm
polyethylene glycol units having an average molecular weight in the
range of from about 10,000 Daltons to about 60,000 Daltons. In this
embodiment, the polymer network of the implant comprises 4a20kPEG
and 8a20kPEG units and is formed by reacting 4a20kPEG-SAZ with
8a20kPEG-NH.sub.2, in a weight ratio of about 2:1.
[0266] In this embodiment, the implant in a dried state may contain
from about 45% to about 55% by weight axitinib and from about 37%
to about 47% by weight polyethylene glycol units, or may contain
from about 60% to about 75% by weight axitinib and from about 21%
to about 31% polyethylene glycol units, such as from about 63% to
about 72% by weight axitinib and from about 23% to about 27%
polyethylene glycol units (dry composition), the balance being
sodium phosphate. In certain specific embodiments the implant may
contain about 68% to about 69% axitinib and about 26% polyethylene
glycol units (dry composition), the balance being sodium phosphate.
The implant may contain not more than about 1% by weight water, or
not more than about 0.25% by weight water.
[0267] In this embodiment, this implant containing axitinib in an
amount in the range from about 480 .mu.g to about 750 .mu.g, or
from about 540 .mu.g to about 660 .mu.g, or specifically about 600
.mu.g releases in vitro about 0.3 .mu.g to about 0.5 .mu.g of
axitinib per day in phosphate-buffered saline at 37.degree. C. for
a period of 30 days. Furthermore, this implant releases in vitro
about 40% to about 60% of the axitinib in 2 days, about 65% to
about 85% of the axitinib in 4 days, and about 75% to about 90% of
the axitinib in 6 days in a 25:75 (v/v) ethanol/water mixture at
37.degree. C. In this embodiment, this implant may also release in
vitro about 45% to about 55% of the axitinib in 2 days, about 70%
to about 80% of the axitinib in 4 days, and about 80% to about 90%
of the axitinib in 6 days in a 25:75 ethanol/water (v/v) mixture at
37.degree. C.
[0268] In this embodiment, the implant containing about 600 .mu.g
axitinib may be in the form of a fiber (or cylinder) and may have
in its dried state a length of less than about 20 mm, or less than
about 17 mm, or less than about 15 mm, or less than or equal to
about 12 mm, such as about 7 mm to about 12 mm and a diameter of
about 0.25 mm to about 0.50 mm, or a length of from about 7 mm or
about 8 mm to about 11 mm and a diameter of about 0.3 mm to about
0.4 mm, and may increase in diameter upon hydration in vivo in the
vitreous humor or in vitro (wherein hydration in vitro is measured
in phosphate-buffered saline at a pH of 7.2 at 37.degree. C. after
24 hours). In specific embodiments, an implant containing about 600
.mu.g of axitinib in its dried state may have a length of less than
or equal to about 10 mm, or less than or equal to about 8.5 mm, or
from about 7 mm to about 9 mm, or from about 7 mm to about 8.5 mm
and a diameter of from about 0.3 mm to about 0.4 mm, such as from
about 0.35 mm to about 0.39 mm.
[0269] The dimensions of this implant after hydration in vivo or in
vitro (wherein in vitro hydration is measured in phosphate-buffered
saline at a pH of 7.2 at 37.degree. C. after 24 hours) may be a
length of less than or equal to about 10 mm, such as of from about
6 mm or about 9 mm to about 12 mm and a diameter of about 0.5 mm to
about 0.8 mm, or a length of about 9.5 mm to about 11.5 mm, or a
length of not more than about 10 mm or not more than about 9 mm,
and a diameter of from about 0.65 mm to about 0.75 mm or to about
0.80 mm. In specific embodiments, an implant containing about 600
.mu.g of axitinib in its hydrated state (wherein hydration in vitro
is measured in phosphate-buffered saline at a pH of 7.2 at
37.degree. C. after 24 hours) may have a length of from about 6 mm
to about 10.5 mm, such as from about 6.5 mm to about 8.5 mm, and a
diameter of from about 0.7 mm to about 0.8 mm. In particular
embodiments, a length of about 10 mm or less, such as about 9 mm or
less when hydrated in the vitreous humor of the eye is an
acceptable length given the limited volume of the eye.
[0270] This dimensional change upon hydration may be achieved by
wet stretching in the longitudinal direction prior to drying as
disclosed in more detail below by a stretch factor of about 0.5 to
about 5, or a stretch factor of about 1 to about 4, or a stretch
factor of about 1.3 to about 3.5, or a stretch factor of about 1.7
to about 3, or a stretch factor of about 2 to about 2.5.
[0271] In this embodiment, the implant containing about 600 .mu.g
axitinib may have a ratio of the diameter in the hydrated state to
the diameter in the dry state of less than about 2.25 mm and/or a
ratio of the length in the dry state to the length in the hydrated
state of greater than 0.75.
[0272] The total weight of an implant as disclosed herein
containing about 600 .mu.g axitinib may in the dry state be from
about 0.8 mg to about 1.1 mg, such as from about 0.9 mg to about
1.0 mg. Such an implant in the dry state may contain about 70 .mu.g
to about 85 .mu.g of axitinib per 1 mm final length, and may
contain from about 500 .mu.g to about 800 .mu.g axitinib per
mm.sup.3.
[0273] In this embodiment, the preferred shape of the implant is
cylindrical or essentially cylindrical (and may also be referred to
as a fiber). In other embodiments, the implant may be
non-cylindrical. Prior to administration, this implant containing
an axitinib dose of about 600 .mu.g is loaded into a 25-gauge (or a
smaller gauge, such as a 27-gauge) needle for injection into the
eye, e.g., the vitreous humor.
[0274] To summarize, the individual characteristics of implants of
the invention disclosed with respect to the embodiment described in
this section containing a dose of about 600 .mu.g axitinib are
provided in Table 21.2 in the Examples section, which is also
reproduced here:
TABLE-US-00002 Implant type Implant #2 Implant #3 Implant #4
Formulation Axitinib 49.8% 68.6% 68.6% (% dry Dose (600 .mu.g) (600
.mu.g) (600 .mu.g) basis w/w) PEG Hydrogel 42.0% 26.0% 26.0% 4a20K
PEG-SAZ 28% 17.4% 17.4% 8a20K PEG-NH2 14% 8.7% 8.7% Sodium
phosphate 8.2% 5.4% 5.4% Formulation Axitinib 12.0% 16.5% 16.5% (%
wet PEG Hydrogel 6.3% 6.3% 6.3% basis w/w) 4a20K PEG-SAZ 4.2% 4.2%
4.2% 8a20K PEG-NH2 2.1% 2.1% 2.1% Sodium phosphate 1.3% 1.3% 1.3%
WFI 80.4% 75.9% 75.9% Axitinib per final dry 71.4 .mu.g/mm 71.4
.mu.g/mm 81.1 .mu.g/mm length Approximate Implant 1205 875 875 Mass
(dose ug/API %) Configuration Stretching Method Wet Wet Wet
(Stretch Factor) (2.1) (2.1) (2.1) Needle Size 25G UTW 1'' 25G UTW
1'' 25G UTW 0.5'' (0.4 mm ID) (0.4 mm ID) (0.4 mm ID)
Injector/Syringe Implant Injector Implant Injector Implant Injector
Packaging Foil Pouches Foil Pouches Foil Pouches Sterilization Type
Gamma Gamma Gamma Site Storage Refrigerated Refrigerated
Refrigerated Dimensions Dried Diameter 0.36 mm 0.37 .+-. 0.014 mm
0.37 .+-. 0.008 mm Length 8.4 mm 8.4 .+-. 0.04 mm 7.4 .+-. 0.03 mm
Volume 0.86 mm.sup.3 0.90 .+-. 0.07 mm.sup.3 0.81 .+-. 0.05
mm.sup.3 Implant Mass 1.20 mg 0.95 .+-. 0.04 mg 0.95 .+-. 0.01 mg
Axitinib per volume 697.7 666.7 740.7 (.mu.g/mm.sup.3) Hydrated
Diameter 0.7 mm 0.68 mm 0.77 mm Length 10 mm 8.23 mm 6.8 mm Ratio
of diameter 1.94 1.84 2.08 (hydrated) to diameter (dry) Ratio of
length (dry) 0.84 1.02 1.09 to length (hydrated)
[0275] In a particular embodiment, the sustained release
biodegradable ocular implant of the present invention is an
intravitreal implant and comprises from about 540 .mu.g to about
660 .mu.g axitinib, is cylindrical and has in its dry state a
length of less than or equal to 10 mm and a diameter of about 0.3
mm to about 0.4 mm, and in its hydrated state (after 24 hours in
phosphate-buffered saline at a pH of 7.2 at 37.degree. C.) has a
length of from about 6 mm to about 10.5 mm and a diameter of from
about 0.6 mm to about 0.8 mm, and wherein the hydrogel comprises
crosslinked 4a20k and 8a20k PEG units, wherein the crosslinks
between the PEG units include a group represented by the following
formula
##STR00006##
wherein m is 6.
[0276] Alternatively, an implant of this particular embodiment may
also be non-cyclindrical as disclosed herein.
II. Manufacture of the Implant
Manufacturing Process:
[0277] In certain embodiments, the present invention also relates
to a method of manufacturing a sustained release biodegradable
ocular implant as disclosed herein. Generally, the method comprises
the steps of forming a hydrogel comprising a polymer network and
TKI particles dispersed within the hydrogel, shaping the hydrogel
and drying the hydrogel. In certain embodiments the method
comprises the steps of forming a hydrogel comprising a polymer
network from reactive group-containing precursors (e.g., comprising
PEG units) and TKI particles dispersed in the hydrogel, shaping the
hydrogel and drying the hydrogel, more specifically the polymer
network is formed by mixing and reacting an electrophilic
group-containing multi-arm PEG precursor with a nucleophilic
group-containing multi-arm PEG precursor or another nucleophilic
group-containing crosslinking agent (precursors and crosslinking
agent as disclosed herein in the sections "The polymer network" and
"PEG hydrogels") in a buffered solution in the presence of TKI
particles and allowing the mixture to gel to form the hydrogel. In
embodiments of the invention, the hydrogel is shaped into a
hydrogel strand as disclosed herein, by casting the mixture into a
tubing prior to complete gelling of the hydrogel. In certain
embodiments, the hydrogel strand is stretched in the longitudinal
direction prior to or after drying as further disclosed herein.
[0278] In certain embodiments, the TKI in the method of
manufacturing according to the invention in all its aspects is
axitinib. In one embodiment the TKI, such as axitinib, may be used
in micronized form for preparing the implant as disclosed herein,
and may have a particle diameter as also disclosed herein in the
section "The active principle". In certain specific embodiments,
the axitinib may have a d90 of less than about 30 .mu.m, or less
than about 10 .mu.m. Using micronized TKI, specifically micronized
axitinib, may have the effect of reducing the tendency of the TKI,
specifically axitinib, particles to agglomerate during casting of
the hydrogel strands, as demonstrated in FIG. 24. In another
embodiment, the TKI, such as axitinib, may be used in
non-micronized form for preparing the implant.
[0279] The precursors for forming the hydrogel of certain
embodiments have been disclosed in detail above in the section
relating to the implant itself. In case PEG precursors are used to
prepare a crosslinked PEG network, the method of manufacturing the
implant in certain embodiments may comprise mixing and reacting an
electrophilic group-containing polymer precursor, such as an
electrophilic group-containing multi-arm polyethylene glycol, such
as 4a20kPEG-SAZ, with a nucleophilic group-containing polymer
precursor or other cross-linking agent, such as a nucleophilic
group-containing multi-arm polyethylene glycol, such as
8a20kPEG-NH.sub.2, in a buffered solution in the presence of the
tyrosine kinase inhibitor, and allowing the mixture to gel. In
certain embodiments, the molar ratio of the electrophilic groups to
the nucleophilic groups in the PEG precursors is about 1:1, but the
nucleophilic groups (such as the amine groups) may also be used in
excess of the electrophilic groups. Other precursors, including
other electrophilic group-containing precursors and other
nucleophilic group-containing precursors or crosslinking agents may
be used as disclosed in the section "The polymer network" and the
section "PEG hydrogels" herein.
[0280] In certain embodiments, a mixture of the electrophilic
group-containing precursor, the nucleophilic group-containing
precursor or other crosslinking agent, the TKI and optionally
buffer (and optionally additional ingredients as disclosed in the
section "Additional ingredients") is prepared. This may happen in a
variety of orders, including but not limited to first preparing
separate mixtures of the electrophilic and the nucleophilic
group-containing precursors each in buffer solution, then combining
one of the buffer/precursor mixtures, such as the
buffer/nucleophilic group-containing precursor mixture, with the
TKI and subsequently combining this TKI-containing buffer/precursor
mixture with the other buffer/precursor mixture (in this case the
buffer/electrophilic group-containing precursor mixture). After a
mixture of all components has been prepared (i.e., after all
components have been combined and the wet composition has been
formed), the mixture is cast into a suitable mold or tubing prior
to complete gelling of the hydrogel in order to provide the desired
final shape of the hydrogel. The mixture is then allowed to gel.
The resulting hydrogel is then dried.
[0281] The viscosity of the wet hydrogel composition to be cast
into a mold or tubing may depend inter alia on the concentration
and the solids content of the hydrogel composition, but may also
depend on external conditions such as the temperature. Castability
of the wet hydrogel composition especially in case the composition
is cast into fine-diameter tubing, may be improved by decreasing
the viscosity of the wet composition, including (but not limited
to) decreasing the concentration of ingredients in the solvent
and/or decreasing the solids content, or other measures such as
increasing the temperature etc. Suitable solids contents are
disclosed herein in the section "Formulation".
[0282] In case the implant should have the final shape of a fiber
(such as a cylinder), the reactive mixture may be cast into a fine
diameter tubing (of e.g. an inner diameter of about 1.0 mm to about
1.5 mm), such as a PU or silicone tubing, in order to provide for
the extended cylindrical shape. Different geometries and diameters
of the tubing may be used, depending on the desired final
cross-sectional geometry of the hydrogel fiber, its initial
diameter (which may still be decreased by means of stretching), and
depending also on the ability of the reactive mixture to uniformly
fill the tubing.
[0283] Thus, the inside of the tubing may have a round geometry or
a non-round geometry, such as a cross-shaped (or other) geometry.
By means of a cross-shaped geometry, the surface of the implant may
be increased. Also, in certain embodiments, the amount of TKI
incorporated in the implant may be increased with such cross-shaped
geometry. Overall, by using a cross-shaped geometry, release of the
API from the implant may in certain embodiments be increased. Other
cross-sectional geometries of the implant may be used as disclosed
herein.
[0284] In certain embodiments, after the hydrogel has formed and
has been left to cure to complete gelling, the hydrogel strand may
be longitudinally stretched in the wet or dry state as already
disclosed in detail herein e.g. in the section relating to the
dimensional change of the implant upon hydration. In certain
embodiments, a stretching factor (also referred to herein as
"stretch factor") may be in a range of about 1 to about 4.5, or
about 1.3 to about 3.5, or about 2 to about 2.5, or within other
ranges also as disclosed herein (e.g. in, but not limited to, the
section "Dimensions of the implant and dimensional change upon
hydration through stretching". The stretch factor indicates the
ratio of the length of a certain hydrogel strand after stretching
to the length of the hydrogel strand prior to stretching. For
example, a stretch factor of 2 for dry stretching means that the
length of the dry hydrogel strand after (dry) stretching is twice
the length of the dry hydrogel strand before the stretching. The
same applies to wet stretching. When dry stretching is performed in
certain embodiments, the hydrogel is first dried and then
stretched. When wet stretching is performed in certain embodiments,
the hydrogel is stretched in the wet (undried) state and then left
to dry under tension. Optionally, heat may be applied upon
stretching. Further optionally, the hydrogel fiber may additionally
be twisted. In certain embodiments, the stretching and/or drying
may be performed when the hydrogel is still in the tubing.
Alternatively, the hydrogel may be removed from the tubing prior to
being stretched. In certain embodiments, the implant maintains its
dimensions even after stretching as long as it is kept in the dry
state at or below room temperature.
[0285] After stretching and drying the hydrogel strand is removed
from the tubing (if still located inside the tubing) and cut into
segments of a length desired for the final implant in its dry
state, such as disclosed herein (if cut within the tubing, the cut
segments are removed from the tubing after cutting). A particularly
desired length of the implant in the dry state for the purposes of
the present invention is for example a length of equal to or less
than about 12 mm, or equal to or less than about 10 mm, as
disclosed herein.
[0286] In certain embodiments, the final prepared implant is then
loaded into a fine diameter needle. In certain embodiments, the
needle has a gauge size of from 22 to 30, such as gauge 22, gauge
23, gauge 24, gauge 25, gauge 26, gauge 27, gauge 28, gauge 29 or
gauge 30. In specific embodiments, the needle is a 25- or 27-gauge
needle, or an even smaller gauge needle, such as a 30-gauge needle,
depending on the diameter of the dried (and optionally stretched)
implant.
[0287] In certain embodiments, the needles containing implant are
then separately packaged and sterilized e.g. by means of gamma
irradiation.
[0288] In certain embodiments, an injection device, such as a
syringe or another injection device, may be separately packaged and
sterilized e.g. by means of gamma irradiation as disclosed below
for the kit (which is another aspect of the present invention, see
the section "Injection device and kit").
[0289] A particular embodiment of a manufacturing process according
to the invention is disclosed in detail in Example 1.
(PEG) Tipping the Needle:
[0290] In one embodiment, after the implant has been loaded into
the needle the tip of the needle is dipped into a melted
low-molecular weight PEG. Alternatively, molten PEG may be injected
or placed/dripped into the needle tip lumen. This low-molecular PEG
is liquid (molten) at body temperature, but solid at room
temperature. After applying the molten PEG to the needle tip,
either by dipping or dripping, upon cooling the needle a hardened
small drop or section (also referred to herein as "tip") of PEG
remains at and in the top of the needle which occludes the needle
lumen. The location of this tip/plug is shown in FIG. 25B.
[0291] The low-molecular weight PEG used in this embodiment may be
a linear PEG and may have an average molecular weight of up to
about 1500, or up to about 1000, or may have an average molecular
weight of about 400, about 600, about 800 or about 1000. Also
mixtures of PEGs of different average molecular weights as
disclosed may be used. In specific embodiments the average
molecular weight of the PEG used for this purpose of tipping the
needle is about 1000. This 1k (1000) molecular weight PEG has a
melting point between about 33.degree. C. and about 40.degree. C.
and melts at body temperature when the needle is injected into the
eye.
[0292] Alternatively to the PEG materials, any other material for
tipping the injection needle may be used that is water soluble and
biocompatible (i.e., that may be used in contact with the human or
animal body and does not elicit topical or systemic adverse
effects, e.g. that is not irritating) and that is solid or hardened
at room temperature but liquid or substantially liquid or at least
soft at body temperature. Alternatively to PEG, also the following
materials may e.g. be used (without being limited to these):
poloxamers or poloxamer blends that melt/are liquid at body
temperature; crystallized sugars or salts (such as trehalose or
sodium chloride), agarose, cellulose, polyvinyl alcohol,
poly(lactic-co-glycolic acid), a UV-curing polymer, chitosan or
combinations of mixtures thereof.
[0293] The plug or tip aids in keeping the implant in place within
the needle during packaging, storage and shipping and also further
protects the implant from prematurely hydrating during handling as
it occludes the needle lumen. It also prevents premature
rehydration of the implant within the needle due to moisture
ingress during the administration procedure, i.e., during the time
the physician prepares the needle and injector for administration,
and also at the time when the implant is about to be injected and
the needle punctures into the eye (as the positive pressure in the
eye could cause at least some premature hydration of the implant
just before it is actually injected). The tip or plug additionally
provides lubricity when warmed to body temperature and exposed to
moisture and thereby allows successful deployment of the implant.
Moreover, by occluding the needle lumen, the needle tipping
minimizes the potential for tissue injury, i.e., tissue coring, a
process by which pieces of tissue are removed by a needle as it
passes through the tissue.
[0294] In order to apply the PEG (or other material) tip/plug to
the needle lumen, in one embodiment the needle containing the
implant may be manually or by means of an automated apparatus
dipped into a container of molten PEG (or the respective other
material). The needle may be held dipped in the molten material for
a few seconds to enable the molten material to flow upward into the
needle through capillary action. The dwell time, the dip depth and
the temperature of the molten material determine the final size or
length of the tip/plug. In certain embodiments, the length of the
PEG (or other) tip/plug at the top end of the needle may be from
about 1 to about 5 mm, such as from about 2 to about 4 mm. In
certain embodiments, in case a 1k PEG is used the weight of the
tip/plug may be from about 0.1 mg to about 0.6 mg, such as from
about 0.15 mg to about 0.55 mg. It was demonstrated that implants
according to the present invention can be successfully deployed in
vivo and in vitro from an injector carrying a needle with a 1k PEG
tip as disclosed herein.
[0295] The tipping of an injection needle as disclosed herein may
also be used for the injection of other implants or other
medicaments or vaccines to be injected into the human or animal
body (including other locations within the eye, or other areas or
tissue of the body) by means of a needle, where the effect of
protection of the implant (or medicament or vaccine) from moisture
and the protective effect on tissue into which the implant (or
medicament or vaccine) is injected is desirable and
advantagoues.
Stretching:
[0296] The shape memory effect of the stretching has already been
disclosed in detail above with respect to the properties of the
implant. In certain embodiments, the degree of shrinking upon
hydration depends inter alia on the stretch factor as already
disclosed above.
[0297] In certain embodiments, the present invention thus also
relates to a method of imparting shape memory to a hydrogel strand
comprising an active agent dispersed in the hydrogel by stretching
the hydrogel strand in the longitudinal direction.
[0298] Likewise, in certain embodiments, the present invention thus
also relates to a method of manufacturing an ocular implant
comprising a hydrogel comprising an active agent dispersed therein,
wherein the implant changes its dimensions upon administration to
the eye, the method comprising preparing a strand of the hydrogel
and stretching it in the longitudinal direction.
[0299] Stretch factors for use in these methods of the invention
may be utilized as already disclosed above. The described method of
manufacture including the stretching methods are not limited to
implants comprising TKI inhibitors or axitinib, but may also be
used for hydrogels comprising other active pharmaceutical agents,
or for implants comprising hydrogels that are not formed from PEG
units, but from other polymer units as disclosed herein above that
are capable of forming a hydrogel.
[0300] In embodiments where the implant contains axitinib in an
amount in a range from about 160 .mu.g to about 250 .mu.g, or in an
amount of about 200 .mu.g, the stretching may be performed after
drying the hydrogel by a stretch factor of about 2 to about 5, or a
stretch factor of about 3 to about 4.5 (dry stretching).
[0301] In certain embodiments where the implant contains axitinib
in an amount in a range from about 480 .mu.g to about 750 .mu.g, or
in an amount of about 600 .mu.g, the stretching may be performed in
a wet state prior to drying the hydrogel by a stretch factor of
about 0.5 to about 5, or a stretch factor of about 1 to about 4, or
a stretch factor of about 1.3 to about 3.5, or a stretch factor of
about 1.7 to about 3, or a stretch factor of about 2.0 to 2.5 (wet
stretching).
III. Injection Device and Kit
[0302] In certain embodiments, the present invention is further
directed to a kit (which may also be referred to as a "system")
comprising one or more sustained release biodegradable ocular
implant(s) as disclosed above or manufactured in accordance with
the methods as disclosed above and one or more needle(s) for
injection, wherein the one or more needle(s) is/are each pre-loaded
with one sustained release biodegradable ocular implant in a dried
state. In certain embodiments the needle(s) has a gauge size of
from 22 to 30, such as 22, 23, 24, 25, 26, 27, 28, 29, or 30 gauge.
In specific embodiments, the neeles may be 25- or 27-gauge
needle(s) or may be smaller gauge, such as 30-gauge needle(s). The
diameter of the needle is chosen based on the final diameter of the
implant in the dried (and optionally stretched) state. The active
contained in the implant is generally a TKI, such as axitinib.
[0303] In one embodiment the kit comprises one or more, such as two
or three 22- to 30-gauge, such as 25- or 27-gauge needle(s) each
loaded with an implant containing axitinib in an amount in the
range from about 180 .mu.g to about 220 .mu.g, or in an amount of
about 200 .mu.g.
[0304] In yet another embodiment the kit comprises one 25-gauge
needle loaded with an implant containing axitinib in an amount in
the range from about 540 .mu.g to about 660 .mu.g, or in an amount
of about 600 .mu.g. In another embodiment, the kit comprises one
27-gauge needle loaded with an implant containing axitinib in an
amount in the range from about 540 .mu.g to about 660 .mu.g, or in
an amount of about 600 .mu.g.
[0305] If two or more implants are contained in the kit, these
implants may be identical or different, and may contain identical
or different doses of TKI.
[0306] In certain embodiments, the lumen of the needle containing
the implant may be occluded by a material that is solid at room
temperature but soft or liquid at body temperature, such as a 1k
PEG material, as disclosed herein in detail in the section
"Manufacture of the Implant" and specifically the subsection "(PEG)
Tipping the needle" thereof.
[0307] The kit may further contain an injection device for
injecting the implant(s) into the eye of a patient, such as into
the vitreous humor of the patient. In certain embodiments the
injection device is provided and/or packaged separately from the
one or more needle(s) loaded with implant. In such embodiments the
injection device must be connected to the one or more needle(s)
loaded with implant prior to injection.
[0308] In certain embodiments the number of injection devices
provided separately in the kit equals the number of needles loaded
with the implant provided in the kit. In these embodiments the
injection devices are only used once for injection of one
implant.
[0309] In other embodiments the kit contains one or more injection
device(s) for injecting the implant into the eye of a patient, such
as into the vitreous humor of the patient, wherein each injection
device is or is not pre-connected to a needle loaded with implant.
The present invention thus in one aspect also relates to a
pharmaceutical product comprising a sustained release biodegradable
ocular implant loaded in a needle and an injection device, wherein
the needle is pre-connected to the injection device. In case the
needle is not yet pre-connected to the injection device, the
physician administering the implant needs to remove both the needle
containing the implant and the injection device from the packaging,
and connect the needle to the injection device to be able to inject
the implant into the patient's eye.
[0310] In some embodiments the injection device contains a push
wire to deploy the implant from the needle into the vitreous humor.
The push wire may be a Nitinol push wire or may be a stainless
steel/Teflon push wire. The push wire allows deploying the implant
from the needle more easily.
[0311] In other embodiments the injection device and/or the
injection needle may contain a stop feature that controls the
injection depth.
[0312] In some embodiments the injection device is or comprises a
modified Hamilton glass syringe that may be placed into a plastic
syringe housing, such as inside an injection molded housing. A push
wire, such as a Nitinol wire, is inserted into the syringe and
advances with the plunger of the syringe during deployment of the
implant. To facilitate entry of the nitinol push wire into the
needle, a hub insert may be added into the needle hub. FIGS. 25A
and 25B show one embodiment of an injector according to the present
invention for injecting an implant into the vitreous humor of a
patient. This depicted embodiment of an injector comprises a
Hamilton syringe body and a Nitinol push wire to deploy the
implant. FIG. 25A shows the Hamilton syringe body inside of an
injection molded casing. FIG. 25B shows a schematic view of the
components of this embodiment of the injector. In certain
embodiments, the injector comprising the Hamilton syringe body and
the plastic housing parts are pre-assembled in a kit according to
the invention and the injector is ready for use (without or without
mounted needle containing the implant). In other embodiments, the
injector must be assembled by the physician prior to mounting the
needle containing the implant.
[0313] In other embodiments, the injection device is an injection
molded injector. A schematic exploded view of an embodiment of such
injection molded injector is shown in FIG. 26. In this case the
number of assembly steps by the physician just prior to
administering the implant to a patient is reduced.
[0314] The kit may further comprise one or more doses, in
particular one dose, of an anti-VEGF agent ready for injection. The
anti-VEGF agent may be selected from the group consisting of
aflibercept, bevacizumab, pegaptanib, ranibizumab, and
brolucizumab. In certain embodiments the anti-VEGF agent is
bevacizumab. In other embodiments the anti-VEGF agent is
aflibercept. The anti-VEGF agent may be provided in a separate
injection device connected to a needle, or may be provided as a
solution or suspension in a sealed vial, from which the solution or
suspension may be aspirated through a needle into a syringe or
other injection device prior to administration.
[0315] The kit may further comprise an operation manual for the
physician who is injecting the ocular implant(s). The kit may
further comprise a package insert with product-related
information.
[0316] In addition to the kit, the present invention in one aspect
is also directed to an injection device per se that is suitable for
injecting a sustained release biodegradable ocular implant
according to the invention into the eye. The injection device may
contain means for connecting the injection device to a needle,
wherein the needle is pre-loaded with the implant. The injection
device may further contain a push wire to deploy the implant from
the needle into the eye when the injection device has been
connected to the needle, which push wire may be made of Nitinol or
stainless steel/Teflon or another suitable material. The injection
device may further be obtainable by affixing the wire to the
plunger and encasing it between two snap fit injector body parts
and securing the plunger with a clip. An injection device and a
needle pre-loaded with implant in accordance with certain
embodiments of the present invention is depicted in FIG. 1.
[0317] As illustrated in FIG. 1, in some embodiments, the injection
device (e.g., implant injector device) may include a first assembly
and a second assembly that are packaged separately (e.g., in
separate enclosures). FIG. 26C is an exploded view of the first
assembly and FIG. 26D is an exploded view of the second
assembly.
[0318] Referring to FIG. 26C, the first assembly includes a body
forming a first interior volume, a plunger including a first distal
end disposed within the first interior volume, a wire including a
first distal end secured to the first distal end of the plunger,
and a plunger clip. The plunger clip is configured to interface
with the plunger and the body to prevent actuation of the plunger.
The body may include a first body half and a second body half
configured to interconnect with each other. The body may include a
living hinge that interfaces with a protrusion of the plunger
resposnive to actuation of the plunger. The living hinge may allow
actuation of the plunger responsive to application of a threshold
force.
[0319] Referring the FIG. 26D, the second assembly includes a cowl
forming a second interior volume, a needle including a base and a
lumen, a cowl cap disposed within the base, and a needle shiled
configured to secure to the cowl and to be disposed around a
portion of the lumen. An implant is configured to be disposed
within the lumen of the needle. The cowl may include a first cowl
half and a second cowl half configured to interconnect with each
other. The second assembly may further include a polymer tip (e.g.,
PEG tip) disposed on a second distal end of the lumen. The implant
is secured in the lumen between the cowl cap and the polymer tip.
The polymer tip is configured to liquefy (e.g., dissolve) within a
user to allow the implant to be injected into the user.
[0320] In some embodiments, the second assembly is made from
materials that include less moisture and/or undergoes conditioning
(e.g., nitrogen conditioning) prior to being sealed in an enclosure
to prevent the implant from absorbing moisture. In some
embodiments, the first assembly is made from materials that include
more moisture and/or does not undergo conditioning prior to being
sealed in an enclosure since the implant is not included in the
enclosure with the first assembly.
[0321] The first assembly may be removed from a first enclosure of
FIG. 1 and a second assembly may be removed from a second enclosure
of FIG. 1. Referring to FIG. 26E, the first assembly and the second
assembly may be aligned. One or more exterior recesses of the first
assembly may align with one or more interior protrusions of the
second assembly. The first assembly and second assembly may include
markings (e.g., arrows) to indicate how to align the first assembly
and the second assembly. Referring to FIG. 26F, the cowl of the
second assembly is secured to the body of the first assembly (e.g.,
via the interior protrusions of the cowl entering the exterior
recesses of the body). Referring to FIG. 26G, the needle shield is
removed from the cowl of the second assembly and the plunger clip
is removed from the body and plunger of the first assembly.
Referring to FIG. 26H, the plunger of the first assembly is
actuated (e.g., pushed into the body of the first assembly) to
deploy the implant from the lumen of the needle of the second
assembly. In some embodiments, the body has a living hinge that
allows actuation of the plunger responsive to a threshold force
being applied to the plunger. In some embodiments, the lumen of the
needle has a polymer tip (e.g., a polymer, such as PEG, disposed at
least in the distal end of the lumen) blocking the implant from
being deployed from the lumen. Insertion of the lumen with a
polymer tip into a user may prevent coring of tissue of the user
(e.g., cutting a piece of tissue the diameter of the inside of the
lumen to later be deployed into the user). The lumen may be
inserted in a user for a threshold amount of time (e.g., 1 to 5
seconds) to liquefy (e.g., dissolve) the polymer tip. After the
polymer tip is liquefied, the implant may be deployed from the
lumen via actuation of the plunger.
IV. Therapy
[0322] In certain embodiments, the present invention is further
directed to a method of treating an ocular disease in a patient in
need thereof, the method comprising administering to the patient
the sustained release biodegradable ocular implant comprising the
hydrogel and the tyrosine kinase inhibitor as disclosed above.
[0323] In specific embodiments, the present invention is directed
to a method of treating an ocular disease in a patient in need
thereof, the method comprising administering to the patient a
sustained release biodegradable ocular implant comprising a
hydrogel and at least about 150 .mu.g of a tyrosine kinase
inhibitor (TKI), wherein TKI particles are dispersed within the
hydrogel.
[0324] In this treatment, the dose per eye administered once for a
treatment period of at least 3 months is at least about 150 .mu.g,
such as from about 150 .mu.g to about 1800 .mu.g, or from about 150
.mu.g to about 1200 .mu.g of the tyrosine kinase inhibitor. In
certain preferred embodiments the tyrosine kinase inhibitor is
axitinib.
[0325] In certain embodiments the dose of the TKI, and specifically
of axitinib, administered per eye once for (i.e., during) the
treatment period is in the range of about 200 .mu.g to about 800
.mu.g. In certain embodiments the dose is in the range from about
160 .mu.g to about 250 .mu.g, or from about 180 .mu.g to about 220
.mu.g, or of about 200 .mu.g. In yet other specific embodiments
this dose is in the range from about 320 .mu.g to about 500 .mu.g,
or from about 360 .mu.g to about 440 .mu.g, or of about 400 .mu.g.
In yet other embodiments this dose is in the range from about 480
.mu.g to about 750 .mu.g, or from about 540 .mu.g to about 660
.mu.g, or of about 600 .mu.g. In yet other embodiments this dose is
in the range from about 640 .mu.g to about 1000 .mu.g, or from
about 720 .mu.g to about 880 .mu.g, or of about 800 .mu.g. In yet
other embodiments this dose is in the range from about 800 .mu.g to
about 1250 .mu.g, or from about 900 .mu.g to about 1100 .mu.g, or
of about 1000 .mu.g. In yet other embodiments this dose is in range
from about 960 .mu.g to about 1500 .mu.g, or from about 1080 .mu.g
to about 1320 .mu.g, or of about 1200 .mu.g. In particular
embodiments, the dose administered per eye once for the treatment
period is about 600 .mu.g axitinib. In particular embodiments, this
dose of 600 .mu.g is contained in one single implant.
[0326] In certain embodiments, the treatment period for the
treatment of an ocular disease as disclosed herein with an implant
of the present invention is least 3 months, at least 4.5 months, at
least 6 months, at least 9 months, at least 11 months, at least 12
months, at least 13 months, at least 14 months or even longer, and
may for example be about 6 to about 9 months.
[0327] In certain embodiments the ocular disease involves
angiogenesis.
[0328] In other embodiments the ocular disease may be mediated by
one or more receptor tyrosine kinases (RTKs), such as VEGFR-1,
VEGFR-2, VEGFR-3, PDGFR-.alpha./.beta., and/or by c-Kit.
[0329] In some embodiments the ocular disease is a retinal disease
including Choroidal Neovascularization, Diabetic Retinopathy,
Diabetic Macula Edema, Retinal Vein Occlusion, Acute Macular
Neuroretinopathy, Central Serous Chorioretinopathy, and Cystoid
Macular Edema; wherein the ocular disease is Acute Multifocal
Placoid Pigment Epitheliopathy, Behcet's Disease, Birdshot
Retinochoroidopathy, Infectious (Syphilis, Lyme, Tuberculosis,
Toxoplasmosis), Intermediate Uveitis (Pars Planitis), Multifocal
Choroiditis, Multiple Evanescent White Dot Syndrome (MEWDS), Ocular
Sarcoidosis, Posterior Scleritis, Serpignous Choroiditis,
Subretinal Fibrosis, Uveitis Syndrome, or Vogt-Koyanagi-Harada
Syndrome; wherein the ocular disease is a vascular disease or
exudative diseases, including Coat's Disease, Parafoveal
Telangiectasis, Papillophlebitis, Frosted Branch Angitis, Sickle
Cell Retinopathy and other Hemoglobinopathies, Angioid Streaks, and
Familial Exudative Vitreoretinopathy; or wherein the ocular disease
results from trauma or surgery, including Sympathetic Ophthalmia,
Uveitic Retinal Disease, Retinal Detachment, Trauma, Photodynamic
Laser Treatment, Photocoagulation, Hypoperfusion During Surgery,
Radiation Retinopathy, or Bone Marrow Transplant Retinopathy.
[0330] In alternative embodiments the sustained release
biodegradable ocular implant comprising the hydrogel and the
tyrosine kinase inhibitor of the present invention can be applied
in treating ocular conditions associated with tumors. Such
conditions include e.g., Retinal Disease Associated with Tumors,
Solid Tumors, Tumor Metastasis, Benign Tumors, for example,
hemangiomas, neurofibromas, trachomas, and pyogenic granulomas,
Congenital Hypertrophy of the RPE, Posterior Uveal Melanoma,
Choroidal Hemangioma, Choroidal Osteoma, Choroidal Metastasis,
Combined Hamartoma of the Retina and Retinal Pigmented Epithelium,
Retinoblastoma, Vasoproliferative Tumors of the Ocular Fundus,
Retinal Astrocytoma, or Intraocular Lymphoid Tumors.
[0331] In general, the ocular implants of the present invention can
also be applied for treatment of any ocular disease involving
vascular leakage.
[0332] In certain embodiments the ocular disease is one selected
from the list consisting of neovascular age-related macular
degeneration (AMD), diabetic macula edema (DME), and retinal vein
occlusion (RVO). In particular embodiments the ocular disease is
neovascular age-related macular degeneration.
[0333] In some embodiments the treatment is effective in reducing
the central subfield thickness (CSFT) as measured by optical
coherence tomography in a patient whose central subfield thickness
is elevated. Elevated within that context means that the CSFT is
higher in the patient when compared to other individuals not
suffering from the specific ocular disease. The elevated CSFT may
be caused by retinal fluid such as sub- or intraretinal fluid. The
reduction of CSFT in a patient may be determined with respect to a
baseline CSFT measured in that patient prior to the start of the
treatment, i.e., prior to the administration of the implant of the
present invention. The capacity of the implants of the present
invention to reduce CSFT and to maintain or to substantially
maintain a reduced CSFT over an extended period of time in a cohort
of patients is demonstrated in Example 6.3 and 6.4. In other
embodiments, by means of the treatment according to the present
invention involving the administration of an implant according to
the present invention the CSFT of a patient whose CSFT is elevated
due to an ocular disease involving angiogenesis is essentially
maintained at a certain given level, or a clinically significant
increase of the CSFT is prevented in the patient while sub- or
intraretinal fluid is not substantially increased, i.e., is also
essentially maintained.
[0334] In a particular embodiment, the CSFT is reduced in a patient
and maintained at a reduced level over a period of at least 3
months, at least 4.5 months, at least 6 months, at least 9 months,
at least 11 months, at least 12 months, at least 13 months, at
least 14 months or even longer after administration of the implant
of the invention. In a very particular embodiment, the CSFT is
reduced for at least 6 months or at least 9 months or at least 12
months after administration of the implant with respect to the
baseline CSFT of that patient prior to administration of the
implant. In other particular embodiments, a reduced amount of
retinal fluid and/or a reduced CSFT is maintained in a patient over
a treatment period of at least 3 months, at least 4.5 months, at
least 6 months, at least 9 months, at least 11 months, at least 12
months, at least 13 months, at least 14 months or even longer after
administration of the implant of the invention without the need for
administration of rescue medication (such as an injection of an
anti-VEGF agent), or wherein rescue medication is administered only
rarely, such as 1, 2, or 3 times during the treatment period. Thus,
in this embodiment, during the treatment period with an implant
according to the present invention the patient receiving the
treatment may not need any rescue medication, or the administration
of rescue medication is only required rarely, such as 1, 2 or 3
times during the treatment period.
[0335] In certain embodiments, the rescue medication is an
anti-VEGF agent, such as aflibercept or bevacizumab, that is
administered in the form of a suspension or solution by means of
intravitreal injection. In certain specific embodiments, the rescue
medication is one dose (2 mg) of aflibercept, administered by means
of intravitreal injection. In line with the definitions herein,
concurrent (i.e., planned) administration of an anti-VEGF agent
together with an implant according to another embodiment of the
present invention disclosed herein does not constitute a "rescue
medication". In more particular embodiments, the treatment period
wherein the level of fluid and/or the CSFT (as reduced by means of
the administration of an implant according to the invention) is
maintained or essentially maintained without the administration of
rescue medication (or with rescue medication administered only
rarely) is from about 6 to about 9 months after administration of
the implant. In certain embodiments, the patients treated with an
implant according to the invention do not require the concomitant
administration of steroids (e.g., dexamethasone or prednisolone
drops) during the treatment period.
[0336] In another embodiment, by means of the treatment according
to the present invention involving the administration of an implant
according to the present invention the CSFT of a patient whose CSFT
is elevated due to angiogenesis is reduced, essentially maintained,
or a clinically significant increase of the CSFT is prevented while
the patient's vision (e.g. expressed by means of the best corrected
visual acuity, also referred to herein as "BCVA") is not impaired,
or is not significantly impaired. In certain embodiments, by means
of the treatment according to the present invention involving the
administration of an implant according to the present invention a
patient's vision (where the patient's vision is impaired due to an
ocular disease involving angiogenesis) as e.g. expressed by the
BCVA may improve during the treatment period of at least 3 months,
at least 6 months, at least 9 months, at least 11 months, at least
12 months, at least 13 months or at least 14 months.
[0337] Thus, in certain embodiments the present invention provides
a method of improving the vision of a patient whose vision is
impaired e.g. due to retinal fluid caused by an ocular disease
involving angiogenesis, wherein the method comprises administering
an implant according to the invention to the patient, such as by
means of intravitreal injection. The improvement of the vision of a
patient may be assessed for instance by means of the BCVA. An
improvement of vision may manifest itself by an increase of the
patient's BCVA e.g. by at least 10, or at least 15, or at least 20
ETDRS letters.
[0338] In certain embodiments, the total dose of TKI, such as
axitinib, per eye administered once for the treatment period may be
contained in one or more implants. In certain embodiments the dose
per eye administered once for the treatment period is contained in
one implant as for instance in one implant comprising a dose of
about 600 .mu.g or of about 200 .mu.g axitinib. In other
embodiments the total dose per eye administered once for the
treatment period is contained in e.g. two implants, wherein each
implant comprises a dose of e.g. about 200 .mu.g axitinib
(resulting in a total dose of about 400 .mu.g in that case). In yet
other embodiments the dose per eye administered once for the
treatment period is contained in e.g. three implants, wherein each
implant comprises a dose of e.g. about 200 .mu.g axitinib
(resulting in a total dose of about 600 .mu.g in that case). In
particular embodiments of the methods of treatment of the present
invention, the dose of axitinib administered to one eye is about
600 .mu.g and is contained in one implant.
[0339] For the injection of implants according to the present
invention into the eye, such as into the vitreous humor, of a
patient in the course of a treatment of an ocular disease, such as
a retinal disease, including AMD, it is generally desirable to use
implants having a therapeutically effective dose of TKI (i.e., one
that is appropriate in view of particular patient's type and
severity of condition) in a relatively small implant in order to
facilitate administration (injection) as well as to reduce possible
damage to ocular tissue as well as a possible impact of the
patient's vision while the implant is in place. The implants of the
present invention advantageously combine the benefits of a suitably
high dose of the TKI (i.e., a therapeutically effective dose
adjusted to a particular patient's need) with a relatively small
implant size.
[0340] In certain embodiments, the implant may be administered by
means of an injection device according to the present invention
connected to a needle pre-loaded with implant as disclosed herein,
or may be administered by means of another injection device
suitable to be connected to a needle pre-loaded with an implant as
disclosed herein, such as a (modified) Hamilton syringe. In other
embodiments, a hollow microneedle may be used for suprachoroidal
administration as disclosed in U.S. Pat. No. 8,808,225 which is
incorporated by reference herein.
[0341] In embodiments wherein two or more implants are
administered, the implants are generally administered concurrently
as disclosed herein above. The implants administered concurrently
can be the same or different. In cases where an administration
during the same session is not possible e.g. due to administration
complications or patient-related reasons a successive
administration during two or more different sessions may
alternatively be applied, such as for instance administration of
two implants 7 days apart. This may still be considered as a
"concurrent" administration in the context of the present
invention.
[0342] In certain embodiments the dry implants are loaded in a
needle, such as a needle with a gauge siz of from 22 to 23, such as
a 25-gauge or a 27-gauge needle, or a smaller gauge needle, for
injection and are administered to the eye, e.g. to the vitreous
humor, through this needle. In one embodiment, the injector used
for injecting the implant into the eye is an injection device
according to another aspect of the present invention as disclosed
above. Implants containing 200 .mu.g and 600 .mu.g, respectively,
that are suitable for the therapeutic applications according to the
present application are exemplarily presented in Tables 21.1 and
21.2.
[0343] The implant can generally be administered by means of
intravitreal, subconjunctival, subtenon, suprachoroidal, or
intracameral injection. In certain embodiments the implant is
administered to the vitreous humor, e.g. the implant is
administered intravitreally into the posterior section of the
vitreous humor. In other embodiments, the implant is administered
by means of a hollow microneedle, such as into the sclera of the
eye at an insertion site into the suprachoroidal space of the eye
as disclosed in U.S. Pat. No. 8,808,225, which is incorporated
herein by reference.
[0344] In certain embodiments, the treatment period is at least 3
months, but may be at least 4.5 months, at least 6 months, at least
9 months, at least 11 months or at least 12 months. In particular
embodiments, the treatment period is at least 6 months, at least 9
months, at least 11 months, at least 12 months, at least 13 months,
or at least 14 months. In certain embodiments, the treatment period
may also be longer, such as up to about 15 months. "Treatment
period" according to one embodiment of the invention means that a
certain therapeutic effect of an implant of the present invention
once administered is maintained, essentially maintained or
partially maintained over that period of time. In other words, only
one injection (of the implant of the present invention) is required
in certain embodiments for maintaining a therapeutic effect of
reducing or essentially maintaining or of preventing a clinically
significant increase of the CSFT during the extended period of time
referred to herein as "treatment period". This is a considerable
advantage over currently used anti-VEGF treatments for AMD which
require more frequent administration, and thus improves the
patient's quality of life. Another advantage is that the necessity
and/or frequency of the administration of rescue medication during
the treatment period is very low. In certain embodiments, no rescue
medication is necessary during the treatment period, such as a
treatment period of from about 6 to about 9 months after
administration of the implant. In certain other embodiments, rescue
medication only has to be administered rarely, such as 1, 2 or 3
times during the treatment period. The vision of a patient may be
improved as evidenced e.g. by an increase in the BCVA (such as by
at least 10, at least 15 or at least 20 ETDRS letters) following
administration of an implant of the invention.
[0345] In one particular embodiment the invention is directed to a
method of treating neovascular age-related macular degeneration in
a patient in need thereof, the method comprising administering to
the patient a sustained release biodegradable ocular implant
comprising a hydrogel that comprises a polymer network and about
200 .mu.g of a tyrosine kinase inhibitor, wherein one implant per
eye is administered once for a treatment period of at least 9
months, and wherein the patient has a history of an anti-VEGF
treatment. In this embodiment the treatment results in a reduction
in central subfield thickness (CSFT), or at least maintenance of
CSFT, as measured by optical coherence tomography during the
treatment period. In this embodiment the TKI may further be
axitinib, which is dispersed in the hydrogel which comprises a
polymer network formed by reacting 4a20kPEG-SAZ with
8a20kPEG-NH.sub.2, and wherein the implant is in a dried state
prior to administration. In this embodiment the hydrogel when
formed and before being dried contains about 7.5% polyethylene
glycol, representing the polyethylene glycol weight divided by the
fluid weight.times.100. Alternatively, the patient treated may also
have no history of an anti-VEGF treatment (AMD treatment
naive).
[0346] In another particular embodiment the invention is directed
to a method of treating neovascular age-related macular
degeneration in a patient in need thereof, the method comprising
administering to the patient a sustained release biodegradable
ocular implant comprising a hydrogel that comprises a polymer
network and about 200 .mu.g of a tyrosine kinase inhibitor, wherein
two implants per eye forming a total dose of about 400 .mu.g are
administered once for a treatment period of at least 3 months, or
for at least 9 months, and wherein the patient has a history of an
anti-VEGF treatment or has no history of an anti-VEGF treatment
(AMD treatment naive). In this embodiment the treatment results in
a reduction (or at least maintenance of) central subfield thickness
(CSFT) as measured by optical coherence tomography during the
treatment period. In this embodiment the TKI may further be
axitinib which is dispersed in the hydrogel which comprises a
polymer network formed by reacting 4a20kPEG-SAZ with
8a20kPEG-NH.sub.2, and wherein the implant is in a dried state
prior to administration. In this embodiment the hydrogel when
formed and before being dried contains about 7.5% polyethylene
glycol, representing the polyethylene glycol weight divided by the
fluid weight.times.100.
[0347] In yet another particular embodiment the invention is
directed to a method of treating neovascular age-related macular
degeneration in a patient in need thereof, the method comprising
administering to the patient a sustained release biodegradable
ocular implant comprising a hydrogel that comprises a polymer
network and about 200 .mu.g of a tyrosine kinase inhibitor, wherein
three implants per eye forming a total dose of about 600 .mu.g are
administered once for a treatment period of at least 3 months, or
for at least 9 months, and wherein the patient has a history of an
anti-VEGF treatment or has no history of an anti-VEGF treatment
(AMD treatment naive). In this embodiment the treatment results in
a reduction (or at least maintenance of) central subfield thickness
(CSFT) as measured by optical coherence tomography during the
treatment period. In this embodiments the TKI may further be
axitinib which is dispersed in the hydrogel which comprises a
polymer network formed by reacting 4a20kPEG-SAZ with 8a20kPEG-NH2,
and wherein the implant is in a dried state prior to
administration. In this embodiment the hydrogel when formed and
before being dried contains about 7.5% polyethylene glycol,
representing the polyethylene glycol weight divided by the fluid
weight.times.100.
[0348] In yet other embodiments the invention is directed to a
method of treating neovascular age-related macular degeneration in
a patient in need thereof, the method comprising administering to
the patient a sustained release biodegradable ocular implant
comprising axitinib in an amount in the range from about 480 .mu.g
to about 750 .mu.g dispersed in a hydrogel comprising a polymer
network, wherein the implant is administered once for a treatment
period of at least 3 months. In certain of these embodiments the
axitinib is contained in the implant in an amount of from about 560
.mu.g to about 660 .mu.g, or of about 600 .mu.g. For specific
properties of the implant reference is made to the sections above
directed to an implant according to the present invention
containing axitinib in an amount in the range from about 480 .mu.g
to about 750 .mu.g, or in an amount from about 560 .mu.g to about
660 .mu.g, or of about 600 .mu.g. The implant may be administered
into the vitreous humor, e.g. by means of a fine diameter, such as
a 25-gauge, needle. The treatment period as defined above may be at
least 4.5 months, or at least 6 months, or at least 9 months, or at
least 11 months, or at least 12 months, or at least 13 months, or
at least 14 months or even longer, such as up to about 15 months.
In particular embodiments, the treatment period is at least 6
months, or at least 9 months, or at least 12 months, or from about
6 to about 9 months.
[0349] In some embodiments concurrently with the treatment with the
sustained release biodegradable ocular implant(s) containing a TKI,
or a treatment with the sustained release biodegradable ocular
implant(s) containing axitinib according to the invention, an
anti-VEGF agent is administered to the patient. The anti-VEGF agent
may be selected from the group consisting of aflibercept,
bevacizumab, pegaptanib, ranibizumab, and brolucizumab. In certain
embodiments the anti-VEGF agent is bevacizumab. In particular
embodiments the anti-VEGF agent is aflibercept. In certain
embodiments the anti-VEGF agent is administered by means of an
intravitreal injection concurrently (as defined above) with the
administration of the sustained release biodegradable ocular
implant, optionally at the same time, i.e., in one session as
already disclosed above in detail. In cases where an administration
of the anti-VEGF agent and the implant of the present invention may
not be possible in the same session, e.g. due to administration
complications or patient-related reasons a successive
administration during two or more different sessions may
alternatively be applied, such as for instance administration of
two implants 7 days apart. This may still be considered as a
"concurrent" administration in the context of the present
invention.
[0350] In other embodiments, an anti-VEGF agent may be administered
in combination with an implant of the present invention, but not at
the same time (i.e., not concurrently), but at an earlier or a
later point during the treatment period of the implant of the
present invention. In certain embodiments, an anti-VEGF agent may
be administered within about 1, about 2, or about 3, or more months
of the administration of the implant, i.e., may be pre- or
post-administered as compared to the implant. This combined (and
planned) co-administration of an anti-VEGF agent differs from a
rescue medication as defined herein.
[0351] In certain embodiments of the present invention the patient
has a diagnosis of primary subfoveal (such as active sub- or
juxtafoveal CNV with leakage involving the fovea)
neovascularization (SFNV) secondary to AMD.
[0352] In certain embodiments of the present invention the patient
has a diagnosis of previously treated subfoveal neovascularization
(SFNV) secondary to neovascular AMD with leakage involving the
fovea. In such patient, the previous treatment was with an
anti-VEGF agent.
[0353] In some embodiments the patient is at least 50 or at least
60 years old. The patient may be male or female. The patient may
have retinal fluid such as intra-retinal fluid or sub-retinal
fluid.
[0354] In some embodiments the patient receiving the implant has a
history of an anti-VEGF treatment e.g. such as treatment with
LUCENTIS.RTM. and/or EYLEA.RTM.. In certain embodiments the patient
receiving the implant has a history of anti-VEGF treatment but has
not responded to this anti-VEGF treatment, i.e. the disease state
of the patient was not improved by the anti-VEGF treatment. In
embodiments where the patient has a history of an anti-VEGF
treatment before starting the treatment with the implant according
to the present invention, administration of the implant of the
present invention may prolong the effect of the prior anti-VEGF
treatment over an extended period of time, such as over the
treatment period defined above. In other embodiments the patient
receiving the implant has no history of an anti-VEGF treatment
(anti-VEGF naive, AMD treatment naive).
[0355] In certain embodiments the systemic plasma concentration of
the TKI such as axitinib is below 1 ng/mL, or below 0.5 ng/ml, or
below 0.3 ng/mL, or below 0.1 ng/mL (or below the limit of
quantification). As systemic concentrations of TKI are kept at a
minimum, the risk of drug-to-drug interactions or systemic toxicity
is also kept at a minimum. Therefore, in one embodiment additional
medication(s) taken by the patients do not provide a significant
risk. This is especially beneficial in older patients who are
frequently suffering from ocular diseases and are additionally
taking other medications.
[0356] Once injected the implants of certain embodiments of the
invention (comprising the hydrogel and the drug) biodegrade within
an extended period of time as disclosed above, e.g., about 9 to 12
months. In certain embodiments it may be that once the hydrogel is
fully degraded undissolved axitinib particles remain localized at
the site where the implant was located. These undissolved particles
may further maintain a rate of TKI delivery sufficient for
therapeutic effect (i.e. inhibition of vascular leakage) when the
hydrogel is degraded. FIG. 15 exemplarily presents the resorption
of the hydrogel and remaining axitinib particles at the former
implant location in one patient until 11 months after
administration. In certain embodiments, however, the entire amount
of TKI is dissolved prior to complete degradation of the
hydrogel.
[0357] In certain embodiments only mild or moderate adverse events
such as ocular adverse events are observed over the treatment
period. In certain embodiments no serious ocular adverse are
observed, and no treatment-related serious ocular adverse events
are observed. Tables 23 and 25 show the occurrence of adverse
events in the cohort 1 and 2, as well as the cohort 3a and 3b
subjects, respectively, of the clinical study the results of which
(as far as available) are presented in Example 6.4.
[0358] The invention in certain embodiments is further directed to
a method of reducing, essentially maintaining or preventing a
clinically significant increase of the central subfield thickness
as measured by optical coherence tomography in a patient whose
central subfield thickness is elevated due to an ocular disease
involving angiogenesis, the method comprising administering to the
patient the sustained release biodegradable ocular implant
containing a tyrosine kinase inhibitor of the present invention as
disclosed herein. In certain embodiments the ocular disease
involving angiogenesis is neovascular age-related macular
degeneration. In other embodiments the central subfield thickness
is reduced, essentially maintained or a clinically significant
increase of the central subfield thickness is prevented during a
period of at least 3 months, at least 4.5 months, at least 6
months, at least 9 months, at least 11 months, at least 12 months,
at least 13 months, or at least 14 months or even longer, such as
at least 15 months after administration to the patient whose
central subfield thickness is elevated due to an ocular disease
involving angiogenesis, such as neovascular age-related macular
degeneration. In certain embodiments, the patient's vision
expressed e.g. by the BCVA is not substantially impaired during the
treatment. In certain other embodiments, the patient's vision
expressed e.g. by the BCVA may even be improved. Accordingly, the
invention in certain embodiments is also directed to a method of
improving the vision of a patient whose vision is impaired e.g. due
to retinal fluid caused by an ocular disease involving
angiogenesis, wherein the method comprises administering an implant
according to the invention to the patient, such as by means of
intravitreal injection.
Additional Disclosure
[0359] In addition to the disclosure above, the present invention
also discloses the following items and lists of items:
First List of Items
[0360] 1. A sustained release biodegradable ocular implant
comprising a hydrogel and about 150 .mu.g to about 1200 .mu.g of a
tyrosine kinase inhibitor. [0361] 2. The sustained release
biodegradable ocular implant of item 1, wherein the tyrosine kinase
inhibitor is axitinib. [0362] 3. The sustained release
biodegradable ocular implant of claim 1 or 2, comprising the
tyrosine kinase inhibitor in an amount in the range from about 200
.mu.g to about 800 .mu.g. [0363] 4. The sustained release
biodegradable ocular implant of item 1 or 2, comprising the
tyrosine kinase inhibitor in an amount in the range from about 160
.mu.g to about 250 .mu.g. [0364] 5. The sustained release
biodegradable ocular implant of claim 4, comprising the tyrosine
kinase inhibitor in an amount in the range from about 180 .mu.g to
about 220 .mu.g. [0365] 6. The sustained release biodegradable
ocular implant of item 5, comprising the tyrosine kinase inhibitor
in an amount of about 200 .mu.g. [0366] 7. The sustained release
biodegradable ocular implant of claim 1 or 2, comprising the
tyrosine kinase inhibitor in an amount in the range from about 320
.mu.g to about 500 .mu.g. [0367] 8. The sustained release
biodegradable ocular implant of item 7, comprising the tyrosine
kinase inhibitor in an amount in the range from about 360 .mu.g to
about 440 .mu.g. [0368] 9. The sustained release biodegradable
ocular implant of claim 8, comprising the tyrosine kinase inhibitor
in an amount of about 400 .mu.g. [0369] 10. The sustained release
biodegradable ocular implant of item 1 or 2, comprising the
tyrosine kinase inhibitor in an amount in the range from about 480
.mu.g to about 750 .mu.g. [0370] 11. The sustained release
biodegradable ocular implant of claim 10, comprising the tyrosine
kinase inhibitor in an amount from about 540 .mu.g to about 660
.mu.g. [0371] 12. The sustained release biodegradable ocular
implant of item 11, comprising the tyrosine kinase inhibitor in an
amount of about 600 .mu.g. [0372] 13. The sustained release
biodegradable ocular implant of item 1 or 2, comprising the
tyrosine kinase inhibitor in an amount in the range from about 640
.mu.g to about 1000 .mu.g. [0373] 14. The sustained release
biodegradable ocular implant of item 13, comprising the tyrosine
kinase inhibitor in an amount from about 720 .mu.g to about 880
.mu.g. [0374] 15. The sustained release biodegradable ocular
implant of item 14, comprising the tyrosine kinase inhibitor in an
amount of about 800 .mu.g. [0375] 16. The sustained release
biodegradable ocular implant of any of the preceding items, wherein
the implant is for administration into the posterior section of the
eye. [0376] 17. The sustained release biodegradable ocular implant
of item 16, wherein the administration is into the vitreous humor.
[0377] 18. The sustained release biodegradable ocular implant of
any of the preceding items, wherein the tyrosine kinase inhibitor
particles are dispersed within the hydrogel. [0378] 19. The
sustained release biodegradable ocular implant of item 18, wherein
the tyrosine kinase inhibitor particles are micronized particles.
[0379] 20. The sustained release biodegradable ocular implant of
any of the preceding items, wherein the implant is in a dried state
prior to administration and becomes hydrated once administered into
the eye. [0380] 21. The sustained release biodegradable ocular
implant of any of the preceding items, wherein the hydrogel
comprises a polymer network comprising one or more units of
polyethylene glycol, polyethylene oxide, polypropylene oxide,
polyvinyl alcohol, poly (vinylpyrrolidinone), polylactic acid,
polylactic-co-glycolic acid, random or block copolymers or
combinations or mixtures of any of these, or one or more units of
polyaminoacids, glycosaminoglycans, polysaccharides, or proteins.
[0381] 22. The sustained release biodegradable ocular implant of
item 21, wherein the hydrogel comprises a polymer network that
comprises crosslinked polymer units that are identical or
different. [0382] 23. The sustained release biodegradable ocular
implant of item 22, wherein crosslinked polymer units are one or
more crosslinked polyethylene glycol units. [0383] 24. The
sustained release biodegradable ocular implant of any of items 21
to 23, wherein the polymer network comprises polyethylene glycol
units having an average molecular weight in the range from about
2,000 to about 100,000 Daltons. [0384] 25. The sustained release
biodegradable ocular implant of item 24, wherein the polyethylene
glycol units have an average molecular weight in the range from
about 10,000 to about 60,000 Daltons. [0385] 26. The sustained
release biodegradable ocular implant of item 25, wherein the
polyethylene glycol units have an average molecular weight in the
range from about 20,000 to about 40,000 Daltons. [0386] 27. The
sustained release biodegradable ocular implant of item 26, wherein
the polyethylene glycol units have an average molecular weight of
about 20,000 Daltons. [0387] 28. The sustained release
biodegradable ocular implant of any of items 21 to 27, wherein the
polymer network comprises one or more crosslinked multi-arm polymer
units. [0388] 29. The sustained release biodegradable ocular
implant of item 28, wherein the multi-arm polymer units comprise
one or more 2- to 10-arm polyethylene glycol units. [0389] 30. The
sustained release biodegradable ocular implant of item 29, wherein
the multi-arm polymer units comprise one or more 4- to 8-arm
polyethylene glycol units. [0390] 31. The sustained release
biodegradable ocular implant of item 30, wherein the multi-arm
polymer units comprise one or more 4-arm polyethylene glycol units.
[0391] 32. The sustained release biodegradable ocular implant of
any of items 21 to 31, wherein the polymer network comprises both
4-arm and 8-arm polyethylene glycol units. [0392] 33. The sustained
release biodegradable ocular implant of any of items 21 to 32,
wherein the polymer network is formed by reacting an electrophilic
group-containing multi-arm-polymer precursor with a nucleophilic
group-containing multi-arm polymer precursor. [0393] 34. The
sustained release biodegradable ocular implant of any of items 21
to 33, wherein the nucleophilic group is an amine group. [0394] 35.
The sustained release biodegradable ocular implant of any of items
21 to 34, wherein the electrophilic group is an activated ester
group. [0395] 36. The sustained release biodegradable ocular
implant of item 35, wherein the electrophilic group is an
N-hydroxysuccinimidyl (NHS) group. [0396] 37. The sustained release
biodegradable ocular implant of item 36, wherein the electrophilic
group is a succinimidylazelate (SAZ) group. [0397] 38. The
sustained release biodegradable ocular implant of any of items 32
to 37, wherein the 4-arm polyethylene glycol units are 4a20kPEG
units and the 8-arm polyethylene glycol units are 8a20kPEG units.
[0398] 39. The sustained release biodegradable ocular implant of
item 38, wherein the polymer network is obtained by reacting
4a20kPEG-SAZ with 8a20kPEG-NH.sub.2 in a weight ratio of about 2:1
or less. [0399] 40. The sustained release biodegradable ocular
implant of any of items 1 to 39, wherein the implant in a dried
state contains from about 25% to about 75% by weight of the
tyrosine kinase inhibitor and from about 20% to about 60% by weight
polymer units. [0400] 41. The sustained release biodegradable
ocular implant of item 40, wherein the implant in a dried state
contains from about 35% to about 65% by weight of the tyrosine
kinase inhibitor and from about 25% to about 50% by weight polymer
units. [0401] 42. The sustained release biodegradable ocular
implant of item 41, wherein the implant in a dried state contains
from about 45% to about 55% by weight of the tyrosine kinase
inhibitor and from about 37% to about 47% by weight polymer units.
[0402] 43. The sustained release biodegradable ocular implant of
any of the preceding items, wherein the implant contains one or
more phosphate, borate or carbonate salt(s). [0403] 44. The
sustained release biodegradable ocular implant of item 43, wherein
the implant contains phosphate salt originating from phosphate
buffer used during the preparation of the hydrogel. [0404] 45. The
sustained release biodegradable ocular implant of any of the
preceding items, wherein the hydrogel in a wet state contains about
3% to about 20% polyethylene glycol representing the polyethylene
glycol weight divided by the fluid weight.times.100. [0405] 46. The
sustained release biodegradable ocular implant of item 45, wherein
the hydrogel contains about 7.5% to about 15% polyethylene glycol
representing the polyethylene glycol weight divided by the fluid
weight.times.100. [0406] 47. The sustained release biodegradable
ocular implant of any of the preceding items, wherein the implant
in a dried state contains not more than about 1% by weight water.
[0407] 48. The sustained release biodegradable ocular implant of
any of the preceding items, wherein the implant has an essentially
cylindrical shape or another shape such as a cross shape. [0408]
49. The sustained release biodegradable ocular implant of any of
the preceding items, wherein the implant is in the form of a fiber.
[0409] 50. The sustained release biodegradable ocular implant of
any of the preceding items, wherein the implant is administered to
the eye through a needle. [0410] 51. The sustained release
biodegradable ocular implant of item 50, wherein the needle is a
25- or 27-gauge needle. [0411] 52. The sustained release
biodegradable ocular implant of any of the preceding items, wherein
upon hydration in vivo in the eye or in vitro the diameter of the
implant is increased, or the length of the implant is decreased
while its diameter is increased. [0412] 53. The sustained release
biodegradable ocular implant of item 52, wherein hydration is
measured in vitro in phosphate-buffered saline at a pH of 7.2 at
37.degree. C. after 24 hours. [0413] 54. The sustained release
biodegradable ocular implant of any of items 17 to 53, wherein the
implant biodegrades in the vitreous humor within about 2 to about
15 months after administration. [0414] 55. The sustained release
biodegradable ocular implant of item 54, wherein the implant
biodegrades in the vitreous humor within about 4 to about 13 months
after administration. [0415] 56. The sustained release
biodegradable ocular implant of item 55, wherein the implant
biodegrades in the vitreous humor within about 9 to about 12 months
after administration. [0416] 57. The sustained release
biodegradable ocular implant of any of items 2 to 56, wherein the
implant after administration to the vitreous humor releases a
therapeutically effective amount of axitinib over a period of at
least about 3 months, at least about 6 months, at least about 9
months, at least about 10 months, at least about 11 months, at
least about 12 months, at least about 13 months, or at least about
14 months after administration. [0417] 58. The sustained release
biodegradable ocular implant of item 57, wherein the implant after
administration to the vitreous humor releases a therapeutically
effective amount of axitinib over a period of at least about 6
months. [0418] 59. The sustained release biodegradable ocular
implant of item 57, wherein the implant after administration to the
vitreous humor releases a therapeutically effective amount of
axitinib over a period of at least about 9 months. [0419] 60. The
sustained release biodegradable ocular implant of any of items 17
to 59, wherein axitinib is released from the implant after
administration at an average rate of about 0.1 .mu.g/day to about
10 .mu.g/day. [0420] 61. The sustained release biodegradable ocular
implant of item 60, wherein axitinib is released from the implant
at an average rate of about 0.5 .mu.g/day to about 7 .mu.g/day.
[0421] 62. The sustained release biodegradable ocular implant of
item 61, wherein axitinib is released from the implant at an
average rate about 1 .mu.g/day to about 5 .mu.g/day. [0422] 63. The
sustained release biodegradable ocular implant of any of items 17
to 62, wherein the implant biodegrades in the vitreous humor prior
to complete solubilization of the tyrosine kinase inhibitor
particles contained in the implant. [0423] 64. The sustained
release biodegradable ocular implant of any of items 17 to 63,
wherein the entire amount of the tyrosine kinase inhibitor
contained in the implant is released prior to the complete
degradation of the implant in the vitreous humor. [0424] 65. The
sustained release biodegradable ocular implant of any of the
preceding items, wherein the implant is obtainable by preparing a
mixture containing hydrogel precursors and a tyrosine kinase
inhibitor, filling the mixture into a tubing, allowing the hydrogel
to gel in the tubing to provide a hydrogel shaped as a fiber, and
stretching the hydrogel fiber. [0425] 66. The sustained release
biodegradable ocular implant of item 65, wherein the fiber has been
stretched and/or twisted prior to or after drying. [0426] 67. The
sustained release biodegradable ocular implant of item 66, wherein
the fiber has been stretched by a stretch factor in the
longitudinal direction of from about 1.0 to about 4.5. [0427] 68. A
sustained release biodegradable ocular implant containing axitinib
in an amount of 160 .mu.g to about 250 .mu.g, or from about 180
.mu.g to about 220 .mu.g, or about 200 .mu.g dispersed in a
hydrogel, wherein the hydrogel comprises a polymer network
comprising polyethylene glycol units, and wherein the implant is in
a dried state prior to administration. [0428] 69. The sustained
release biodegradable ocular implant of item 68, wherein the
polymer network is formed by reacting 4a20kPEG-SAZ with
8a20kPEG-NH.sub.2. [0429] 70. The sustained release biodegradable
ocular implant of item 69, wherein the hydrogel when formed and
before being dried contains 7.5% polyethylene glycol, representing
the polyethylene glycol weight divided by the fluid
weight.times.100. [0430] 71. The sustained release biodegradable
ocular implant of any of items 68 to 70, wherein the implant in a
dried state contains from about 45% to about 55% by weight axitinib
and from about 37% to about 47% by weight polyethylene glycol
units. [0431] 72. The sustained release biodegradable ocular
implant of any of items 68 to 71, wherein the implant in a dried
state contains not more than about 1% by weight water. [0432] 73.
The sustained release biodegradable ocular implant of any of items
68 to 72, wherein the polymer network is formed by reacting
4a20kPEG-SAZ with 8a20kPEG-NH.sub.2 in a weight ratio of about 2:1
or less. [0433] 74. The sustained release biodegradable ocular
implant of any of items 68 to 73, wherein the implant releases in
vitro about 0.01 .mu.g to about 0.15 .mu.g of axitinib per day in
phosphate-buffered saline at 37.degree. C. for a period of 30 days.
[0434] 75. The sustained release biodegradable ocular implant of
any of items 68 to 74, wherein the implant releases in vitro about
35% to about 45% of the axitinib in 3 days, about 65% to about 75%
of the axitinib in 7 days, and about 90% to about 100% of the
axitinib in 12 to 13 days in a 25:75 ethanol/water mixture (v/v) at
37
.degree. C. [0435] 76. The sustained release biodegradable ocular
implant of any of items 68 to 75, wherein the implant releases in
vitro about 25% to about 35% of the axitinib in 2 months, about 47%
to about 57% of the axitinib in 3 months, about 70% to about 80% of
the axitinib in 5 months, and about 90% to about 100% of the
axitinib in 7 months in phosphate buffered saline at a pH of 7.2,
at 37.degree. C. and with an octanol top layer. [0436] 77. The
sustained release biodegradable ocular implant of any of items 68
to 76, wherein the implant is in the form of a fiber that has an
average length of about 15 mm to about 16.5 mm and an average
diameter of about 0.20 mm to about 0.30 mm in its dried state.
[0437] 78. The sustained release biodegradable ocular implant of
item 77, which decreases in length and increases in diameter upon
hydration in vivo in the eye or in vitro, wherein hydration in
vitro is measured in phosphate-buffered saline at a pH of 7.2 at
37.degree. C. after 24 hours. [0438] 79. The sustained release
biodegradable ocular implant of item 77 or 78, wherein the implant
in its hydrated state has an average length of about 6.5 to about 8
mm and an average diameter of about 0.70 to about 0.80 mm. [0439]
80. The sustained release biodegradable ocular implant of any of
items 68 to 79, wherein the implant is obtainable by preparing a
mixture containing hydrogel precursors and axitinib, filling the
mixture into a tubing, allowing the hydrogel to gel in the tubing
to provide a hydrogel shaped as a fiber, and stretching the
hydrogel fiber. [0440] 81. The sustained release biodegradable
ocular implant of item 80, wherein the fiber is stretched after
drying by a factor of about 2 to about 5. [0441] 82. The sustained
release biodegradable ocular implant of item 81, wherein the fiber
is stretched after drying by a factor of about 3 to about 4.5.
[0442] 83. The sustained release biodegradable ocular implant of
any of items 68 to 82, wherein the implant in a dried state is
loaded in a needle, such as a 25-gauge needle or a 27-gauge needle,
for injection into the vitreous humor. [0443] 84. A sustained
release biodegradable ocular implant containing axitinib in an
amount in the range from about 480 .mu.g to about 750 .mu.g
dispersed in a hydrogel, wherein the hydrogel comprises a polymer
network. [0444] 85. The sustained release biodegradable ocular
implant of item 84, wherein the polymer network comprises
crosslinked polyethylene glycol units. [0445] 86. The sustained
release biodegradable ocular implant of item 85, wherein the
axitinib is contained in an amount in the range from about 540
.mu.g to about 660 .mu.g. [0446] 87. The sustained release
biodegradable ocular implant of item 86, wherein the axitinib is
contained in an amount of about 600 .mu.g. [0447] 88. The sustained
release biodegradable ocular implant of any of items 84 to 87,
wherein the polyethylene glycol units comprise 4-arm and/or 8-arm
polyethylene glycol units having an average molecular weight in the
range from about 10,000 Daltons to about 60,000 Daltons. [0448] 89.
The sustained release biodegradable ocular implant of item 88,
wherein the polyethylene glycol units comprise 4a20kPEG units.
[0449] 90. The sustained release biodegradable ocular implant of
item 89, wherein the polymer network is formed by reacting
4a20kPEG-SAZ with 8a20kPEG-NH.sub.2. [0450] 91. The sustained
release biodegradable ocular implant of item 90, wherein the weight
ratio of 4a20kPEG-SAZ to 8a20kPEG-NH.sub.2 is about 2:1 or less.
[0451] 92. The sustained release biodegradable ocular implant of
any of items 84 to 91, wherein the implant in a dried state
contains from about 45% to about 55% by weight axitinib and from
about 37% to about 47% by weight polyethylene glycol units. [0452]
93. The sustained release biodegradable ocular implant of any of
items 84 to 92, wherein the implant in a dried state contains not
more than about 1% by weight water. [0453] 94. The sustained
release biodegradable ocular implant of any of items 84 to 93,
wherein the implant is in the form of a fiber that in its dried
state has an average length of about 7 mm to about 12 mm and an
average diameter of about 0.25 mm to about 0.50 mm. [0454] 95. The
sustained release biodegradable ocular implant of item 94, wherein
the implant is in the form of a fiber that in its dried state has
an average length of about 8 mm to about 11 mm and an average
diameter of about 0.3 mm to about 0.4 mm. [0455] 96. The sustained
release biodegradable ocular implant of any of items 84 to 95,
wherein the implant is for administration to the vitreous humor.
[0456] 97. The sustained release biodegradable ocular implant of
item 94 to 96, which increases in diameter upon hydration in vivo
in the eye or in vitro, wherein hydration in vitro is measured in
phosphate-buffered saline at a pH of 7.2 at 37.degree. C. after 24
hours. [0457] 98. The sustained release biodegradable ocular
implant of item 97, wherein the implant in its hydrated state has
an average length of about 9 mm to about 12 mm and an average
diameter of about 0.5 mm to about 0.8 mm. [0458] 99. The sustained
release biodegradable ocular implant of item 98, wherein the
implant in its hydrated state has an average length of about 9.5 mm
to about 11.5 mm and an average diameter of about 0.65 mm to about
0.75 mm, or has an average length in its hydrated state of not more
than about 10 mm or not more than about 9 mm. [0459] 100. The
sustained release biodegradable ocular implant of any of items 84
to 99, wherein the implant contains about 600 .mu.g axitinib and
releases in vitro about 0.3 .mu.g to about 0.5 .mu.g of axitinib
per day in phosphate-buffered saline at 37.degree. C. for a period
of 30 days. [0460] 101. The sustained release biodegradable ocular
implant of any one of items 84 to 100, wherein the implant releases
in vitro about 40% to about 60% of the axitinib in 2 days, about
65% to about 85% of the axitinib in 4 days, and about 75% to about
90% of the axitinib in 6 days in a 25:75 ethanol/water mixture
(v/v) at 37.degree. C. [0461] 102. The sustained release
biodegradable ocular implant of item 101, wherein the implant
releases in vitro about 45% to about 55% of the axitinib in 2 days,
about 70% to about 80% of the axitinib in 4 days, and about 80% to
about 90% of the axitinib in 6 days in a 25:75 ethanol/water
mixture (v/v) at 37.degree. C. [0462] 103. The sustained release
biodegradable ocular implant of any of items 84 to 102, wherein the
implant is obtainable by preparing a mixture containing hydrogel
precursors and axitinib, filling the mixture into a tubing,
allowing the hydrogel to gel in the tubing to provide a hydrogel
shaped as a fiber, and stretching the hydrogel fiber. [0463] 104.
The sustained release biodegradable ocular implant of item 103,
wherein the fiber is wet-stretched prior to drying by a factor of
about 0.5 to about 5. [0464] 105. The sustained release
biodegradable ocular implant of item 104, wherein the fiber is
wet-stretched prior to drying by a factor of about 1 to about 4.
[0465] 106. The sustained release biodegradable ocular implant of
item 105, wherein the fiber is wet-stretched prior to drying by a
factor of about 1.5 to about 3.5. [0466] 107. The sustained release
biodegradable ocular implant of item 106, wherein the fiber is
wet-stretched prior to drying by a factor of about 1.7 to about 3.
[0467] 108. The sustained release biodegradable ocular implant of
any of items 84 to 107, wherein the implant in a dried state is
loaded in a needle for injection into the vitreous humor. [0468]
109. The sustained release biodegradable ocular implant of item
108, wherein the implant in a dried state is loaded in a 25-gauge
or a 27-gauge needle. [0469] 110. The sustained release
biodegradable ocular implant of any of items 1 to 109, wherein the
hydrogel comprises a polymer network which is semi-crystalline in
the dry state at or below room temperature, and amorphous in the
wet state. [0470] 111. The sustained release biodegradable ocular
implant of any of items 1 to 110, wherein the implant has undergone
wet or dry stretching during manufacture, and wherein the implant
in the stretched form is dimensionally stable when in the dry state
at or below room temperature. [0471] 112. A method of treating an
ocular disease in a patient in need thereof, the method comprising
administering to the patient a sustained release biodegradable
ocular implant comprising a hydrogel and a tyrosine kinase
inhibitor according to any of the preceding items, wherein the dose
per eye administered once for a treatment period of at least 3
months is from about 150 .mu.g to about 1200 .mu.g of the tyrosine
kinase inhibitor. [0472] 113. The method of item 112, wherein the
tyrosine kinase inhibitor is axitinib. [0473] 114. The method of
item 112 or 113, wherein the dose administered per eye once for the
treatment period is in the range from about 200 .mu.g to about 800
.mu.g. [0474] 115. The method of item 112 or 113, wherein the dose
is in the range from about 160 .mu.g to about 250 .mu.g, or from
about 180 .mu.g to about 220 .mu.g. [0475] 116. The method of item
115, wherein the dose is about 200 .mu.g. [0476] 117. The method of
item 112 or 113, wherein the dose is in the range from about 320
.mu.g to about 500 .mu.g, or from about 360 .mu.g to about 440
.mu.g. [0477] 118. The method of item 117, wherein the dose is
about 400 .mu.g. [0478] 119. The method of item 112 or 113, wherein
the dose is in the range from about 480 .mu.g to about 750 .mu.g,
or from about 540 .mu.g to about 660 .mu.g. [0479] 120. The method
of item 119, wherein the dose is about 600 .mu.g. [0480] 121. The
method of item 112 or 113, wherein the dose is in the range from
about 640 .mu.g to about 1000 .mu.g, or from about 720 .mu.g to
about 880 .mu.g. [0481] 122. The method of item 121, wherein the
dose is about 800 .mu.g. [0482] 123. The method of any of items 112
to 122, wherein the ocular disease involves angiogenesis. [0483]
124. The method of any of items 112 to 123, wherein the ocular
disease is mediated by one or more receptor tyrosine kinases
(RTKs), specifically VEGFR-1, VEGFR-2, VEGFR-3,
PDGFR-.alpha./.beta., and/or c-Kit. [0484] 125. The method of any
of items 112 to 124, wherein the ocular disease is a retinal
disease including Choroidal Neovascularization, Diabetic
Retinopathy, Diabetic Macular Edema, Retinal Vein Occlusion, Acute
Macular Neuroretinopathy, Central Serous Chorioretinopathy, and
Cystoid Macular Edema; wherein the ocular disease is Acute
Multifocal Placoid Pigment Epitheliopathy, Behcet's Disease,
Birdshot Retinochoroidopathy, Infectious (Syphilis, Lyme,
Tuberculosis, Toxoplasmosis), Intermediate Uveitis (Pars Planitis),
Multifocal Choroiditis, Multiple Evanescent White Dot Syndrome
(MEWDS), Ocular Sarcoidosis, Posterior Scleritis, Serpignous
Choroiditis, Subretinal Fibrosis, Uveitis Syndrome, or
Vogt-Koyanagi-Harada Syndrome; wherein the ocular disease is a
vascular disease or exudative diseases, including Coat's Disease,
Parafoveal Telangiectasis, Papillophlebitis, Frosted Branch
Angitis, Sickle Cell Retinopathy and other Hemoglobinopathies,
Angioid Streaks, and Familial Exudative Vitreoretinopathy; or
wherein the ocular disease results from trauma or surgery,
including Sympathetic Ophthalmia, Uveitic Retinal Disease, Retinal
Detachment, Trauma, Photodynamic Laser Treatment, Photocoagulation,
Hypoperfusion During Surgery, Radiation Retinopathy, or Bone Marrow
Transplant Retinopathy. [0485] 126. The method of any of items 112
to 124, wherein the ocular disease is neovascular age-related
macular degeneration, diabetic macular edema or retinal vein
occlusion. [0486] 127. The method of item 126, wherein the disease
is neovascular age-related macular degeneration. [0487] 128. The
method of any of items 112 to 127, wherein the treatment is
effective in reducing, essentially maintaining or preventing a
clinically significant increase ofthe central subfield thickness as
measured by optical coherence tomography in a patient whose central
subfield thickness is elevated. [0488] 129. The method of any of
items 112 to 128, wherein the dose per eye administered once for
the treatment period is contained in one implant or in two, three
or more implants administered concurrently. [0489] 130. The method
of any of items 112 to 129, wherein the implant is administered by
injection into the vitreous humor. [0490] 131. The method of any of
items 112 to 130, wherein the treatment period is at least 3 about
months, at least about 4.5 months, at least about 6 months, at
least about 9 months, at least about 11 months, at least about 12
months, at least about 13 months, or at least about 14 months.
[0491] 132. The method of item 131, wherein the treatment period is
at least 6 months, at least about 9 months, or at least about 12
months. [0492] 133. The method of any of items 112 to 132, wherein
concurrently with the treatment with the sustained release ocular
implant an anti-VEGF agent is administered to the patient, or
wherein an anti-VEGF agent is administered within about 1, about 2
or about 3 months from the administration of the implant. [0493]
134. The method of item 133, wherein the anti-VEGF agent is
selected from the group consisting of aflibercept, bevacizumab,
pegaptanib, ranibizumab, and brolucizumab. [0494] 135. The method
of item 134, wherein the anti-VEGF agent is bevacizumab. [0495]
136. The method of any of items 133 to 135, wherein the anti-VEGF
agent is administered by means of intravitreal injection. [0496]
137. The method of any of items 112 to 136, wherein the patient
receiving the implant has a history of an anti-VEGF treatment.
[0497] 138. The method of any of items 112 to 136, wherein the
patient receiving the implant has no history of an anti-VEGF
treatment (anti-VEGF naive). [0498] 139. A method of treating
neovascular age-related macular degeneration in a patient in need
thereof, the method comprising administering to the patient a
sustained release biodegradable ocular implant comprising a
hydrogel that comprises a polymer network and about 200 .mu.g of a
tyrosine kinase inhibitor, wherein one implant per eye is
administered once for a treatment period of at least 9 months, and
wherein the patient has a history of an anti-VEGF treatment. [0499]
140. A method of treating neovascular age-related macular
degeneration in a patient in need thereof, the method comprising
administering to the patient a sustained release biodegradable
ocular implant comprising a hydrogel that comprises a polymer
network and about 200 .mu.g of a tyrosine kinase inhibitor, wherein
two implants per eye forming a total dose of about 400 .mu.g are
administered once for a treatment period of at least 3 months, and
wherein the patient has a history or has no history of an anti-VEGF
treatment. [0500] 141. The method of item 139 or 140, wherein the
treatment results in a reduction in central subfield thickness
(CSFT) as measured by optical coherence tomography during the
treatment period.
[0501] 142. The method of any of items 139 to 141, wherein the
tyrosine kinase inhibitor is axitinib and is dispersed in the
hydrogel which comprises a polymer network formed by reacting
4a20kPEG-SAZ with 8a20kPEG-NH.sub.2, and wherein the implant is in
a dried state prior to administration. [0502] 143. The method of
item 142, wherein the hydrogel when formed and before being dried
contains about 7.5% polyethylene glycol, representing the
polyethylene glycol weight divided by the fluid weight.times.100.
[0503] 144. The method of any of items 140 to 143 wherein the
treatment period is at least 9 months. [0504] 145. A method of
treating neovascular age-related macular degeneration in a patient
in need thereof, the method comprising administering to the patient
a sustained release biodegradable ocular implant comprising
axitinib in an amount in the range from about 480 .mu.g to about
750 .mu.g dispersed in a hydrogel comprising a polymer network,
wherein the implant is administered once for a treatment period of
at least 3 months. [0505] 146. The method of item 145, wherein the
axitinib is contained in the implant in an amount from about 560
.mu.g to about 660 .mu.g, [0506] 147. The method of item 146,
wherein the axitinib is contained in the implant in an amount of
about 600 .mu.g. [0507] 148. The method of any of items 145 to 147,
wherein the implant is as defined in items 84 to 111. 149. The
method of any of items 145 to 148, wherein the implant is
administered into the vitreous humor. [0508] 150. The method of any
of items 145 to 149, wherein the treatment period is at least about
3 months, at least about 6 months, at least about 9 months, at
least about 11 months, at least about 12 months, at least about 13
months, or at least about 14 months. [0509] 151. The method any of
items 145 to 150, wherein the implant is administered by injection
into the vitreous humor by means of a 25- or a 27-gauge needle.
[0510] 152. The method of any of items 145 to 151, wherein the
patient receiving the implant has a history of an anti-VEGF
treatment, or has no history of an anti-VEGF treatment (anti-VEGF
naive). [0511] 153. The method of any of items 145 to 152, wherein
an anti-VEGF agent is administered to the patient concurrently with
the implant. [0512] 154. The method of item 153, wherein the
anti-VEGF agent is selected from the group consisting of
aflibercept, bevacizumab, pegaptanib, ranibizumab, and
brolucizumab. [0513] 155. The method of item 154, wherein the
anti-VEGF agent is bevacizumab. [0514] 156. The method of any of
items 153 to 155, wherein the anti-VEGF agent is administered by
means of intravitreal injection. [0515] 157. The method of any of
items 112 to 156, wherein the number of adverse events during the
administration of the sustained release biodegradable ocular
implant is low. [0516] 158. The method of item 157, wherein the
number of treatment-related ocular adverse events during the
administration of the sustained release biodegradable ocular
implant is low. [0517] 159. A method of manufacturing a sustained
release biodegradable ocular implant comprising a hydrogel and
about 150 .mu.g to about 1200 .mu.g of a tyrosine kinase inhibitor
according to any of items 1 to 111, the method comprising the steps
of forming a hydrogel comprising a polymer network and tyrosine
kinase inhibitor particles dispersed in the hydrogel, shaping the
hydrogel and drying the hydrogel. [0518] 160. The method of item
159, wherein the tyrosine kinase inhibitor is axitinib. [0519] 161.
The method of item 159 or 160, wherein the tyrosine kinase
inhibitor particles are micronized and/or homogeneously dispersed
within the hydrogel. [0520] 162. The method of any of items 159 to
161, wherein the polymer network is formed by crosslinking
multi-arm polyethylene glycol units in a buffered solution. [0521]
163. The method of any of items 159 to 162, wherein the hydrogel
comprises a polymer network that is formed by mixing and reacting
an electrophilic group-containing multi-arm polyethylene glycol
with a nucleophilic group-containing multi-arm polyethylene glycol
in a buffered solution in the presence of the tyrosine kinase
inhibitor, and allowing the mixture to gel. [0522] 164. The method
of item 163, comprising reacting 4a20kPEG-SAZ with
8a20kPEG-NH.sub.2 in a weight ratio of about 2:1. [0523] 165. The
method of item 163 or 164, wherein the method comprises the steps
of filling the mixture into a mold or tubing prior to complete
gelling in order to provide the desired final shape of the
hydrogel, allowing the mixture to gel, and drying the hydrogel.
[0524] 166. The method of item 165, wherein the mixture is filled
into a fine diameter tubing in order to prepare a hydrogel fiber.
[0525] 167. The method of item 166, wherein the inside of the
tubing has a round geometry. [0526] 168. The method of item 166,
wherein the inside of the tubing has a non-round geometry. [0527]
169. The method of item 168, wherein the inside of the tubing has a
cross-shaped geometry. [0528] 170. The method of any of items 166
to 169, wherein the method further comprises stretching the fiber
and/or twisting the fiber. [0529] 171. The method of item 170,
wherein the stretching is performed prior to or after drying the
hydrogel. [0530] 172. The method of item 171, wherein the fiber is
stretched by a stretch factor of about 1 to about 4.5. [0531] 173.
The method of item 171, wherein the implant contains axitinib in an
amount of about 200 .mu.g and the stretching is performed after
drying the hydrogel by a stretch factor of about 2 to about 5 or a
stretch factor of about 3 to about 4.5. [0532] 174. The method of
item 171, wherein the implant contains axitinib in an amount of
about 600 .mu.g and the stretching is performed in a wet state
prior to drying the hydrogel at a stretch factor of about 0.5 to
about 5, or a stretch factor of about 1 to about 4, or a stretch
factor of about 1.3 to about 3.5, or a stretch factor of about 1.7
to about 3. [0533] 175. The method of any of items 159 to 174,
wherein the method further comprises loading the implant in a dried
state into a needle. [0534] 176. The method of item 175, wherein
the needle is a 25- or 27-gauge needle. [0535] 177. A method of
imparting shape memory to a hydrogel fiber comprising an active
agent dispersed in the hydrogel by stretching the hydrogel fiber in
the longitudinal direction. [0536] 178. A method of manufacturing
an ocular implant comprising a hydrogel comprising an active agent
dispersed therein, wherein the implant changes its dimensions upon
administration to the eye, the method comprising preparing a fiber
of the hydrogel and stretching the fiber in the longitudinal
direction. [0537] 179. The method of item 177 or 178, wherein the
method comprises the step of drying the hydrogel, wherein the fiber
is stretched in the longitudinal direction prior to or after said
drying (wet or dry stretching). [0538] 180. The method of any of
items 177 to 179, wherein the fiber is stretched by a factor of
about 0.5 to about 5, or a factor of about 1 to about 4.5, or a
factor of about 3 to about 4.5 or a factor of about 1 to about 2.
[0539] 181. The method of any of items 177 to 180, wherein the
active agent is a tyrosine kinase inhibitor, such as axitinib.
[0540] 182. The method of any of items 177 to 181, wherein the
hydrogel comprises a polymer network comprising crosslinked
polyethylene glycol units. [0541] 183. The method of any of items
177 to 182, wherein the fiber upon hydration fully or partly
returns to approximately its original length and/or original
diameter that it had prior to the stretching. [0542] 184. The
method of any of items 177 to 183, wherein the change in dimensions
is an increase in diameter, or an increase in diameter together
with a decrease in length. [0543] 185. A kit comprising one or more
sustained release biodegradable ocular implant(s) according to any
of items 1 to 111 or manufactured in accordance with the method of
any of items 159 to 176 and one or more needle(s), wherein the one
or more needle(s) is/are each pre-loaded with one sustained release
biodegradable ocular implant in a dried state. [0544] 186. The kit
of item 185, wherein the needle(s) is/are 25- or 27-gauge
needle(s). [0545] 187. The kit of item 185 or 186, wherein the kit
comprises one or more 25- or 27-gauge needle(s) each loaded with an
implant containing axitinib in an amount in the range from about
180 .mu.g to about 220 .mu.g. [0546] 188. The kit of item 187,
wherein the implant contains axitinib in an amount of about 200
.mu.g. [0547] 189. The kit of item 185 or 186, wherein the kit
comprises one 25-gauge or 27-gauge needle loaded with an implant
containing axitinib in an amount in the range from about 540 .mu.g
to about 660 .mu.g. [0548] 190. The kit of item 189, wherein the
implant contains axitinib in an amount of about 600 .mu.g. [0549]
191. The kit of any of items 185 to 190, further containing an
injection device for injecting the implant into the eye of a
patient. [0550] 192. The kit of item 191, wherein the injection
device is provided in the kit separately from the one or more
needle(s) loaded with implant. [0551] 193. The kit of item 191,
wherein the injection device is pre-connected to a needle loaded
with implant. [0552] 194. The kit of item 191 or 192, wherein the
injection device contains a push wire to deploy the implant from
the needle into the eye. [0553] 195. The kit of any of items 185 to
194, further comprising one dose of an anti-VEGF agent ready for
injection. [0554] 196. An injection device suitable for injecting a
sustained release biodegradable ocular implant according to any of
items 1 to 111 into the eye. [0555] 197. The injection device of
item 196 containing means for connecting the injection device to a
needle, [0556] 198. The injection device of item 196 or 197,
wherein the needle is pre-loaded with the implant. [0557] 199. The
injection device of any of items 196 to 198 containing a push wire
to deploy the implant from the needle into the eye when the
injection device has been connected to the needle. [0558] 200. The
injection device of item 199, wherein the push wire is made of
Nitinol or stainless steel/Teflon. [0559] 201. The injection device
of item 199 or 200, obtainable by affixing the wire to the plunger
and encasing it between two snap fit injector body parts and
securing the plunger with a clip. [0560] 202. A pharmaceutical
product comprising the sustained release biodegradable ocular
implant of any of items 1 to 111 loaded in a needle and an
injection device according to any of items 196 to 201, wherein the
needle is pre-connected to the injection device. [0561] 203. A
sustained release biodegradable ocular implant containing a
tyrosine kinase inhibitor according to any of items 1 to 111 for
use in treating an ocular disease in a patient in need thereof
according to any of items 112 to 138 or in treating neovascular
age-related macular degeneration in a patient in need thereof
according to any of items 139 to 158, 210 or 211. [0562] 204. Use
of a sustained release biodegradable ocular implant containing a
tyrosine kinase inhibitor according to any of items 1 to 111 in the
preparation of a medicament for the treatment of an ocular disease
in a patient in need thereof according to any of items 112 to 138
or for the treatment of neovascular age-related macular
degeneration in a patient in need thereof according to any of items
139 to 158, 210 or 211. [0563] 205. A method of reducing,
essentially maintaining or preventing a clinically significant
increase of the central subfield thickness as measured by optical
coherence tomography in a patient whose central subfield thickness
is elevated due to an ocular disease involving angiogenesis, the
method comprising administering to the patient the sustained
release biodegradable ocular implant containing a tyrosine kinase
inhibitor according to any of items 1 to 111. [0564] 206. The
method of item 205, wherein the ocular disease is neovascular
age-related macular degeneration. [0565] 207. The method of item
205 or 206, wherein the central subfield thickness is reduced,
essentially maintained or a clinically significant increase of the
central subfield thickness is prevented in the patient during a
period of at least about 3 months, at least about 6 months, at
least about 9 months, at least about 11 months, at least about 12
months, at least about 13 months, or at least about 14 months after
administration of the implant with respect to a baseline central
subfield thickness measured in that patient prior to the
administration of the implant. [0566] 208. A sustained release
biodegradable ocular implant containing a tyrosine kinase inhibitor
according to any of items 1 to 111 for use in reducing, essentially
maintaining or preventing a clinically significant increase of the
central subfield thickness as measured by optical coherence
tomography in a patient whose central subfield thickness is
elevated due to an ocular disease involving angiogenesis according
to any of items 205 to 207, 210 or 211. [0567] 209. Use of a
sustained release biodegradable ocular implant containing a
tyrosine kinase inhibitor according to any of items 1 to 111 in the
preparation of a medicament for reducing, essentially maintaining
or preventing a clinically significant increase in the central
subfield thickness as measured by optical coherence tomography in a
patient whose central subfield thickness is elevated due to an
ocular disease involving angiogenesis according to any of items 205
to 207, 210 or 211. [0568] 210. The method of any of items 128 to
158 or any of items 205 to 207, wherein the patient's vision
expressed by means of the best corrected visual acuity is not
impaired, or is improved. [0569] 211. The method of any of items
128 to 158, any of items 205 to 207 or item 210, wherein rescue
medication is not required to be administered during the treatment
period, or wherein rescue medication is only required to be
administered rarely, such as 1, 2 or 3 times, during the treatment
period. [0570] 212. The method of item 211, wherein the duration of
the treatment period is from about 6 to about 9 months after
administration of the sustained release biodegradable ocular
implant. [0571] 213. A method of improving the vision of a patient
whose vision is impaired due to an ocular disease involving
angiogenesis, the method comprising administering to the patient
the sustained release biodegradable ocular implant containing a
tyrosine kinase inhibitor according to any of items 1 to 111.
[0572] 214. The method of item 213, wherein the ocular disease is
neovascular age-related macular degeneration, diabetic macular
edema or retinal vein occlusion. [0573] 215. The method of item 213
or item 214, wherein the patient's vision is impaired due to the
presence of retinal fluid. [0574] 216. The method of any of items
213 to 215, wherein the improvement of vision is manifested by
means of an increase in best corrected visual acuity.
[0575] 217. The method of item 216, wherein the best corrected
visual acuity is increased by at least 10, at least 15, or at least
20 ETDRS letters. [0576] 218. A sustained release biodegradable
ocular implant containing a tyrosine kinase inhibitor according to
any of items 1 to 111 for use in improving the vision of a patient
whose vision is impaired due to an ocular disease involving
angiogenesis according to the method of any of items 213 to 217.
[0577] 219. Use of a sustained release biodegradable ocular implant
containing a tyrosine kinase inhibitor according to any of items 1
to 111 in the preparation of a medicament for improving the vision
of a patient whose vision is impaired due to an ocular disease
involving angiogenesis according to the method of any of items 213
to 217.
Second List of Items
[0578] 1. A sustained-release biodegradable ocular hydrogel implant
comprising a tyrosine kinase inhibitor, a polymer network, and a
clearance zone, wherein the clearance zone is devoid of the TKI
prior to release of the TKI. 2. The ocular hydrogel of item 1,
wherein the TKI is not in contact with retinal cells when the TKI
is comprised inside the hydrogel implant. 3. The ocular hydrogel of
item 1 or 2, wherein the TKI is present in the hydrogel implant at
or near its saturation level. 4. The ocular hydrogel implant of any
one of items 1 to 3, wherein the size of the clearance zone
increases as a function of the amount of TKI release. 5. The ocular
hydrogel implant of any one of items 1 to 4, wherein the ocular
hydrogel implant is fully degraded following release of the TKI or
following release of at least 90% of the TKI. 6. The ocular
hydrogel implant of any one of items 1 to 5, wherein the ocular
hydrogel implant is fully degraded after about 30 days or after
about 3 months following complete release of the TKI. 7. The ocular
hydrogel implant of any one of items 1 to 4, wherein degradation of
the ocular hydrogel occurs prior to release of the TKI. 8. The
ocular hydrogel implant of any one of items 1 to 7, wherein the
polymer network comprises a plurality of polyethylene glycol (PEG)
units. 9. The ocular hydrogel implant of any one of items 1 to 8,
wherein the polymer network comprises a plurality of multi-arm PEG
units. 10. The ocular hydrogel implant of any one of items 1 to 9,
wherein the polymer network comprises a plurality of 4- or 8-arm
PEG units. 11. The ocular hydrogel implant of any one of items 1 to
9, wherein the polymer network comprises a plurality of PEG units
having the formula:
##STR00007##
wherein n represents an ethylene oxide repeating unit and the wavy
lines represent the points of repeating units of the polymer
network. 12. The ocular hydrogel implant of any one of items 1 to
11, wherein the polymer network is formed by reacting a plurality
of polyethylene glycol (PEG) units selected from 4a20k PEG-SAZ,
4a20k PEG-SAP, 4a20k PEG-SG, 4a20k PEG-SS, 8a20k PEG-SAZ, 8a20k
PEG-SAP, 8a20k PEG-SG, and 8a20k PEG-SS with one or more PEG or
lysine based-amine groups selected from 4a20k PEG-NH.sub.2, 8a20k
PEG-NH.sub.2, and trilysine, or a salt thereof. 13. The ocular
hydrogel implant of any one of items 1 to 12, wherein the polymer
network is formed by reacting 4a20k PEG-SAZ with 8a20k
PEG-NH.sub.2. 14. The ocular hydrogel implant of any one of items 1
to 13, wherein the polymer network is amorphous (under aqueous
conditions). 15. The ocular hydrogel implant of any one of items 1
to 14, wherein the polymer network is semi-crystalline in the
absence of water. 16. The ocular hydrogel implant of any one of
items 1 to 15, wherein the tyrosine kinase inhibitor is
homogenously dispersed within the polymer network. 17. The ocular
hydrogel implant of any one of items 1 to 16, wherein the tyrosine
kinase inhibitor is released over a period of at least 15 days. 18.
The ocular hydrogel implant of any one of items 1 to 17, wherein
the tyrosine kinase inhibitor is released over a period of at least
30 days. 19. The ocular hydrogel implant of any one of items 1 to
18, wherein the tyrosine kinase inhibitor is released over a period
of at least 60 days. 20. The ocular hydrogel implant of any one of
items 1 to 19, wherein the tyrosine kinase inhibitor is released
over a period of at least 90 days. 21. The ocular hydrogel implant
of any one of items 1 to 20, wherein the tyrosine kinase inhibitor
is released over a period of at least 180 days. 22. The ocular
hydrogel implant of any one of items 1 to 21, wherein the tyrosine
kinase inhibitor is released over a period of at least 365 days.
23. The ocular hydrogel implant of any one of items 1 to 22,
wherein the tyrosine kinase inhibitor is in the form of an
encapsulated microparticle. 24. The ocular hydrogel implant of any
one of items 1 to 23, wherein the tyrosine kinase inhibitor is in
the form of an encapsulated microparticle comprising
poly(lactic-co-glycolic acid). 25. The ocular hydrogel implant of
any one of items 1 to 24, wherein the tyrosine kinase inhibitor is
selected from abemaciclib, acalabrutinib, afatinib, alectinib,
axitinib, barictinib, binimetinib, brigatinib, cabozantinib,
ceritinib, coblmetinib, crizotinib, dabrafenib, dacomitinib,
dasatinib, encorafenib, erlotinib, everolimus, fostamatinib,
gefitinib, gilteritinib, ibrutinib, imatinib, larotrectinib,
lenvatinib, lorlatinib, axitinib, idelalisib, lenvatinib,
midostaurin, neratinib, netarsudil, nilotinib, nintedanib,
osimertinib, palbociclib, pazopanib, ponatinib, regorafenib,
ribociclib, ruxolitinib, sirolimus, sorafenib, sunitinib,
temsirolimus, tofacitinib, trametinib, vandetanib, and vemurafenib.
26. The ocular hydrogel implant of item 1 or 25, wherein the
tyrosine kinase inhibitor is axitinib. 27. The ocular hydrogel
implant of any one of items 1 to 26, wherein the ocular hydrogel
implant is injected into the vitreous humor, injected into the
anterior chamber, or is affixed to the upper or lower punctum of
the eye. 28. A method of treating an ocular condition in a subject
in need thereof, comprising injecting or affixing the ocular
hydrogel implant of any one of items 1 to 27 to the subject. 29.
The method of item 28, wherein the ocular condition is selected
from maculopathies, retinal degeneration, uveitis, retinitis,
choroiditis, vascular diseases, exudative diseases, traumas,
proliferative diseases, infectious disorders, genetic disorders,
retinal tears, holes, and tumors. 30. The method of item 28 or 29,
wherein the ocular condition is selected from age-related macular
degeneration, choroidal neovascularization, diabetic retinopathy,
acute macular neuroretinopathy, central serous chorioretinopathy,
cystoid macular edema, diabetic macular edema, acute multifocal
placoid pigment epitheliopathy, Behcets disease, birdshot
retinochoroidopathy, intermediate uveitis, multifocal choroiditis,
multiple evanescent white dot syndrome (MEWDS), ocular sarcoidosis,
posterior scleritis, serpiginous choroiditis, subretinal fibrosis
and uveitis syndrome, Vogt-Koyanagi-Harada syndrome, Coats disease,
parafoveal telangiectasis, papillophlebitis, frosted branch
angiitis, sickle cell retinopathy, angioid streaks, familial
exudative vitreoretinopathy, sympathetic ophthalmia, uveitic
retinal disease, retinal detachment, proliferative diabetic
retinopathy, ocular histoplasmosis, ocular toxocariasis, viral
retinitis, acute retinal necrosis, ocular syphilis, ocular
tuberculosis, congenital stationary night blindness, cone
dystrophies, retinal detachment, macular hole, giant retinal tear,
solid tumors, posterior uveal melanoma, choroidal hemangioma,
choroidal osteoma, choroidal metastasis, retinoblastoma,
vasoproliferative tumors of the ocular fundus, retinal astrocytoma,
and intraocular lymphoid tumors. 31. The method of item 29 or 30,
wherein the condition is age-related macular degeneration. 32. The
method of any one of items 29 to 31, wherein the subject was
previously treated with an anti-VEGF therapy.
EXAMPLES
[0579] The following Examples are included to demonstrate certain
aspects and embodiments of the invention as described in the
claims. It should be appreciated by those of skill in the art,
however, that the following description is illustrative only and
should not be taken in any way as a restriction of the
invention.
Example 1: Preparation of Axitinib Implants
[0580] The axitinib implants of the present application are
(essentially) cylindrical (and are also referred to herein as
"fibers"), with axitinib homogeneously dispersed and entrapped
within a PEG-based hydrogel matrix to provide sustained release of
axitinib based on its low aqueous solubility in the vitreous humor
of the eye.
[0581] The polymer network of the implants was formed by reacting 2
parts 4a20K PEG-SAZ (a 20 kDa PEG with 4 arms with a
N-hydroxysuccinimidyl reactive end group, sometimes also referred
to as "NHS" end group) with 1 part 8a20K PEG NH2 (a 20 kDa PEG with
8 arms with an amine end group). Therefore, a polyurethane tubing
was cut into appropriate length pieces. After that, an 8a20K PEG
NH2 sodium phosphate dibasic solution was prepared and sterile
filtered to remove endotoxins as well as other particles over 0.2
.mu.m (pore size of the filter). The desired volume of the PEG
amine solution was then weighed into a syringe. Next, corresponding
amounts of solid axitinib depending on the desired final axitinib
dose in the implant were weighed into another syringe. The powdered
axitinib syringe and the PEG amine syringe were mixed carefully to
suspend and disperse the particles. The syringe comprising the
suspension mixture was then sonicated to break up any powdered
agglomerates. After that, a 4a20K PEG SAZ sodium phosphate
monobasic solution was prepared and sterile filtered as described
for the PEG amine solution. The desired volume of PEG SAZ solution
was then weighed into another syringe. In the next step, the
ingredients of both syringes (4a20K PEG SAZ sodium phosphate
monobasic solution and axitinib-8a20K PEG NH2 mixture) were mixed
to initiate the reaction leading to gelation. The liquid suspension
was cast through the prepared polyurethane tubing before the
material cross-links and solidifies. Gelling time was confirmed by
performing a gel tap test. The gel-comprising tubing was then
placed into a high humidity curing chamber for 2 hours in order to
prevent premature drying of the hydrogel prior to hydrogel
gelation. In the chamber, the hydrogel axitinib suspension in the
tubing was allowed to cross-link to completion creating a highly
reacted and uniform gel, thus forming a hydrogel strand.
[0582] After curing, different implant stretching methods were
performed as disclosed herein. Implants were either dry stretched
or wet stretched as outlined below. For dry stretching, strands
were cut into shorter segments after curing and the strands were
dried for 48 to 96 hours. After drying, dried strand segments were
removed from the tubing and placed on clamps of a custom stretcher.
The strands were then slowly dry stretched at a controlled rate to
achieve the desired diameter that fits into a small gauge needle
(stretch factor of about 2 to about 5, or about 3 to about 4.5).
The stretching step was performed in an oxygen and moisture free
environment to protect the product. For wet stretching, strands
were placed on clamps of a custom stretcher. The strands were then
slowly wet stretched at a controlled rate to achieve the desired
diameter that fits into a small gauge needle (stretch factor of
about 1 to about 3, or about 1.3 to about 2.6). After stretching,
the strands were dried under tension under the conditions as
described for the dry stretching process.
[0583] The stretching creates a shape memory, meaning that the
implant upon hydration when administered into the vitreous cavity
of the eye will rapidly shrink in length and widen in diameter
until it approaches its original wet casted dimension. While the
narrow dry dimensions facilitate administration of the product
through a smaller gauge needle, the widened diameter and shortened
length after administration yield a shorter implant (in certain
embodiments not much longer than about 10 mm) in the posterior
chamber relative to the eye diameter minimizing potential contact
with surrounding eye tissues. In general, the degree of shrinking
upon hydration depends inter alia on the stretch factor. For
instance, stretching at e.g. a stretch factor of about 1.3 (wet
stretching) will have a less pronounced effect or will not change
the length during hydration to a large extent. In contrast,
stretching at e.g. a stretch factor of about 1.8 (wet stretching)
will result in a markedly shorter length during hydration.
Stretching at e.g. a stretch factor of about 4 (dry stretching)
could result in a much shorter length upon hydration (such as, for
example, a reduction in length from about 15 to about 8 mm).
[0584] Stretched hydrogel strands were removed from the stretcher
and then cut to the desired final length. The implant fibers were
then placed on the inspection station. If the implants passed the
quality control, they were loaded into a 25 or 27 gauge needle
(e.g. an FDA-approved 25 G UTW 1/2'' having an inner diameter of
about 0.4 mm, or a 25 G UTW 1'' or a 27 G TW 1.25'' needle) using a
customized vacuum device and capped safely to avoid any needle tip
damage.
[0585] The loaded needles were placed into a glove box for 6 to 9
days to remove any moisture (the remaining water content in the
implant is intended to not exceed 1% water). All steps from then on
were performed in the glove box. The loaded needle was dipped into
a melted low-molecular weight 1k PEG to tip the needle. Upon
cooling a hardened small drop of PEG remains, which provides
lubricity, keeps the implant in place within the needle, allows
successful deployment and prevents premature rehydration of the
implant within the needle during administration. Moreover, PEG
tipping is minimizing tissue injury i.e. tissue coring, a process
by which pieces of tissue are removed by a needle as it passes
through the tissue. The PEG-tipped needles were then again
inspected, needles which did not meet the quality requirements were
discarded. Passed needles were again capped to ensure the needles
were not suffering any additional damage. Needles were then
individually pouched and sealed to prevent them from moisture and
keep them sterile. The injection device, for instance a modified
Hamilton glass syringe, had a push wire (e.g. a Nitinol push wire)
that allows deploying the implant from the needle more easily. The
injection needle may contain a stop feature that controls the
injection depth. The injection device can be separately packaged
and sealed under nitrogen in foil pouches in the same way as
described for the needle (FIG. 1), or could be pre-assembled with
the implant-loaded needle or within a preloaded injector. The
packaged needles and injection devices were removed from the glove
box and stored refrigerated (2-8.degree. C.) prior to sterilization
using gamma irradiation. After sterilization the packages were
stored refrigerated (2-8.degree. C.) or frozen protected from light
prior to use and were equilibrated 30 min to room temperature prior
to injection.
[0586] Administration of the implants occurs via intravitreal
injection, wherein the implant localizes in the posterior segment
of the eye (FIG. 2). After injection, the implants hydrate in situ.
Upon hydration upon contact with the vitreous, the implant softens
and increases in diameter and may also shrink in length. By
trapping axitinib into the hydrogel a defined and limited
localization of axitinib in the eye can be provided. The hydrogel
matrix of the implant is formulated to biodegrade via ester
hydrolysis in the aqueous environment of the vitreous. Axitinib
releases for a sustained period from the hydrogel by diffusion into
the vitreous and then into the surrounding ocular tissues based on
the drug's low solubility under physiological conditions (FIG. 3).
The drug release rate from the implants is inter alia influenced by
diffusion, drug clearance, vitreous viscosity, concentration
gradients within and proximate to the implant, implant dose,
implant surface area and geometry, as well as the number of
implants and their localization within the vitreous.
Example 2: In Vitro Axitinib Release
[0587] In a next step, the release rate of axitinib from implants
in different formulations was determined by in vitro testing. The
in vitro assays can be additionally used for quality control of the
implants.
In Vitro Axitinib Release Under Non-Sink Simulated Physiological
Conditions
[0588] In one in vitro assay set-up, axitinib release was evaluated
under non-sink simulated physiological conditions at a daily
replacement volume comparable to the volume of vitreous humor in a
human eye.
[0589] Three exemplarily selected implant formulations were
examined (Table 1). Implant variants #1 and 2 were examined using
one implant, implant variant #3 using one and two implants (four
conditions in total). All conditions were conducted in
duplicate.
TABLE-US-00003 TABLE 1 Formulation, configuration, and
dry-dimensions of three exemplarily selected axitinib implants.
Formulation percentages represent weight by weight (w/w). Implant
variant Implant #1 Implant #2 Implant #3 Formulation Axitinib 61.3%
61.3% 49.4% (amount per (625 .mu.g) (716 .mu.g) (245 .mu.g)
implant) 4a20k PEG-SAZ 21.1% 21.1% 27.7% 8a20k PEG-NH2 10.6% 10.6%
13.8% Sodium Phosphate 1.9% 1.9% 2.5% Monobasic Sodium Phosphate
5.0% 5.0% 6.6% Dibasic Configuration No. of Implants 1 1 1 or 2
Packaging -Implant sealed in foil -Implant sealed in foil -Implant
sealed in foil pouches and sealed pouches and sealed pouches and
sealed under nitrogen. under nitrogen. under nitrogen. -Glass vial
w/5 mL -Glass vial w/5 mL -Glass vial w/5 mL PBS. PBS. PBS. Storage
Frozen Frozen Frozen Dimensions Dried Diameter 0.325 0.499 0.259
(mm) Dried Length (mm) 9.37 7.65 16.47
[0590] Prior to the performance of the in vitro release assay the
starting drug content of the implants was examined by liquid
chromatography coupled to fragmentation-based mass spectrometry
(LC-MS/MS) using ethanol as extraction solvent (Table 2; for
details on implant dissolution and LC-MS/MS reference is made to
Example 3.5). The determined axitinib amounts matched well with the
formulated amounts.
TABLE-US-00004 TABLE 2 Starting axitinib content in the implants as
determined by LC-MS/MS. Condition Axitinib (.mu.g) Implant #1 609
.+-. 48.1 Implant #2 720 .+-. 35.4 Implant #3 .times. 2 458 .+-.
38.9 Implant #3 .times. 1 258 .+-. 33.9
[0591] In vitro released and non-released axitinib was determined
for each group without (control) and with daily release media
sampling.
[0592] For control implant release, samples were placed in tubes.
Five mL of PBS (pH 7.2) were added to each tube on day 0 and the
tubes were covered with a lid. Samples were then placed in a
37.degree. C. incubator and gently rocked for 20 (1.times. implant
#3) or 30 days (implant #1 and #2, 2.times. implant #3). At the end
of the test period, the PBS was removed (1 mL PBS was saved for
testing). One mL of ethanol was added to the residual sample. Both
PBS samples and residual samples were tested for axitinib amount
released.
[0593] For daily implant release, samples were placed in tubes.
Five mL of PBS were added to each tube on day 0 and the tubes were
covered with a lid. Samples were then placed in a 37.degree. C.
incubator and rocked gently. After 24 hours, 4 mL of PBS were
removed from each sample from which 1 mL was used for testing and
the remaining 3 mL were disposed. Four mL of fresh PBS were added
back into each tube. This process was repeated for 20 (1.times.
implant #3) or 30 days (implant #1 and #2, 2.times. implant #3). On
the final day of the study, 1 mL of PBS was used for testing each
sample and the remaining 4 mL were disposed. One mL of ethanol was
added to the remaining residual implants and was tested for total
remaining axitinib.
[0594] The axitinib concentration in PBS from control implant
release measurements after 20 or 30 days, respectively, represented
a maximal solubility determination of axitinib after prolonged
incubation in the release media (Table 3). The higher dose
strengths resulted in higher axitinib concentrations in the release
media. The apparent maximal axitinib solubility ranged from 0.24 to
0.40 .mu.g/mL, which was consistent with results reported in the
literature for INLYTA.RTM. [NDA 202324].
TABLE-US-00005 TABLE 3 Control release data. Axitinib amounts and
concentrations are presented as mean and standard deviation (SD).
Total Axitinib Axitinib Axitinib concentration Remaining Released
in media Condition (.mu.g) (.mu.g) (.mu.g/mL) Implant #1 595 .+-.
42.4 2.01 .+-. 0.004 0.40 .+-. 0.707 Implant #2 679 .+-. 48.8 1.90
.+-. 0.007 0.38 .+-. 1.41 Implant #3 .times. 2 458 .+-. 50.9 1.21
.+-. 0.032 0.24 .+-. 6.36 Implant #3 .times. 1 251 .+-. 35.4 1.35
.+-. 0.449 0.27 .+-. 89.8
[0595] Test results demonstrated that the two high dose samples
(implants #1 and 2) released more axitinib per day than the lower
dose groups (Table 4). The amount of axitinib released per day over
the study duration is presented in FIG. 4A. The amount of total
axitinib released was higher in the groups that removed and
replaced PBS daily compared to the no PBS exchange (control).
Implants #1 and #2 released more axitinib per day than two implants
of implant #3. The mean value of total axitinib released was
slightly different in both high dose groups, but the median amounts
released daily were comparable, indicating no apparent difference
between the two higher dose groups.
TABLE-US-00006 TABLE 4 Daily sampling data. Axitinib amounts are
presented as mean and standard deviation (SD). Total Axitinib
Axitinib Axitinib Daily Remaining Released Released Condition
(.mu.g) (.mu.g) (.mu.g) Implant #1 566 .+-. 43.8 10.44 .+-. 0.35
0.36 .+-. 0.049 Implant #2 622 .+-. 43.8 11.48 .+-. 0.38 0.36 .+-.
0.073 Implant #3 .times. 2 456 .+-. 16.3 5.26 .+-. 0.18 0.16 .+-.
0.044 Implant #3 .times. 1 231 .+-. 6.36 2.26 .+-. 0.11 0.11 .+-.
0.019
[0596] The study results demonstrate that a single administration
of an implant containing approximately 0.6 to 0.7 mg of axitinib
releases more axitinib per day into solution in simulated
physiological conditions under non-sink conditions at a volume
representative of the vitreous humor eye volume compared to the one
or two lower dosage total strengths. Two implants containing
approximately 0.2 mg each didn't release as much axitinib as a
single higher dose implant under these conditions. These in vitro
results indicate that a single implant at a higher dose may release
more axitinib per day in the eye in the non-sink conditions of the
eye than two implants of a lower total dose.
In Vitro Axitinib Release Under Real-Time Sink Simulated
Physiological Conditions
[0597] In another in vitro set-up, axitinib release was evaluated
under real-time sink simulated physiological conditions.
[0598] Therefore, implants were placed in 5 mL of a physiologically
relevant media, i.e. PBS, pH 7.2 with 0.01% NaF with a layer of
1-octanol on top of the solution to provide a sink phase allowing
transference of the axitinib into the octanol layer. Implants were
incubated under mild agitation at 37.degree. C. in an air chamber.
Axitinib was measured at pre-determined sampling time points in the
octanol layer by taking the UV absorbance at 333 nm. The amount of
axitinib released at each time point is determined relative to a
standard curve prepared from an axitinib reference. The accelerated
in vitro release profile is determined as the percent of cumulative
release of axitinib. The duration to complete drug release was
several months.
[0599] For an exemplarily release profile under real-time sink
conditions reference is made to FIG. 14A.
In Vitro Axitinib Release Under Accelerated Conditions
[0600] In a further in vitro set-up, axitinib release was evaluated
under accelerated conditions.
[0601] Therefore, the implants were placed into an ethanol and
water mixture (25:75 ratio, v/v) to increase axitinib solubility at
37.degree. C. in an air chamber with mild agitation. The solubility
of axitinib in pure ethanol is 1.4 mg/mL and is approximately 19
.mu.g/mL in a 25% ethanol/75% water mix (v/v; physiologically non
relevant media). At pre-determined sampling time points, an aliquot
is removed and analyzed for axitinib by taking the UV at 332 nm.
The amount of axitinib released at each time point is determined
relative to a standard curve prepared from an axitinib reference.
The accelerated in vitro release profile is determined as the
percent of cumulative release of axitinib. The duration of release
under accelerated conditions is approximately two weeks.
[0602] For an exemplarily release profile under accelerated
conditions reference is made to FIG. 14B (200 .mu.g implant) and
FIG. 4B (556 .mu.g implant).
Example 3: Evaluation of Axitinib Implants in Rabbits
[0603] In order to evaluate safety, tolerability, drug release, as
well as efficacy of axitinib implants, several pre-clinical studies
in Dutch belted rabbits were performed. A broad range of doses were
examined either delivered by one or more implants. An overview of
the different rabbit studies performed is presented in Table 5.
Further studies were performed in beagle dogs and African green
monkeys.
TABLE-US-00007 TABLE 5 Overview of pre-clinical studies with
axitinib implants in rabbits. Drug dose and number of implants
Example per eye (bilaterally) Study purpose No. Primary low-dose
screen 15 .mu.g axitinib in one implant; Safety, tolerability, 3.1
administration of one, two, or and efficacy at low dose three
implants Administration of one implant 227 .mu.g axitinib in one
implant; Tolerability, safety 3.2 administration of one implant and
efficacy Administration of two implants 128 .mu.g axitinib per
implant, Tolerability and safety 3.3 total dose of 256 .mu.g;
administration of two implants Administration of two implants
either with or without co-administration of Avastin .RTM. 145 .mu.g
axitinib per implant, Tolerability, safety and 3.4 total dose of
290 .mu.g; efficacy with and without administration of two implants
co-administration of anti-VEGF drug Drug release from axitinib
implants 109 .mu.g axitinib in one implant; Monitoring drug release
3.5 administration of one implant from the implants in 227 .mu.g
axitinib in one implant; different eye tissues; administration of
one implant Evaluation of systemic 145 .mu.g axitinib per implant,
axitinib concentration total dose of 290 .mu.g; administration of
two implants 145 .mu.g axitinib per implant, total dose of 290
.mu.g with Avastin .RTM.; administration of two implants Acute
exposure to axitinib 600 .mu.g axitinib suspension Evaluation of
safety of 3.6 injected intravitreal an axitinib bolus dose
[0604] Table 6 gives an exemplarily overview of formulations,
configurations, and dimensions of implants used in animal studies
(cf. Examples 3.2 to 6). The dimensions of hydrated implants were
examined after 24 hours in biorelevant media (PBS, pH 7.2 at
37.degree. C.). Although implant #5 showed a slight increase in
length, the hydrated length was still below 10 mm.
TABLE-US-00008 TABLE 6 Formulation, configuration, and dimensions
of different implants (#1 to #5) as used in animal studies. For
instance, implant #4 was used for African green monkey studies (cf.
Example 5). Formulation percentages represent weight by weight
(w/w). Implant type Implant #1 Implant #2 Implant #3 Implant #4
Implant #5 Formulation Axitinib 54.6% 54.7% 58.1% 54.8% 38.0%
(amount per implant) (128 .mu.g) (145 .mu.g) (227 .mu.g) (138
.mu.g) (109 .mu.g) PEG Hydrogel 37.2% total 37.1% total 29.1% total
37.0% total 50.9% total 4a20K PEG-SAZ 24.8% 24.7% 19.4% 24.7% 33.9%
8a20K PEG-NH2 12.4% 12.4% 9.7% 12.3% 17.0% Sodium phosphate 8.2%
8.2% 12.8% 8.1% 11.1% Configuration Stretching Method Dry Dry Dry
Dry Wet Needle Size 27G TW 1.25'' 27G TW 1.25'' 25G UTW 1'' 25G UTW
1'' 27G TW 1.25'' Injector/Syringe 10 .mu.L Modified 10 .mu.L
Modified 50 .mu.L Modified 50 .mu.L Modified Implant Hamilton
Hamilton Hamilton Hamilton Injector Packaging Foil Pouches Foil
Pouches Foil Pouches Foil Pouches Foil Pouches Push Wire Nitinol
Wire Nitinol Wire Teflon Teflon Nitinol Wire Stainless Steel
Stainless Steel Wire Wire Sterilization Type Gamma Gamma Gamma
Gamma Gamma Site Storage Refrigerated Frozen Refrigerated
Refrigerated Refrigerated Dimensions Dried Diameter 0.20 mm 0.24 mm
0.24 mm 0.24 mm 0.2 mm Length 12.4 mm 12.3 mm 12.5 mm 12.6 mm 7.0
mm Hydrated Diameter 0.63 mm 0.64 mm 0.65 mm 0.67 mm 0.5 mm Length
5.1 mm 5.2 mm 5.5 mm 4.9 mm 9.2 mm
[0605] Prior to implant administration, animals were anesthetized
with an intramuscular injection of ketamine hydrochloride (20
mg/kg) and xylazine (5 mg/kg). Eyes and the surrounding area were
cleaned with a 5% Betadine solution and rinsed with balanced salt
solution. One to two drops of topical proparacaine hydrochloride
anesthetic (0.5%) was applied. The eye was draped, and a sterile
wire speculum was placed to retract the eyelids. The injection
needle was placed approximately 3 to 5 mm away from the limbus and
deployed in a single stroke.
[0606] In summary, the axitinib implants showed a good safety
profile, were well tolerable and highly effective independent of
the dose or way of delivery (by one or more implants). Moreover,
the drug was efficiently released in target tissues, while systemic
concentrations in blood remained very low or undetectable.
Example 3.1: Primary Low-Dose Screen of Axitinib Implants
[0607] For primary safety, tolerability, and efficacy investigation
of the axitinib-containing implants, a low dose of 15 .mu.g
axitinib per implant was administered as either one (group 1, n=5),
two (group 2, n=5) or three implants (group 3, n=5) per eye
bilaterally via intravitreal injection using a 30 G 0.5'' needle in
rabbits including control animals receiving saline. The implants
used in this study had a diameter of 0.15.+-.0.13 mm and a length
of 6.9.+-.0.1 mm in a dried state. After hydration for 24 hours in
biorelevant media (PBS, pH 7.2 at 37.degree. C.) the diameter was
0.42.+-.0.02 mm and the length was 10.6.+-.0.4 mm.
[0608] Over a time of 1 month, general health, body weights, and
intraocular pressure (IOP) were recorded. Clinical ophthalmic exams
were scored at baseline and at 1 month according to the modified
McDonald-Shadduck scoring system (McDonald, T. O., and Shadduck, J.
A. "Eye irritation". Advances in Modern Toxicology, IV:
Dermatotoxicology and Pharmacology, 1977). Infrared reflectance
(IR) imaging was collected at 1 month for representative images of
the one, two and three implants in the vitreous. Ocular
distribution of axitinib was examined using LC-MS/MS essentially as
described under Example 3.5. In order to evaluate efficacy of the
implants, the rabbits with and without implants were challenged by
recurring intravitreal injection of VEGF to induce retinal vascular
leakage essentially as described under Example 3.2.
[0609] No notable effects on body weight were observed in none of
the groups. Moreover, IOP values were normal and comparable between
all groups. Ocular health was not or only mildly affected
indicating overall safety and tolerability. Clinical ophthalmic
examinations at one-month demonstrated no ocular findings for any
animals administered a single implant. Mild corneal opacity was
observed in one eye of animals administered two or three implants.
Mild and moderate conjunctival discharge was observed in two eyes
of animals administered three implants.
[0610] IR imaging revealed that the overall shape of the implants,
independently of the number administered, remained intact (FIG.
5A).
[0611] Pharmacokinetic results of axitinib concentrations in the
ocular tissues at 1 month for each group are presented in Table 7.
Two eyes were excluded from analysis because one eye in the retina
tissue samples in group 2 and one eye in the choroid/RPE (retinal
pigment epithelium) samples in group 3 likely included a portion of
the implant creating erroneously high concentrations in those two
tissue samples due to preferential dissolution in the extraction
organic solvent system employed prior to LC-MS/MS analysis (cf.
Example 3.5). The solubility of axitinib in PBS, pH 7.2 at
37.degree. C. was determined to be approximately 0.5 .mu.g/mL and
any tissue values markedly higher than this potentially indicates
either tissue accumulation or sample contamination. Axitinib
concentrations were either low or absence in the AH compared to the
other ocular tissues indicating little migration of axitinib from
the posterior chamber to the anterior chamber. The ocular
distribution results demonstrated that a single implant dose (group
1) appeared to be almost fully depleted at 1 month with only 0.3
.mu.g remaining in the VH. 25.5 .mu.g were released from the 30
.mu.g starting dose (two implants, group 2) over the first month
for a daily release rate of approximately 0.8 .mu.g/day. 33.8 .mu.g
were released from the 45 .mu.g starting dose (three implants,
group 3) over the first month for a daily release rate of
approximately 1.1 .mu.g/day. Median axitinib levels in the retina
were 31 ng/g for group 1, 65 ng/g for group 2 and 148 ng/g for
group 3 demonstrating a dose dependent release into the retina
tissue. Saturation was not achieved in this study.
TABLE-US-00009 TABLE 7 Ocular tissue distribution of axitinib
released from 1, 2, and 3 implants with an axitinib dose of 15
.mu.g per implant (groups 1, 2, and 3, respectively). Axitinib
concentrations in AH, retina, and choroid/RPE, as well as remaining
axitinib in the implant (recovered from the VH) are presented after
1 month as average (mean) including standard deviation, coefficient
of variation (CV) as well as the confidence interval (CI) of the
mean. In addition, minimum, median, and maximum values for each
data point are presented. N 95% Tissue Group Eyes Average Min.
Median Max. SD CV CI AH 1 10 0.1 0.0 0.0 0.3 0.1 213% 0.1 (ng/mL) 2
9 0.1 0.0 0.0 0.3 0.1 203% 0.1 3 9 0.1 0.0 0.0 0.2 0.1 198% 0.1
Retina 1 10 43 18 31 108 30 69% 18 (ng/g) 2 9 86 39 65 230 59 69%
39 3 9 200 64 148 455 123 61% 80 1 10 95 0 32 464 151 159% 94
Choroid/RPE 2 9 154 0 104 332 115 75% 75 (ng/g) 3 9 175 49 110 526
156 89% 102 1 10 0.4 0.0 0.3 1.1 0.4 97% 0.2 VH + Implant 2 9 4.4
1.2 4.5 7.3 2.2 50% 1.5 (.mu.g) 3 9 11.2 6.3 11.2 16.9 3.4 30%
2.2
[0612] Of note, all three doses demonstrated inhibition of vascular
leakage after the VEGF challenge at one month compared to control
animals (n=3) not having an implant indicating that even the lowest
dose (15 .mu.g) exhibited good efficacy even after short times of 1
month (FIG. 5B).
[0613] In summary, the TKI implants administered either as one,
two, or three implants per eye were successfully validated for
safety, tolerability, as well as axitinib release and efficacy in
the primary low dose study.
Example 3.2: Tolerability, Safety and Efficacy Studies with One
Axitinib Implant
[0614] In order to study the tolerability, safety and efficacy of
one implant per eye with a higher axitinib dose, rabbits were
administered bilaterally via intravitreal injection with a 25 G
ultra-thin wall needle one implant per eye with an axitinib dose of
227 .mu.g. For implant dimension reference is made to Table 6
(implant type #3).
Tolerability and Safety
[0615] For tolerability and safety studies, 9 animals were
monitored over 6 months for general health (daily), body weight (0,
1, 3, 6 months) and IOP and ophthalmic exams (each in 0.5 months
intervals). Clinical ophthalmic exams were scored according to the
modified McDonald-Shadduck scoring system. Electroretinography
(ERG) and fluorescein angiography (FA) were performed at 1, 3, and
6 months to assess retinal function and to evaluate the vasculature
of the eye, respectively. Optical coherence tomography (OCT) was
performed monthly to obtain cross-sectional images of the retina.
IR imaging was performed monthly to monitor biodegradation of
implants over the time and persistence of axitinib in the
vitreous.
[0616] Upon sacrifice (3 animals at 1, 3, and 6 months), whole eyes
were prepared for histopathological analysis. Therefore, a suture
was placed at the 12 o'clock position for orientation and harvest.
Typically, eyes were trimmed in half in the plane from 12 o'clock
to 6 o'clock through the lens and optic nerve along the midline.
This captures as many optic structures in one plane as possible.
The trimmed eyes were examined grossly and abnormalities noted.
Hematoxylin and eosin (H&E)-stained slides were prepared that
were separated by 1 mm. Each slide contained 2 serial sections.
Histopathology assessments at each time point included vitreous,
retinal, scleral, or episcleral inflammation, retinal disruption
and fibrosis around the injected area. Scoring was performed on a
semi-quantitative scale from 0-5 for any abnormalities, where 0
denotes no change (normal), 1 denotes rare foci of change
(minimal), 2 denotes mild diffuse change or more pronounced focal
change, 3 denotes moderate diffuse change, 4 denotes marked diffuse
change and 5 denotes severe diffuse change.
[0617] No notable effects on daily health or body weights were
observed. IOP was normal for the complete duration of the study. No
notable effects from the implants were found based on
electroretinography (ERG) measurements. Fluorescein angiography
(FA) and OCT imaging revealed no pathologies over the study. For
instance, normal retinal morphology was preserved over 6 months
(FIG. 6). In addition, ophthalmic exam findings were normal or
mild. IR imaging at weeks 4 and 8 revealed an intact implant,
whereas images at week 12 demonstrated early stages of hydrogel
degradation (FIG. 7A). Images at week 16 showed implant narrowing
due to loss of hydrogel structure. Finally, images at weeks 20 and
26 showed the absence of hydrogel, while non-dissolved axitinib
particles remained in proximity to the former implant site and
formed a single monolithic structure. However, any undissolved
axitinib remaining at the implant site was shown to continue to
release axitinib at levels sufficient for inhibition of vascular
leakage (as demonstrated for instance through 21 months in a
VEGF-challenge study, see Example 3.4). In addition, no
inflammation was observed in the region of undissolved axitinib
particles (FIG. 7B).
[0618] The amount of axitinib decreased in the histopathology
sections over time indicating bio-resorption of the injected
material. There were no observations of gross lesions in the
sections noted over the study duration. Mean histopathology results
with standard deviations are presented in Table 8. Mean
inflammation scores showed that retinal, scleral, or episcleral,
vitreous chamber and chronic subcorneal (lymphocytes and phagocytes
at cornea edges) inflammation scores were normal to minimal over
the study duration. Mean fibrosis scores around the injected test
article were normal to minimal over the study duration. Mean
retinal disruption scores were minimal over the study duration.
Mean retinal vacuolization scores were minimal over the study
duration. Retinal detachments were not observed clinically, but
were noted in 1 of 68, 5 of 71, and 1 of 72 histologic sections for
months 1, 3 and 6, respectively. The position of the detachments
was often associated with retinal disruption sites and are
consistent with the needle penetration site position, indicating
that they were likely procedure related.
TABLE-US-00010 TABLE 8 Histopathological analysis results for
rabbits with one implant (227 .mu.g axitinib per implant). Results
were scored on a scale of 0-5, where 0 denotes no change (normal),
1 denotes rare foci of change (minimal), 2 denotes mild diffuse
change or more pronounced focal change, 3 denotes moderate diffuse
change, 4 denotes marked diffuse change and 5 denotes severe
diffuse change. Results are presented as mean and standard
deviation (SD). Retinal, Scleral, or Fibrosis Chronic Retinal
Retinal Vitreous Chamber Episcleral Around the Subcorneal Month
Disruption Vacuolization Inflammation Inflammation Implant
Inflammation 1 0.03 (0.06) 0.40 (0.24) 0.07 (0.16) 0.02 (0.04) 0.02
(0.04) 0.02 (0.04) 3 0.05 (0.06) 0.57 (0.21) 0.07 (0.05) 0.18
(0.05) 0.00 (0.00) 0.10 (0.20) 6 0.03 (0.05) 0.82 (0.25) 0.30
(0.28) 0.05 (0.08) 0.03 (0.05) 0.40 (0.20)
Efficacy
[0619] For efficacy studies, 12 animals (with and without the
implant) received an intravenously VEGF challenge (1 .mu.g) 48
hours prior to selected time points (1, 2, 3, and 6 months after
implant injection; 3 animals euthanized at each time point) to
induce vascular proliferation and leakage. Rabbits were followed
for 6 months from the administration of the implant. Eyes were
imaged 48 hours post VEGF challenge using fluorescein angiography
(FA) after intravenous injection of fluorescein and were graded on
a scale from 0 to 4 (Table 9). Each eye was scored on the left and
right side to account for non-uniformity in inflammatory response.
FA scores were then averaged for each eye.
TABLE-US-00011 TABLE 9 Description of scoring method for imaging by
fluorescein angiography (FA). Score Description 0 Normal eye,
vessels appear straight and simple, no haziness or leakage 1 Some
minor tortuosity, but generally vessels appear straight, no
haziness or leakage 2 Some more advanced tortuosity, vessels appear
choked and a lot of branching is visible, but still no haziness or
leakage 3 Extreme tortuosity, vessels appear choked and a lot of
branching is visible, some slight haziness pointing to leakage of
the vessels 4 Extreme tortuosity and extreme leakage, eye appears
as a haze and vessels are difficult to visualize
[0620] Vascular leakage was effectively reduced in animals with the
implant when compared to control animals that received saline
instead of the implant over a period of 6 months (FIG. 8). Blank
control eyes showed high tortuosity and leakage at all
time-points.
[0621] Taken together, the data demonstrate good tolerability and
safety of one higher dose implant, as well as suitable
biodegradation rates and the potential of the implant to inhibit
neovascularization in vivo.
Example 3.3: Tolerability and Safety Studies with Two Axitinib
Implants
[0622] In a next step, tolerability and safety of two implants with
higher axitinib dose (128 .mu.g per implant, total dose of 256
.mu.g per eye) were investigated. Therefore, rabbits (n=9) received
two implants (implant type #1 in Table 6) bilaterally with a total
axitinib dose of 256 .mu.g (128 .mu.g per implant) via intravitreal
injection with a 27 G ultra-thin wall needle.
[0623] Over a study period of 6.5 months, rabbits were daily
monitored for health, IOP, and body weight. Clinical ophthalmic
exams (daily) were scored according to the modified
McDonalds-Shadduck scoring system. Optical coherence tomography
(OCT) was performed to obtain cross-sectional images of the retina
(monthly). Infrared (IR) imaging was performed to monitor the
persistence and degradation of implants and axitinib in the
vitreous (monthly). Electroretinography (ERG) was performed to
assess retinal function and fluorescein angiography (FA) was
performed to evaluate the vasculature of the eye at months 1, 3,
and 6.5. At months 1, 3, and 6.5, each 3 rabbits were sacrificed.
After sacrifice, whole eyes were prepared for histopathological
analysis (cf. Example 3.2).
[0624] No abnormal general health observations were observed. All
rabbits either gained or maintained weight over the study duration.
Ocular health findings were limited to irritation, swelling, and/or
discharge that were sporadic, generally mild and transient.
Clinical ophthalmic examinations demonstrated no ocular
abnormalities over the course of the study, except of mild
conjunctival discharge for half of the animals at day 14, likely
procedure related, which resolved by day 27, a single instance of
mild retina hemorrhage immediately post-administration which
resolved by day 27, mild conjunctival congestion seven weeks post
administration, and lens opacity due to attachment of the implant
to the lens in one eye at day 195. IOP was normal for the duration
of the study. OCT imaging revealed no retinal abnormalities over
the study duration. ERG was normal for all study eyes, indicating
normal retinal function. FA found normal vascularization and no
evidence of dilation or leakage.
[0625] IR imaging demonstrated hydrogel degradation of the two
implants over time and a more monolithic morphology was formed as
the axitinib particles were released from the confines of the
hydrogel, as seen post day 117 (FIG. 9). These observations were
similar to the implant behavior in Example 3.2 (FIG. 7A).
[0626] Histopathology noted that the amount of the test article
declined in the sections over time, indicating bioresorption of the
injected material. Histopathological findings assessing
inflammation and fibrosis were absent or minimal over the study
duration. Mean histopathology results with standard deviations are
presented in Table 10. Mean histopathological inflammation scores
showed that retinal, scleral, or episcleral, vitreous chamber and
chronic subcorneal (lymphocytes and phagocytes at cornea edges)
inflammation scores were normal to minimal over the study duration.
Mean fibrosis scores around the injected test article were normal
to minimal over the study duration. Mean retinal disruption scores
were normal to minimal over the study duration. Mean retinal
vacuolization scores were minimal over the study duration. Retinal
detachments were not observed clinically, but were noted in 2 of
192 histologic sections for months 1, 3, and 6, respectively. The
position of the detachments was often associated with retinal
disruption sites and are consistent with the needle penetration
through the retina at the injection location indicating that they
were likely procedure related.
TABLE-US-00012 TABLE 10 Histopathological analysis results for
rabbits with two implants (total dose of 256 .mu.g axitinib per
eye). Results were scored on a scale of 0-5, where 0 denotes no
change (normal), 1 denotes rare foci of change (minimal), 2 denotes
mild diffuse change or more pronounced focal change, 3 denotes
moderate diffuse change, 4 denotes marked diffuse change and 5
denotes severe diffuse change. Results are presented as mean and
standard deviation (SD). Vitreous Retinal, Scleral, Fibrosis
Chronic Retinal Retinal Chamber or Episcleral Around Subcorneal
Month Disruption Vacuolization Inflammation Inflammation the
Implant Inflammation 1 0.03 (0.06) 0.50 (0.31) 0.15 (0.23) 0.02
(0.04) 0.00 (0.00) 0.58 (0.31) 3 0.00 (0.00) 0.36 (0.39) 0.06
(0.09) 0.00 (0.00) 0.00 (0.00) 0.58 (0.48) 6.5 0.02 (0.04) 0.28
(0.41) 0.02 (0.04) 0.04 (0.05) 0.02 (0.04) 0.42 (0.38)
Example 3.4: Tolerability, Safety and Efficacy Studies with Two
Axitinib Implants with or without Co-Administration of
Avastin.RTM.
[0627] In a next step, the tolerability, safety and efficacy of two
axitinib implants (145 .mu.g axitinib resulting in a dose of 290
.mu.g per eye) bilaterally administered via intravitreal injection
with a 27 G ultra-thin wall needle was assessed with and without
co-administration of 1.25 mg Avastin.RTM. (bevacizumab). For the
animals receiving Avastin.RTM., the anti-VEGF therapeutic was
administered intravitreally followed by administration of the two
implants. For formulation and dimensions of the implants applied in
this study, reference is made to Table 6 (implant type #2).
Tolerability and Safety
[0628] For tolerability and safety studies, 30 rabbits (n=15 per
group, wherein group 1 did not receive Avastin.RTM. and group 2
received 1.25 mg Avastin.RTM.) were monitored for a study time of
up to 38 months. General health was checked on a daily basis until
31 months and body weight was checked on a daily basis until 21
months. In addition, IR imaging was performed to monitor
persistence and degradation of the implants and axitinib in the
vitreous over 38 months. Ophthalmic exams and IOP were monitored
for 21 months. Ophthalmic exams were scored according to the
modified McDonald-Shadduck scoring system.
[0629] In summary, no effects on body weight were observed. Daily
general health observations solely revealed limited to mild ocular
findings which self-resolved. IOP and ocular exams were normal
throughout the study. Ophthalmic findings were generally mild in
nature for vitreous flare, choroidal/retinal inflammation, and
conjunctival discharge. All findings were comparable between
implants applied with or without co-administration of Avastin.RTM.
demonstrating the suitability of the implants to be combined with
other therapeutics such as anti-VEGF medicals.
[0630] IR imaging confirmed that the implants dissociated over the
study duration and demonstrate hydrogel degradation of the two
implants over time and a more monolithic morphology was observed as
the axitinib particles merge into a single monolithic structure
between 6 and 9 months, wherein the structure demonstrated a
reduction in size through study completion (FIG. 10). These
observations were also in line with images from Examples 3.2 and
3.3 (FIGS. 7A and 9).
Efficacy
[0631] For efficacy studies, 52 rabbits were divided in 4 groups,
wherein group 1 received the two implants but did not receive
Avastin.RTM. (n=15), group 2 received the two implants and received
Avastin.RTM. (n=15), group 3 solely received Avastin.RTM. (n=9),
and group 4 were control rabbits without implant receiving saline
(n=13). Animals from each group were intravenously challenged with
VEGF (1 .mu.g) 48 hours prior to selected time points (0.5, 1, 3,
6, 9, 12, 14, 16, 19, 20, and 21 months) to induce vascular
proliferation and leakage. Eyes were imaged 48 hours post VEGF
challenge time-points using fluorescein angiography (FA) and were
graded on a scale from 0 (normal) to 4 (severe leakage) as
described under Example 3.2.
[0632] It was demonstrated that vascular leakage was prevented with
and without the co-administration of Avastin.RTM. for up to 21
months with repeated VEGF challenges (FIG. 11). Representative FA
images at 1 month post implant injection clearly show effective
leakage inhibition 1 month after implant injection for animals of
group 2 (FIG. 12). Of note, animals solely receiving Avastin.RTM.
(group 3) showed rapid leakage inhibition within the first 2 and 4
weeks, however, after 3 months vascular leakage re-occurred to a
similar degree than observed in the control animals (group 4; FIG.
13). Blank control eyes showed high tortuosity and leakage at all
time-points (Score 3-4).
[0633] Taken together, the VEGF challenging data demonstrated the
potential of the implants to inhibit neovascularization in vivo in
line with the good efficacy resulting from one implant (cf. Example
3.2). Compared to animals solely receiving Avastin.RTM., the
beneficial effect of the implants was demonstrated. In contrast to
the anti-VEGF therapeutic where effects only lasted until 3 months
post injection, the implants enabled a long-term inhibition of
neovascularization of up to 21 months.
Example 3.5: Axitinib Release from Implants and Axitinib
Distribution in Rabbits
[0634] Finally, pharmacokinetic studies have been performed in
order to evaluate drug-release from the implants and axitinib
distribution to the ocular tissues, specifically the retina,
choroid/retinal pigment epithelium (RPE), vitreous humor (VH) and
aqueous humor (AH) over time following sustained release from the
implants. In addition, systemic axitinib concentrations were
monitored. Therefore, rabbits were divided into 4 groups. 2 groups
received bilaterally one implant comprising either 109 .mu.g
axitinib (group 1, n=14) or 227 .mu.g axitinib (cf. Example 3.2,
Group 2, n=24). Group 3 (cf. Example 3.4; n=15) received
bilaterally two implants, each comprising 145 .mu.g, i.e., a total
dose of 290 .mu.g axitinib. Group 4 (cf. Example 3.4; n=15)
received bilaterally two implants comprising, as for group 3, a
total dose of 290 .mu.g axitinib (2.times.145 .mu.g) and in
addition 1.25 mg Avastin.RTM. (bevacizumab) intravitreal.
Formulations, configurations, and dimensions of implants with
corresponding axitinib doses are presented in Table 6.
[0635] For investigation of drug release, two rabbits were
euthanized per time-point for group 1 (day 1 and 1.5, 3, 4.5, 6,
7.5 and 9 months), six rabbits were euthanized per time-point for
group 2 (1, 3, 6, and 7 months), and 3 (0.5, 1, 3, and 6 months)
and 1 (9 and 38 months) rabbits were euthanized per time-point for
groups 3 and 4. In addition, blood samples were taken from the
rabbits prior to euthanasia at time points indicated in Table
11.
Methods: Determination of Axitinib in Plasma
[0636] For determination of axitinib in plasma, two equivalent
quantification methods were carried out. Axitinib was extracted
from plasma by supported liquid extraction (SLE) and was dried
under nitrogen. The short-term matrix (plasma) stability was up to
4 hours and the extract stability was up to 116 hours.
[0637] After reconstitution in methanol/water (50:50 v/v; method 1)
or alternatively in methanol/water/formic acid (75:25:0.01 v/v/v;
method 2), the samples were analyzed by liquid
chromatography-tandem mass spectrometry (LC-MS/MS; API 4000,
Applied Biosystems) using a water/formic acid/methanol gradient.
Axitinib and the internal standard (IS; axitinib-D3 for method 1
and pazopanib for method 2) were separated on an YMC-Pack Pro C4
column (50.times.3.0 mm I.D.; method 1) or a Phenomenex Luna C18
column (method 2) and quantitated using electrospray ionization
(ESI) selective reaction monitoring mode with a total run time of
approximately 6 min. For quantification, the peak area of axitinib
(m/z 387.2 to 356.0) and the IS (m/z 390.2 to 356.0 for axitinib-D3
and m/z 438.2 to 357.1 for pazopanib) were determined and compared
to a standard curve, which showed linear behavior in the desired
concentration range and a correlation coefficient (r.sup.2) of
>0.99. The lower limit of quantitation (LLOQ) ranged from about
0.01 ng/mL to about 0.36 ng/mL depending on the study group and
sampling time-points (Table 11).
TABLE-US-00013 TABLE 11 Sampling time points and corresponding LLOQ
(by isomer) for axitinib in plasma or serum. For group 1, plasma
samples were analyzed on day 1 and 1.5, 3, 4.5, 6, 7.5 and 9
months. For group 2, plasma samples were analyzed after 3, 6, and 7
months. For groups 3 and 4, serum samples were analyzed after 6
months. Study Group Sampling time points (LLOQ depending on isomer)
Group 1 Day 1 and 1.5, 3, 4.5, 6, 7.5 and 9 months (0.0500 ng/mL;
both isomers) Group 2 -3 months (0.355 ng/mL (trans), 0.146 ng/mL
(cis)) -6 months (0.0717 ng/mL (trans), 0.0283 ng/mL (cis) -7
months (0.0158 ng/mL (trans), 0.0106 ng/mL (cis)) Groups 3 and 4 6
months (0.0452 ng/mL (trans), 0.00970 ng/mL (cis))
Methods: Determination of Axitinib in Ocular Tissues
[0638] For determination of axitinib concentrations in ocular
tissues, eyes were enucleated and frozen in liquid nitrogen at the
selected time points (Table 13). The eyes were stored frozen prior
to frozen dissection and subsequent bioanalysis. For determination
of axitinib in ocular tissues, two equivalent quantification
methods were carried out. Equivalency of both methods to determine
the axitinib concentrations in AH, VH, retina and choroid
homogenate was demonstrated during qualification.
[0639] Ocular tissue samples of retina and choroid were homogenized
in a methanol/water diluent (50:50, v/v; method 1) or in phosphate
buffered saline (PBS; method 2) in tubes containing ceramic beads.
Soluble axitinib in VH and AH was diluted directly from the samples
with methanol/water diluent (50:50, v/v) and vitreous humor samples
containing the implant (undissolved axitinib) were extracted with
ethanol (method 1). In method 2, homogenized tissues, soluble
axitinib in VH and AH were diluted with methanol/water/formic acid
(75:25:0.01 v/v/v). Analyte was extracted from the matrix by
protein precipitation (method 1) or SLE (method 2), respectively.
The short-term matrix stability was up to 5 hours (AH), up to 5.5
hours (VH), up to 6.6 hours (retina) and up to 4.5 hours (choroid).
The extract was stable up to 171 hours (AH), up to 153 hours (VH),
up to 115 hours (retina) and up to 114 hours (choroid).
[0640] Samples were dried under nitrogen and reconstituted with
methanol/water (50:50 v/v) and are analyzed via LC-MS/MS (API 4000,
Applied Biosystems) with a water/formic acid/acetonitrile gradient
(method 1) or a water/formic acid/methanol gradient (method 2).
Axitinib and the internal standard (IS; axitinib-D3 for method 1
and pazopanib for method 2) were separated on an YMC-Pack Pro C4
column (50.times.3.0 mm I.D.; method 1) or a Phenomenex Luna C18
column (method 2) and quantitated using ESI selective reaction
monitoring mode with a total run time of approximately 6 min. For
quantification, the peak area of axitinib (m/z 387.2 to 356.0) and
the IS (m/z 390.2 to 356.0 for axitinib-D3 and m/z 438.2 to 357.1
for pazopanib) were determined and compared to a standard curve,
which showed linear behavior in the desired concentration range and
a correlation coefficient (r.sup.2) of >0.99. The LLOQ was 0.100
ng/mL.
Results: Determination of Axitinib in Plasma
[0641] The axitinib concentration in plasma and serum was
determined at indicated time-points in the different groups (Table
11). Determined concentrations were below the lower limit of
quantitation (LLOQ) during the duration of the studies for all
groups independent of the axitinib dose (ranging from 109 to 290
.mu.g per eye), demonstrating that the systemic exposure to
axitinib was near absent even for a total dose as high as 580 .mu.g
axitinib (290 .mu.g axitinib per eye adding up to a total of 580
.mu.g per rabbit). This further underlines safety of the implants
even for higher doses.
Results: Determination of Axitinib in Ocular Tissues
[0642] After hydrogel degradation, undissolved axitinib was
observed to form a localized structure continuing to release
axitinib (cf. Examples 3.2 to 3.4). These undissolved axitinib
particles may create erroneously high concentrations in tissue
samples due to preferential dissolution in the organic solvent used
for extraction prior to LC-MS/MS analysis. Therefore, it might have
been possible that tissue concentrations of axitinib after hydrogel
degradation were elevated due the presence of undissolved axitinib
particles contaminating the tissue samples due to either migration
near tissues or contamination during tissue dissection. The
solubility of axitinib in biorelevant media (PBS, pH 7.2 at
37.degree. C.; Lorget et al., 2016; Characterization of the pH and
temperature in the rabbit, pig, and monkey eye: key parameters for
the development of long-acting delivery ocular strategies.
Molecular pharmaceutics, 13(9), pp. 2891-2896) was determined to be
approximately 0.5 .mu.g/mL and any tissue values markedly higher
than this potentially indicated either tissue accumulation and/or
dissolution of axitinib particles in the organic solvent during
extraction. However, in general, measured ocular tissue levels of
axitinib correlated well with the visual presence or absence based
on IR imaging (FIGS. 7A, 9, and 10).
[0643] The aim of the study was to demonstrate axitinib
concentrations in the desired target tissues (choroid/RPE, retina,
and vitreous humor) well above the IC50 for the targeted tyrosine
kinase receptors (Gross-Goupil et al., Clinical Medicine Insights:
Oncology, 2013, 7:269-277) and above the half maximal effective
concentration (EC50) of free axitinib for inhibition of ocular
angiogenesis in a neonatal rat model as investigated in support of
INLYTA.RTM. (INLYTA.RTM. AusPAR 2013, NDA 202324; Table 12) for all
doses administered in order to validate efficient drug release.
TABLE-US-00014 TABLE 12 IC.sub.50 values of axitinib for binding to
vascular endothelial growth factor receptor 2 (VEGFR2),
platelet-derived growth factor receptor .beta. (PDGFR-.beta.), and
stem cell growth factor receptor/type III receptor tyrosine kinase
(c-Kit), as well as EC.sub.50 value of axitinib for inhibition of
ocular angiogenesis in a rat model. EC.sub.50 IC.sub.50 Rat Ocular
VEGFR2 PDGFR-.beta. c-Kit Angiogenesis Model 0.08 ng/mL 0.62 ng/mL
0.66 ng/mL 0.19 ng/mL (0.2 nM) (1.6 nM) (1.7 nM)
Ocular Tissue Distribution in Group 1 (1 Implant, 109 .mu.g
Axitinib)
[0644] Ocular tissue concentrations for indicated time points are
presented in Table 13.
TABLE-US-00015 TABLE 13 Ocular tissue distribution of axitinib
released from 1 implant with an axitinib dose of 109 .mu.g
axitinib. Axitinib concentrations in AH, VH (soluble part), retina,
and choroid/RPE are presented in dependence of the analysis
time-points as average (mean) including standard deviation,
coefficient of variation (CV) as well as the confidence interval
(CI) of the mean. In addition, minimum, median, and maximum values
for each data point are presented. Time N Std 95% Tissue Months
Eyes Average Min Median Max Dev CV CI AH 1 day 4 0.5 0.0 0.5 0.9
0.4 75% 0.4 (ng/mL) 1.5 3 2.7 0.8 1.5 5.9 2.8 102% 3.1 3 3 1.0 0.4
0.5 2.0 0.9 89% 1.0 4.5 4 0.7 0.6 0.7 1.0 0.2 23% 0.2 6 4 0.2 0.0
0.2 0.6 0.3 112% 0.2 7.5 3 0.0 0.0 0.0 0.0 0.0 n.a. n.a. 9 3 0.0
0.0 0.0 0.1 0.1 173% 0.1 VH 1 day 4 93.2 25.6 32.6 282.0 125.9 135%
123.4 (ng/mL) 1.5 3 23.1 12.9 15.1 41.3 15.8 68% 17.9 3 3 52.1 20.3
26.0 110.0 50.2 96% 56.8 4.5 4 115.8 58.4 89.8 225.0 77.6 67% 76.0
6 4 296.0 85.0 264.0 571.0 209.8 71% 205.6 7.5 3 184.9 2.9 21.7
530.0 299.0 162% 338.4 9 3 30.0 2.9 30.8 56.2 26.7 89% 30.2 Retina
1 day 4 184.7 116.0 147.4 328.1 97.7 53% 95.7 (ng/g) 1.5 3 165.5
69.0 169.9 257.6 94.4 57% 106.8 3 3 176.8 120.2 203.3 207.0 49.1
28% 55.5 4.5 4 271.8 153.0 206.0 522.1 170.3 63% 166.9 6 4 150.0
18.8 147.1 287.0 120.7 80% 118.2 7.5 3 15.3 13.6 14.6 17.7 2.1 14%
2.4 9 3 13.6 9.6 10.3 20.8 6.3 46% 7.1 Choroid/RPE 1 day 4 124.3
78.5 119.6 179.6 48.4 39% 47.5 (ng/g) 1.5 3 256.6 128.1 278.7 363.0
119.0 46% 134.7 3 3 328.2 96.6 306.5 581.6 243.2 74% 275.2 4.5 4
283.3 188.8 232.4 479.5 133.1 47% 130.5 6 4 95.0 52.0 98.4 131.0
32.6 34% 31.9 9 3 34.8 15.2 22.8 66.3 27.6 79% 31.2
[0645] Concentrations of axitinib in AH samples over the study
duration were considered low relative to the concentrations
observed in the VH, retina and choroid indicating a low level of
axitinib migration towards the anterior chamber from the posterior
chamber.
[0646] Median axitinib concentrations of soluble axitinib in VH
samples over the study duration were maximal (264.0 ng/mL) at 6
months. Individual samples ranged from a minimum of 2.9 ng/mL (7.5
and 9 months) to a maximum of 571.0 ng/mL (6 months). Maximum
values were similar to the solubility limit of axitinib in
biorelevant media, verifying that no undissolved axitinib disturbed
the measurements.
[0647] Median axitinib concentrations in the retina were similar
from day 1 (147.4 ng/g) through 6 months (147.1 ng/g) prior to a
noted decrease down to 14.6 ng/g at 7.5 months. This indicates
rapid and sustained transport of axitinib to the targeted retina
tissues from the implant within 1 day of administration through
approximately 6 months. Axitinib concentrations decreased
approximately 10-fold from 6 to 7.5 months in the retinal tissue
samples (147.1 to 14.6 ng/g). The average median axitinib
concentration through 6 months was 175 ng/g in the retina which was
well above the IC50 values for VEGFR2, PDGFR-.beta. and c-Kit
(2184, 282 and 265-fold, respectively) and therefore at
concentrations expected to inhibit neovascularization.
[0648] Median axitinib concentrations in the choroid/RPE were
similar from day 1 (119.6 ng/g) through 6 months (98.4 ng/g). This
indicates rapid and sustained transport of axitinib to the tissues
in the back of the eye by the implant within 1 day of
administration through approximately 6 months. Axitinib
concentrations decreased approximately 3-fold from 6 to 7.5 months
in the choroid/RPE tissue samples (98.4 to 33.3 ng/g). The average
median axitinib concentration through 6 months was 207 ng/g in the
choroid/RPE which was well above the IC50 values for VEGFR2,
PDGFR-.beta. and c-Kit (2589, 334 and 314-fold, respectively) and
therefore at concentrations expected to inhibit
neovascularization.
Ocular Tissue Distribution in Group 2 (1 Implant, 227 .mu.g
Axitinib)
[0649] Ocular tissue concentrations for indicated time points are
presented in Table 14.
TABLE-US-00016 TABLE 14 Ocular tissue distribution of axitinib
released from 1 implant with an axitinib dose of 227 .mu.g
axitinib. Axitinib concentrations in AH, VH (soluble part), retina,
and choroid/RPE are presented in dependence of the analysis
time-points as average (mean) including standard deviation,
coefficient of variation (CV) as well as the confidence interval
(CI) of the mean. In addition, minimum, median, and maximum values
for each data point are presented. N CV 95% Tissue Months Eyes
Average Min Median Max Std Dev % CI AH 1 12 8.2 0.0 0.0 69.9 20.4
247 11.5 (ng/mL) 3 18 0.0 0.0 0.0 0.4 0.1 424 0.0 6 12 0.0 0.0 0.0
0.1 0.0 123 0.0 7 6 0.0 0.0 0.0 0.1 0.0 93 0.0 VH 1 12 4829 33 327
36400 11113 230 6288 (ng/mL) 3 18 36430 48 614 610984 143547 394
66314 6 12 9765 55 5255 34355 10256 105 5803 7 6 8667 61 2105 41000
15971 184 12779 Retina 1 12 852 124 315 5080 1415 166 801 (ng/g) 3
18 1466 124 378 13990 3259 222 1505 6 12 21152 228 4957 154000
43428 205 24571 7 6 54121 131 13520 264000 103849 192 83095
Choroid/ 1 12 753 131 332 4920 1352 179 765 RPE 3 16 7214 0 240
60800 17708 245 8677 (ng/g) 6 12 1918 23 232 10100 3201 167 1811 7
6 3497 0 1772 10400 4265 122 3413
[0650] Axitinib concentrations were low in the AH with median
values of 0.0 ng/mL through study completion (7 months) indicating
little migration of axitinib from the posterior chamber to the
anterior chamber.
[0651] The axitinib concentration in the VH represents the soluble
axitinib that was dissolved in the VH. The median values at 1 and 3
months, prior to hydrogel degradation, were similar to the
determined solubility limit of axitinib in in PBS, pH 7.2 at
37.degree. C. (0.4 to 0.5 .mu.g/mL). The high median values at 6
and 7 months likely reflected contamination of VH samples with
undissolved axitinib particles that were solubilized during
extraction.
[0652] The median axitinib concentrations at 1 and 3 months in the
retina were similar to the solubility limit of axitinib. The
average median axitinib concentration over the first three months
was 341 ng/g in the retina which was well above the IC50 values for
VEGFR2, PDGFR-.beta. and c-Kit (4264, 569 and 487-fold,
respectively) and therefore at concentrations expected to inhibit
neovascularization. Similarly to the VH values, the median values
at 6 and 7 months likely reflected contamination of retina samples
with undissolved axitinib particles that were solubilized during
extraction.
[0653] The median axitinib concentrations at 1, 3 and 6 months in
the choroid/RPE tissue were similar to the solubility of axitinib.
The average median axitinib concentration over the first six months
was 274 ng/g in the choroid/RPE which was well above the IC50
values for VEGFR2, PDGFR-.beta. and c-Kit (3426, 457 and 391-fold,
respectively) and therefore at concentrations expected to inhibit
neovascularization. Similarly to VH and retina values, the median
values at 7 months likely reflected contamination of choroid
samples with undissolved axitinib particles that were solubilized
during extraction.
[0654] Although the axitinib concentrations at 6 and/or 7 months
likely reflected contamination with undissolved axitinib, it was
clearly demonstrated that the implant site provided a sustained
release of axitinib over the duration of the study.
Ocular Tissue Distribution in Groups 3 and 4 (2 Implants, Total
Dose of 290 .mu.g Axitinib with or without Avastin.RTM.)
[0655] Ocular tissue concentrations for indicated time points are
presented in Table 15.
TABLE-US-00017 TABLE 15 Ocular tissue distribution of axitinib
released from 2 implants with a total axitinib dose of 290 .mu.g
axitinib either without (group 3) or with (group 4) Avastin .RTM..
Axitinib concentrations in AH, VH (soluble part), retina, and
choroid/RPE are presented in dependence of the analysis time-points
as average (mean) including standard deviation, coefficient of
variation (CV) as well as the confidence interval (CI) of the mean.
In addition, minimum, median, and maximum values for each data
point are presented. (G = group; Av. = Average) Time N 95% Tissue G
Months Eyes Av. Min Median Max SD CV % CI AH 3 0.5 6 0.2 0.0 0.1
0.6 0.2 96 0.2 (ng/mL) 1 6 0.1 0.0 0.0 0.1 0.1 110 0.0 3 6 0.1 0.0
0.0 0.2 0.1 118 0.1 6 6 0.0 0.0 0.0 0.2 0.1 150 0.1 9 2 0.1 0.1 0.1
0.2 0.1 40 0.1 38 2 2.4 0.0 2.4 4.8 3.4 141 4.7 4 0.5 6 0.8 0.3 0.6
2.1 0.7 88 0.5 1 6 0.1 0.0 0.1 0.4 0.2 110 0.1 3 6 0.1 0.0 0.0 0.2
0.1 127 0.1 6 6 0.2 0.0 0.2 0.3 0.1 86 0.1 9 2 0.2 0.2 0.2 0.2 0.0
2 0.0 38 2 0.2 0.0 0.2 0.4 0.3 141 0.4 VH 3 0.5 6 642 149 553 1390
412 64 330 (ng/mL) 1 6 95 22 71 242 86 90 68 3 6 1869 50 277 6310
2720 146 2176 6 6 41 26 40 56 13 32 10 9 2 76 125 198 271 103 136
143 38 2 2 0 2 3 2 141 3 4 0.5 6 361 51 328 710 287 80 230 1 6 232
61 170 705 240 103 192 3 6 1959 33 672 5370 2517 128 2014 6 6 79 32
48 173 62 79 50 9 2 53 20 78 135 81 152 112 38 2 29 4 29 54 35 124
49 Retina 3 0.5 6 185 5 94 688 257 139 205 (ng/g) 1 6 240 40 99 622
261 109 209 3 6 9288 175 369 51000 20479 220 16386 6 6 1126 73 623
4190 1567 139 1254 9 2 80 52 183 313 184 232 256 38 2 28 0 28 55 39
141 54 4 0.5 5 118 39 91 302 106 90 93 1 6 205 70 144 448 153 75
123 3 6 6186 189 688 33700 13492 218 10796 6 6 4762 954 4255 10500
3299 69 2639 9 2 2068 136 4108 8080 5617 272 7785 38 2 28 21 28 36
11 38 15 Choroid/ 3 0.5 6 237 90 192 434 153 65 122 RPE 1 6 1103 48
114 5700 2260 205 1808 (ng/g) 3 6 4631 76 656 16600 6926 150 5542 6
6 17582 139 5940 81500 31603 180 25287 9 2 27748 335 83168 166000
117143 422 162349 38 2 19 0 19 39 27 141 38 4 0.5 6 1004 37 210
4940 1937 193 1550 1 6 2081 87 1608 5360 2112 101 1690 3 6 8399 363
6010 20300 8523 101 6820 6 6 17673 6740 11800 49000 15651 89 12523
9 2 7224 5080 14390 23700 13166 182 18247 38 2 57 17 57 98 58 100
80
[0656] An Avastin.RTM. dose of 1.25 mg has a half-life of 6.6 days
in rabbits (Sinapis et al., 2011; Pharmacokinetics of intravitreal
bevacizumab (Avastin.RTM.) in rabbits. Clinical ophthalmology
(Auckland, NZ), 5, p. 697) and by 1 month the mass remaining
approximates 0.05 mg. In line with that, the earliest time-point of
0.5 months demonstrated no obvious difference in ocular tissue
concentrations between groups 3 and 4 indicating similar drug
release when Avastin.RTM. concentration would be expected to be
highest in the VH in the rabbit model.
[0657] Axitinib concentrations in both groups were low in the AH
with median values of 0.2 ng/mL or less through study completion
indicating little migration of axitinib from the posterior chamber
to the anterior chamber. With the exception of one value at 38
months, the others were <1 ng/mL for the study duration.
[0658] The axitinib concentration in the VH is the soluble axitinib
that is dissolved in the VH. Median maximal concentrations in the
VH were 553 ng/mL in group 3 and 672 ng/mL in group 4. These values
were similar to the determined solubility limit of axitinib in
biorelevant media. Median concentrations through 9 months
demonstrated sustained release of axitinib from the implants in
both groups. Axitinib was detected in the VH even at 38 months.
[0659] In group 3, the axitinib median concentrations in the retina
tissue were maximal at 6 months (623 ng/g) and ranged from 94 to
623 ng/g between 0.5 to 9 months. Concentrations were less (28
ng/g) at 38 months, but still at a biologically effective
concentration. The average median axitinib concentration over the
first three months was 184 ng/g in the retina which was well above
the IC50 values for VEGFR2, PDGFR-B and c-Kit (2300, 307 and
263-fold, respectively) and therefore at concentrations expected to
inhibit neovascularization. In group 4, the values were comparable
to group 3 through 3 months, but levels were higher at 6 and 9
months and likely reflected contamination with undissolved axitinib
particles that were solubilized during extraction. The retina
tissue axitinib concentrations at 38 months were comparable between
groups 2 and 3.
[0660] In group 3, the average median axitinib concentration over
the first three months was 231 ng/g in the choroid/RPE tissue which
was well above the IC50 values for VEGFR2, PDGFR-B and c-Kit (2888,
386 and 330-fold, respectively) and therefore at concentrations
expected to inhibit neovascularization. The median values at 6 and
9 months likely reflected contamination with undissolved axitinib
particles that were solubilized during extraction. Concentrations
of axitinib in the choroid/RPE were less (19 ng/g) at 38 months,
but still at biologically effective concentration. In group 4,
axitinib concentrations in the choroid/RPE were similar compared to
group 3 at 0.5 months but were much higher at the later
time-points. Considering the broad range seen between the minimum
and maximum sample concentrations within each time-point, the
higher values likely reflected contamination with undissolved
axitinib particles that were solubilized during extraction.
Summary of the Ocular Distribution Data
[0661] Table 16 gives an overview of median axitinib concentrations
observed in the different tissues in all four groups in Dutch
Belted rabbits.
TABLE-US-00018 TABLE 16 Axitinib concentration measured in samples
from aqueous humor (AH), vitreous humor (VH), retina, and
choroid/RPE dependent on the axitinib dose (median value). Axitinib
concentration (ng/mL or ng/g, respectively) was measured at
indicated time points for the different groups using LC-MS/MS.
Group 1 Group 2 Group 3 Group 4 1 Implant 1 Implant 2 Implants 2
Implants + Avastin (109 .mu.g axitinib) (227 .mu.g axitinib) (290
.mu.g axitinib) (290 .mu.g axitinib) Time Time Time Time Tissue
(months) Median (months) Median (months) Median (months) Median AH
1 day 0.5 1 0.0 0.5 0.1 0.5 0.6 (ng/mL) 1.5 1.5 3 0.0 1 0.0 1 0.1 3
0.5 6 0.0 3 0.0 3 0.0 4.5 0.7 7 0.0 6 0.0 6 0.2 6 0.2 -- -- 9 0.1 9
0.2 7.5 0.0 -- -- 38 2.4 38 0.2 9 0.0 -- -- -- -- -- -- VH 1 day 33
1 327 0.5 553 0.5 328 (ng/mL) 1.5 15 3 614 1 71 1 170 3 26 6 5255 3
277 3 672 4.5 90 7 2105 6 40 6 48 6 264 -- -- 9 198 9 78 7.5 22 --
-- 38 2 38 29 9 31 -- -- -- -- -- -- Retina 1 day 147 1 315 0.5 94
0.5 91 (ng/g) 1.5 170 3 378 1 99 1 144 3 203 6 4957 3 369 3 688 4.5
206 7 13520 6 623 6 4255 6 147 -- -- 9 183 9 4108 7.5 15 -- -- 38
28 38 28 9 10 -- -- -- -- -- -- Choroid/ 1 day 120 1 332 0.5 192
0.5 210 RFT 1.5 279 3 240 1 114 1 1608 (ng/g) 3 307 6 232 3 656 3
6010 4.5 232 7 1772 6 5940 6 11800 6 98 -- -- 9 83168 9 14390 7.5
33 -- -- 38 19 38 57 9 23 -- -- -- -- -- --
[0662] There was a dose-related increase in axitinib concentrations
in the vitreous humor tissues for the mid (227 .mu.g) and high dose
(290 .mu.g) compared to the low dose (109 .mu.g). There was no
dose-related difference in the targeted tissues of the retina and
choroid prior to hydrogel degradation. In addition,
co-administration of Avastin.RTM. in group 4 did not change drug
release when compared to group 3. Even after 38 months, axitinib
was present at doses above the IC50 and EC50 in the VH, retina, and
choroid/RPE demonstrating sustained persistence. Axitinib was
either not detected in the aqueous humor or was present only at low
concentrations for all dose strengths through the duration of the
studies indicating a low level of axitinib migration towards the
anterior chamber from the posterior chamber were the implants are
localized.
Results: Axitinib Release Rate
[0663] In addition, also non-soluble axitinib in VH containing the
implant was assessed by LC-MS/MS analysis to determine the
remaining amount of axitinib at sacrifice time points. The axitinib
dose at the time of administration was determined by averaging
values from ten implants spiked into ten bovine VH samples.
[0664] In the low dose group (group 1, 109 .mu.g axitinib) and
intermediate dose group (group 2, 227 .mu.g axitinib), non-soluble
axitinib in VH containing the implant was assessed by LC-MS/MS
analysis to determine the remaining amount of axitinib at sacrifice
time points. The remaining amount was then compared to the initial
dose and the in vivo release rate over time was calculated. The
mean amount of axitinib released from the implant over 6 months in
rabbits was estimated to be 0.52 .mu.g/day. Following hydrogel
degradation, the rate of release appears to slow down as the
axitinib forms a localized structure. However, released axitinib
levels were still sufficient to inhibit vascular leakage (cf.
Example 3.4).
Example 3.6: Acute Exposure to Axitinib Bolus Dose
[0665] In order to test acute exposure to axitinib particles, an
intravitreal, bilateral bolus dose of a 600 .mu.g (1.2%) suspension
of axitinib in ProVisc.RTM. (Alcon; 1% 2000 kDa sodium hyaluronate)
was administered via a 50 .mu.L injection using a 27 G thin wall
needle syringe to Dutch belt rabbits (n=3 animals, 6 eyes).
[0666] At 1 month, rabbits were sacrificed and whole eyes were
prepared for histopathological analysis. The eyes were fixed,
sectioned vertically in 12 equal parts, stained with hematoxylin
and eosin (H&E) and examined by a board certified veterinary
pathologist. Histopathology assessments at each time point included
vitreous, retinal, scleral, or episcleral inflammation, retinal
disruption and fibrosis around the injected area. Tissues were
scored on a semi-quantitative scale from 0-5 for any abnormalities,
where 0 denotes no change (normal), 1 denotes rare foci of change
(minimal), 2 denotes mild diffuse change or more pronounced focal
change, 3 denotes moderate diffuse change, 4 denotes marked diffuse
change and 5 denotes severe diffuse change.
[0667] IOPs determined weekly remained within the normal range.
Intravitreal bolus dosing of 600 .mu.g of axitinib was generally
tolerable (Table 17). No gross lesions were noted in any eyes.
Minimal histiocytic and multinucleated giant cell inflammation was
observed around the axitinib injection site. Mild focal retinal
disruptions were observed in two eyes in proximity to the puncture
location and considered procedure related. Minimal retinal
disruption with a few macrophages in the photoreceptor layer was
observed in 1 of 6 eyes. Minimal retinal vacuolization was observed
in numerous sections from 4 of 6 eyes. Minimal to mild chronic
subcorneal inflammation was observed in 4 of 6 eyes.
TABLE-US-00019 TABLE 17 Axitinib bolus histopathological study
results. Results were scored on a scale of 0-5, where 0 denotes no
change (normal), 1 denotes rare foci of change (minimal), 2 denotes
mild diffuse change or more pronounced focal change, 3 denotes
moderate diffuse change, 4 denotes marked diffuse change and 5
denotes severe diffuse change. Results are presented as mean and
standard deviation (SD). Vitreous Retinal, Scleral, or Fibrosis
Chronic Retinal Retinal Chamber Episcleral Around the Subcorneal
Result Disruption Vacuolization Inflammation Inflammation Article
Inflammation Mean (SD) 0.10 (0.11) 0.50 (0.46) 0.23 (0.21) 0.03
(0.05) 0.00 (0.00) 0.28 (0.38)
[0668] In summary, the bolus injection was well-tolerated and safe.
The injected dose led to a higher acute localized axitinib dose per
compartmental volume in rabbit eyes (1.3 mL/eye) as it would have
led to in a human eye (4.5 mL/eye).
Example 4: Evaluation of Axitinib Implants in Beagle Dogs
[0669] In order to study the axitinib release from the implants in
beagle dogs, 12 dogs received each one implant per eye
(bilaterally) with 109 .mu.g axitinib via intravitreal injection
using a 27 G ultra-thin wall needle to administer the implant.
Formulation and dimensions of the implants injected are presented
in Table 6 (implant type #5).
[0670] Prior to implant administration, animals were anesthetized
with an intramuscular injection of ketamine hydrochloride (20
mg/kg) and xylazine (5 mg/kg). Eyes and the surrounding area were
cleaned with a 5% Betadine solution and rinsed with balanced salt
solution (BSS). One to two drops of topical proparacaine
hydrochloride anesthetic (0.5%) was applied. The eye was draped,
and a sterile wire speculum was placed to retract the eyelids. The
injection needle was placed approximately 3 to 5 mm away from the
limbus and deployed in a single stroke.
[0671] At predetermined sacrifice time points (3 animals each at
1.5, 3, 4.5, and 6 months post implant administration,
respectively) the eyes were collected, flash frozen, and then
dissected and weighed for the target tissues of the choroid,
retina, vitreous humor and aqueous humor. Plasma was additionally
collected at the selected time points. Axitinib concentrations were
assessed in AH, VH (soluble axitinib), choroid/RPE, and retina, as
well as in plasma. In addition, also non-soluble axitinib in VH
containing the implant was assessed by LC-MS/MS analysis to
determine the remaining amount of axitinib at sacrifice time points
(methods described under Example 3.5).
[0672] All values in plasma were reported as below the LLOQ (0.05
ng/mL for both isomers) indicating near absent systemic exposure to
axitinib in beagle dogs following implant administration (total
administered dose of 218 .mu.g).
[0673] Pharmacokinetic data of axitinib concentrations in the
target tissues over the study duration are presented in Table 18.
Concentrations of axitinib in beagle AH samples over 4.5 months
were considered low relative to the concentrations observed in the
VH, retina and choroid indicating a low level of axitinib migration
towards the anterior chamber from the posterior chamber prior to
hydrogel degradation. Axitinib was present at higher concentrations
in the AH at 6 months (after hydrogel degradation). This may have
been due to migration of undissolved axitinib particles released
from the degraded hydrogel towards the anterior chamber from the
posterior chamber or due to sample contamination of the AH by VH
during tissue dissection. High axitinib concentrations in the AH
were never observed in any of the rabbit studies.
[0674] Median axitinib concentrations in the VH were similar over
the study duration (range from 11.9 to 27.1 ng/mL). These values
were similar to that observed in the monkey study at a similar dose
(138 .mu.g; cf. Example 5).
[0675] Median axitinib concentrations in the retina were similar
over the study duration (range from 15.4 to 31.0 ng/mL) indicating
continuous sustained delivery of axitinib from the implant to
retina tissues. The average median axitinib concentration over six
months was 23 ng/g in the retina which was well above the IC50
values for VEGFR2, PDGFR-.beta. and c-Kit (288, 37 and 35-fold,
respectively) and therefore at concentrations expected to inhibit
neovascularization. In addition, this concentration was 121-fold
higher than the EC50 determined for free axitinib in the ocular
angiogenesis neonatal rat model.
[0676] Median axitinib concentrations in the choroid/RPE were
similar over the study duration (range from 16.2 to 39.8 ng/g)
indicating sustained delivery of axitinib from the implant to the
choroid tissues through study completion. The average median
axitinib concentration over six months was 31 ng/g in the
choroid/RPE which was well above the IC50 values for VEGFR2,
PDGFR-.beta. and c-Kit (388, 50 and 47-fold, respectively) and
therefore at concentrations expected to inhibit neovascularization.
In addition, this concentration was 163-fold higher than the EC50
determined for free axitinib in the ocular angiogenesis neonatal
rat model.
TABLE-US-00020 TABLE 18 Pharmacokinetic study results in beagle
dogs. Axitinib concentrations in AH, VH (soluble part), retina, and
choroid/RPE are presented in dependence of the analysis time-points
as average (mean) including standard deviation, coefficient of
variation (CV) as well as the confidence interval (CI) of the mean.
In addition, minimum, median, and maximum values for each data
point are presented. Time N Std 95% Tissue Months Eyes Average Min
Median Max Dev CV CI AH 1.5 4 2.8 0.4 3.1 4.6 2.1 76 2.0 (ng/mL) 3
6 1.2 0.1 0.9 3.2 1.1 87 0.8 4.5 5 0.6 0.5 0.6 0.9 0.1 22 0.1 6 6
66.4 0.5 14.5 228.0 94.9 143 76.0 VH 1.5 4 26.8 20.7 27.1 32.5 5.5
20 5.4 (ng/mL) 3 6 19.4 16.5 18.4 23.3 2.5 13 2.0 4.5 5 10.1 1.8
11.9 18.1 6.5 64 5.7 6 6 33.6 0.9 17.2 84.3 36.3 108 29.1 Retina
1.5 4 27.6 22.2 23.9 40.6 8.7 32% 8.5 (ng/g) 3 6 30.8 18.7 31.0
39.2 7.8 25% 6.2 4.5 5 52.3 8.6 20.4 134.0 56.5 108% 49.5 6 6 16.2
1.9 15.4 35.2 11.4 70% 9.1 Choroid/RPE 1.5 4 35.7 13.5 29.3 70.8
24.6 69% 24.1 (ng/g) 3 6 29.5 8.3 16.2 87.8 29.9 101% 24.0 4.5 5
62.1 9.5 39.8 126.0 48.0 77% 42.1 6 6 72.9 5.9 38.2 250.0 90.6 124%
72.5
[0677] The mean amount of axitinib released from the implant over 6
months in beagle dogs was estimated to be approximately 0.52
.mu.g/day (Table 19), similar to the release rates seen in rabbits
with the same dose (cf. Example 3.5). The axitinib dose at the time
of administration was determined by averaging values from ten
implants spiked into ten bovine VH samples.
TABLE-US-00021 TABLE 19 Non-soluble axitinib in VH containing the
implant. Baseline values refer to the axitinib amount in the
implants prior to administration. Time Average Min Median Max. Std
Dev 95% Months N (.mu.g) (.mu.g) (.mu.g) (.mu.g) (.mu.g) CV CI
Baseline 10 109 95 110 119 7 6% 4 1.5 4 75 72 76 77 2 3% 2 3 6 50
28 54 59 11 23% 9 4.5 5 42 0 49 67 26 62% 23 6 6 15 0 13 39 16 104%
13
Example 5: Evaluation of Axitinib Implants in Non-Human
Primates
[0678] In order to study safety and drug release in African green
monkeys, animals received one implant in either the right or left
eye (for drug release studies) or bilaterally (for safety and
tolerability studies) via intravitreal injection using a 27 G
ultra-thin wall needle, the implant comprising an axitinib dose of
138 .mu.g. Formulation and dimensions of the implants injected are
presented in Table 6 (implant type #4).
[0679] Prior to implant administration, animals were anesthetized
with an intramuscular injection of ketamine hydrochloride (20
mg/kg) and xylazine (5 mg/kg). Eyes and the surrounding area were
cleaned with a 5% Betadine solution and rinsed with balanced salt
solution (BSS). One to two drops of topical proparacaine
hydrochloride anesthetic (0.5%) was applied. The eye was draped,
and a sterile wire speculum was placed to retract the eyelids. The
injection needle was placed approximately 3 to 5 mm away from the
limbus and deployed in a single stroke.
Drug Release
[0680] To evaluate drug release, 6 monkeys were sacrificed 3 months
after implant administration and the eyes were collected, flash
frozen, and then dissected and weighed for target tissues of the
choroid, retina, vitreous humor and aqueous humor. Serum was
additionally collected at the selected time point. Subsequent
analysis following axitinib extraction from tissues (where
necessary) and dilution was performed, followed by LC-MS/MS for the
determination of axitinib concentrations in the samples (methods
described under Example 3.5).
[0681] Pharmacokinetic data of median axitinib concentrations in
the target tissues is presented in Table 20. As observed for
rabbits and beagle dogs, axitinib concentrations in the AH were low
indicating little movement of axitinib from the posterior to the
anterior chamber in the monkey eye. Soluble axitinib concentrations
in the VH were low (12 ng/mL) compared to those observed in
rabbits, but they were similar to concentrations observed in beagle
dogs.
[0682] The average median axitinib concentration over the three
months was 39 ng/g in the retina which was well above the IC50
values for VEGFR2, PDGFR-13 and c-Kit (488, 63 and 59-fold,
respectively) and therefore at concentrations expected to inhibit
neovascularization. In addition, this concentration was 205-fold
higher than the half-maximal effective concentration (EC50=0.19
ng/mL) determined for free axitinib in the ocular angiogenesis
neonatal rat model.
[0683] The average median axitinib concentration over the three
months was 940 ng/g in the choroid/RPE tissue which was well above
the IC50 values for VEGFR2, PDGFR-13 and c-Kit (11750, 1516 and
1424-fold, respectively) and therefore at concentrations expected
to inhibit neovascularization. In addition, this concentration was
4947-fold higher than the EC50 determined for free axitinib in the
ocular angiogenesis neonatal rat model.
[0684] The choroid/RPE axitinib concentration at 3 months was
significantly higher in monkeys (940 ng/g) compared to rabbits
(240, 656, and 307 ng/g, respectively) and beagle dogs (16 ng/g).
As axitinib was found to bind to melanin in the uveal tract of the
eye in mice (INLYTA.RTM. support, NDA202324), this might be due to
an increased ocular melanin content in the central and peripheral
choroid/RPE compared to rabbits and beagles (Durairaj et al., 2012,
Intraocular distribution of melanin in human, monkey, rabbit,
minipig, and dog eyes. Experimental eye research, 98, pp. 23-27).
In addition, also varying vitreous volumes may have contributed to
differences observed in tissue concentrations (Dutch belted
rabbit=1.3 mL, beagle dog=2.2 mL, and African green monkey=2.4 mL;
Glogowski et al., 2012, Journal of ocular pharmacology and
therapeutics, 28 (3), pp. 290-298; Struble et al., 2014, Acta
Ophthalmologica, 92).
[0685] Moreover, the systemic exposure to axitinib in serum from
the implant was below the LLOQ (0.088 ng/mL for trans-axitinib and
0.012 ng/mL for cis-axitinib).
TABLE-US-00022 TABLE 20 Pharmacokinetic study results in African
green monkeys. Axitinib concentrations in AH, VH (soluble part),
retina, and choroid/RPE are presented in dependence of the analysis
time-points as average (mean) including standard deviation,
coefficient of variation (CV) as well as the confidence interval
(CI) of the mean. In addition, minimum, median, and maximum values
for each data point are presented. Time N Std 95% Tissue Months
Eyes Average Min Median Max Dev CV CI AH 3 6 0.47 0.00 0.48 0.76
0.28 59% 0.22 (ng/mL) VH 3 6 16 4 12 37 12 73% 9 (ng/mL) Retina 3 6
52 28 39 89 28 54% 22 (ng/g) Choroid/RPE 3 6 1107 568 940 1980 417
38% 193 (ng/g)
Safety and Tolerability
[0686] To evaluate safety and tolerability, the 6 monkeys were
monitored for 3 months post implant administration. Ocular
examination was performed via ophthalmic slit-lamp examination and
graded according to the modified Hackett-McDonald scoring system.
Ocular examination revealed no notable findings, including no
intraocular inflammation or retinal changes over the study
duration. No changes in IOP or pupil diameter occurred over the
study duration.
Conclusions from Pre-Clinical Animal Studies
[0687] In summary, pharmacokinetic results demonstrate levels of
axitinib in the relevant ocular tissues (VH, Retina, Choroid/RPE)
delivered from the implants significantly above the IC50 for
tyrosine kinases and the EC50 for inhibition of angiogenesis in a
rat model (Table 12) in all animals examined (dog, beagle, monkey)
over a duration of up to 38 months. In general, measured ocular
tissue levels of axitinib correlated with the visual presence or
absence of the implants and the drug in the posterior chamber based
on IR imaging. In contrast, axitinib concentrations in the AH were
either absent or very low compared to VH, retina, and choroid/RPE
verifying that only a low level of axitinib migration towards the
anterior chamber from the posterior chamber were the implants are
localized occurred in all three animal species. However, the drug
release in humans may differ from non-clinical studies due to
comparative differences between animals and humans with respect to
vitreous volumes, vitreous viscosities, and drug clearance rates
that directly relate to the surface area of the retinal pigment
epithelium (RPE) for small molecules.
[0688] All animal studies demonstrated that levels in plasma/serum
were below the LLOQ indicating near absent systemic exposure to
axitinib. Therefore, the plasma/serum levels resulting from
implants of the present application were much lower than serum
levels reported in the literature for INLYTA.RTM.. Because axitinib
has no subsequent distribution outside of the intraocular
compartment, any drug-drug interaction risk can be considered
minimal.
[0689] Imaging analysis by IR demonstrated visual biodegradation of
the hydrogel in the posterior chamber over time leading to complete
degradation after approximately 6 months. Axitinib drug particles
remaining at the former implant locations formed a monolithic
structure continuing to release axitinib at levels sufficient for
sustained inhibition of vascular leakage. Efficacy in suppression
of vascular leakage was demonstrated out to 6 and 21 months in
rabbit VEGF challenge studies. Co-administration of bevacizumab
resulted in an even more rapid inhibition of vascular leakage in
the first 3 months when compared to administration of the axitinib
implants alone.
[0690] Taken together, the data demonstrate that the axitinib
implants of the present invention are safe and well-tolerated as
well as show sufficient drug-release and good efficacy in rabbits,
dogs, and African green monkeys.
Example 6: Human Clinical Trials with Axitinib Implants
[0691] The axitinib implants of the present application were
examined in humans in a next step. The axitinib implants are
applied in order to reduce choroidal/retinal neovascularization and
exudation, decrease vascular permeability, decrease (or essentially
maintain or prevent a clinically significant increase of) central
subfield thickness, while in certain embodiments not impairing or
even improving visual acuity. As the implants provide sustained
release of axitinib and thus a prolonged provision of axitinib to
the vitreous humor and the surrounding tissue, treatment with the
implants of the present application reduces the burden on patients
and caregivers, as well as the risk of adverse effects associated
with frequent injections of anti-VEGF therapeutics.
[0692] Subjects with neovascular age-related macular degeneration
(wet AMD) who had retinal fluid were enrolled in an open-label,
dose-escalation study to evaluate safety, tolerability and efficacy
of the axitinib implants of the present invention in human
subjects. Patients were naive or non-naive to treat
Example 6.1: Formulations
[0693] Tables 21.1 and 21.2 give an overview of formulations and
dimensions of implants containing about 200 .mu.g and about 600
.mu.g axitinib, some of which are applied in human clinical trials
(or are planned or suitable to be applied in future human clinical
trials). The dimension of the implants in the dry state were
measured after the implants had been produced and had been dried
and just before they were loaded into the needles. The implants
remained in an inert glove box kept below 20 ppm of both oxygen and
moisture for at least about 7 days prior to packaging. The
dimensions of hydrated implants indicated in these tables were
measured after 24 hours in biorelevant media (PBS, pH 7.2 at
37.degree. C.).
[0694] Measurement of the implant dimensions (both in the dry and
in the wet state) were performed by a custom 3-camera Keyence
Inspection System. 2 Cameras were used to measure the diameter with
a tolerance of +0.002 mm (of all datapoints acquired, the average
(=mean) value is recorded), and 1 camera was used to measure the
length with a tolerance of +0.04 mm (of several datapoints, the
longest measured length is recorded).
TABLE-US-00023 TABLE 21.1 Formulation, configuration and dimensions
of an implant with an axitinib dose of about 200 .mu.g that was
used in the clinical studies reported in Example 6.3 and 6.4.
Implant type Implant #1 Formulation Axitinib 49.4% (% dry Dose (200
.mu.g) basis w/w) PEG Hydrogel 42.0% 4a20K PEG-SAZ 28% 8a20K
PEG-NH2 14% Sodium phosphate 8.6% Formulation Axitinib 7.5% (% wet
PEG Hydrogel 6.9% basis w/w) 4a20K PEG-SAZ 4.6% 8a20K PEG-NH2 2.3%
Sodium phosphate 1.5% WFI 84.1% Axitinib per final dry 12.1
.mu.g/mm length Approximate Implant 423 Mass (dose .mu.g/API %)
Configuration Stretching Method Dry (Stretch Factor) (4.5) Needle
Size 27G TW 1.25'' (0.27 mm ID) Injector/Syringe Implant Injector
Packaging Foil Pouches Sterilization Type Gamma Site Storage
Refrigerated Dimensions Dried Diameter 0.24 .+-. 0.013 mm Length
16.5 .+-. 0.26 mm Volume 0.75 .+-. 0.08 mm.sup.3 Implant Mass 0.45
mg Axitinib per volume 266.7 (.mu.g/mm.sup.3) Hydrated Diameter
0.75 mm Length 7.5 mm Ratio of diameter 3.13 (hydrated) to diameter
(dry) Ratio of length (dry) 2.20 to length (hydrated)
TABLE-US-00024 TABLE 21.2 Formulations, configurations and
dimensions of implants with axitinib doses of about 600 .mu.g.
Implant type Implant #2 Implant #3 Implant #4 Formulation Axitinib
49.8% 68.6% 68.6% (% dry Dose (600 .mu.g) (600 .mu.g) (600 .mu.g)
basis w/w) PEG Hydrogel 42.0% 26.0% 26.0% 4a20K PEG-SAZ 28% 17.4%
17.4% 8a20K PEG-NH2 14% 8.7% 8.7% Sodium phosphate 8.2% 5.4% 5.4%
Formulation Axitinib 12.0% 16.5% 16.5% (% wet PEG Hydrogel 6.3%
6.3% 6.3% basis w/w) 4a20K PEG-SAZ 4.2% 4.2% 4.2% 8a20K PEG-NH2
2.1% 2.1% 2.1% Sodium phosphate 1.3% 1.3% 1.3% WFI 80.4% 75.9%
75.9% Axitinib per final dry 71.4 .mu.g/mm 71.4 .mu.g/mm 81.1
.mu.g/mm length Approximate Implant 1205 875 875 Mass (dose ug/API
%) Configuration Stretching Method Wet Wet Wet (Stretch Factor)
(2.1) (2.1) (2.1) Needle Size 25G UTW 1'' 25G UTW 1'' 25G UTW 0.5''
(0.4 mm ID) (0.4 mm ID) (0.4 mm ID) Injector/Syringe Implant
Injector Implant Injector Implant Injector Packaging Foil Pouches
Foil Pouches Foil Pouches Sterilization Type Gamma Gamma Gamma Site
Storage Refrigerated Refrigerated Refrigerated Dimensions Dried
Diameter 0.36 mm 0.37 .+-. 0.014 mm 0.37 .+-. 0.008 mm Length 8.4
mm 8.4 .+-. 0.04 mm 7.4 .+-. 0.03 mm Volume 0.86 mm.sup.3 0.90 .+-.
0.07 mm.sup.3 0.81 .+-. 0.05 mm.sup.3 Implant Mass 1.20 mg 0.95
.+-. 0.04 mg 0.95 .+-. 0.01 mg Axitinib per volume 697.7 666.7
740.7 (.mu.g/mm.sup.3) Hydrated Diameter 0.7 mm 0.68 mm 0.77 mm
Length 10 mm 8.23 mm 6.8 mm Ratio of diameter 1.94 1.84 2.08
(hydrated) to diameter (dry) Ratio of length (dry) 0.84 1.02 1.09
to length (hydrated)
[0695] The 200 .mu.g implant of Table 21.1 and used in the clinical
study further described below was also investigated for axitinib
release in the in vitro real time and accelerated assays (assays as
described in Example 2). The in vitro real-time data suggest
complete axitinib release after 225 days, while accelerated release
is complete after around 2 weeks (FIG. 14).
Example 6.2: Details of Clinical Study
[0696] The clinical study using the 200 .mu.g implant (Implant #1
of Table 21.1 above) was conducted in accordance with the study
protocol, which is reproduced in the following (although the study
has already begun and parts of it have already been performed, and
the results are reported in Example 6.3 and 6.4 herein, as is
common for study protocols, the study protocol is nevertheless
written in the present and future tense). The implant referred to
in the study protocol as "OTX-TKI" is Implant #1 of Table 21.1,
above. Depending on the dose, one (dose of 200 .mu.g), two (dose of
400 .mu.g) or three (dose of 600 .mu.g) implants are administered
concurrently as described herein. Any abbreviations used in the
following study protocol as well as Appendices A to G mentioned
herein are provided at the end of the study protocol (i.e., at the
end of Example 6.2).
Study Objective
[0697] The primary study objective is to evaluate the safety,
tolerability and efficacy of OTX-TKI (axitinib implant) for
intravitreal use, in subjects who have neovascular age-related
macular degeneration (nvAMD).
Study Design
[0698] This is a multi-center, open label, dose escalation, Phase 1
safety study. This safety study will enroll approximately 26
subjects at approximately 5 sites in Australia. Three cohorts will
be evaluated during this study: 200 .mu.g (Cohort 1) and 400 .mu.g
(Cohort 2) dose groups followed by a third cohort (Cohort 3)
consisting of two different treatment groups designed to test
monotherapy (6 subjects receiving 600 .mu.g OTX-TKI) and
combination therapy with anti-VEGF (6 subjects treated with 400
.mu.g OTX-TKI along with a single anti-VEGF injection). Safety data
from subjects treated in Cohorts 1 and 2 will be evaluated by the
DSMC prior to the initiation of the next cohort. The study will
last approximately 9 months; there will be a screening/baseline
visit followed by the injection day visit, with approximately 10
additional visits (See Appendix A).
[0699] The screening visit (Visit 1) may take place up to 14 days
prior to the Injection Visit (Visit 2; Day 1). At Visit 2, subjects
will have the OTX-TKI implant(s) injected (for Cohort 3, injections
of the OTX-TKI implants and anti-VEGF may be spaced out over 1-4
weeks at the Investigator's discretion). Subjects will return for
follow-up visit 2-3 days later for post-operative evaluation at
Visit 3. Subjects will then return in approximately one week (Visit
4) and then again at approximately two weeks (Visit 5) for safety
evaluations. Following that, subjects will return for safety
evaluations on: Visit 6 (Month 1), Visit 7 (Month 2), Visit 8
(Month 3), Visit 9 (Month 4.5), Visit 10 (Month 6), Visit 11 (Month
7.5) and Visit 12 (Month 9) for final safety evaluations, and to be
discharged from the study. At the Investigator's discretion,
subjects who still have evidence of biological activity at Month 9
should be followed monthly until the CNV leakage has returned to
baseline levels or until the Investigator believes the subject is
clinically stable.
[0700] Cohort 1 is planned to comprise 6 subjects. They will each
receive one 200 .mu.g implant per eye which is estimated to provide
an approximate drug delivery of about 7 .mu.g per week.
[0701] Cohort 2 is planned to comprise 6 to 8 subjects. They will
each receive two 200 .mu.g implants per eye which together are
estimated to provide an approximate drug delivery of about 14 .mu.g
per week.
[0702] Cohort 3a (monotherapy) is planned to comprise 6 subjects.
They will each receive three 200 .mu.g implants per eye which
together are estimated to provide an approximate drug delivery of
about 21 .mu.g per week.
[0703] Cohort 3b (combination treatment therapy) is planned to
comprise 6 subjects. They will each receive two 200 .mu.g implants
per eye which together are estimated to provide an approximate drug
delivery of about 14 .mu.g per week plus a single dose of an
anti-VEGF agent.
[0704] Cohort 1 will be fully enrolled and all safety and
tolerability data of OTX-TKI for each subject (minimum follow up
data for two weeks) will be assessed prior to any subject entering
the next cohort. The same process will be repeated for Cohort 2.
Dose escalation to the next cohort will be based on the
recommendation of the DSMC and confirmed by the MM.
[0705] If one DLT is identified in Cohorts 1, 2, or 3a, enrollment
will continue until the cohort has been fully enrolled. If a second
DLT is seen in Cohorts 1, 2, or 3a, enrollment will stop. If a
second DLT is seen in Cohort 3a, enrollment in that cohort will
stop and the previous lower dose will be declared the MTD.
[0706] In addition to safety and tolerability evaluations, this
first clinical study will also determine if there is any evidence
of biological activity by assessing changes in central subfield
thickness (CSFT), FA and BCVA over time compared with baseline
evaluations.
[0707] Subjects can have only 1 eye treated with OTX-TKI. The
contralateral eye, if needed, will be treated at the Investigator's
discretion. This should be standard of care and in no case should
another investigational drug be used for the contralateral eye.
[0708] If both eyes are eligible, the eye with the worst BCVA will
be selected as the study eye. If both eyes are eligible and both
have the same BCVA then the Investigator will determine which eye
will be selected as the study eye.
Safety Outcome Measures
[0709] Safety will be assessed immediately following injection of
the implant. During the immediate post-injection time subjects will
be monitored for visual acuity and elevated IOP.
[0710] The safety outcome measures will include an assessment of:
[0711] Incidence of treatment emergent ocular adverse events [0712]
Incidence of treatment emergent systemic adverse events [0713]
Vital signs [0714] Ocular comfort score (to be assessed by
subjects) [0715] BCVA [0716] Change in ocular examination compared
to baseline assessment (e.g., slit lamp biomicroscopy, fundus
examination) [0717] Anterior chamber cell and flare score [0718]
Vitreous cell and haze score [0719] Clinically significant
increases in IOP [0720] Potential injection related complications
(e.g., endophthalmitis, retinal detachment, etc.) [0721] Growth or
development of geography atrophy [0722] Clinically significant
change in safety laboratory values [0723] Plasma sample for
pharmacokinetic analysis will be taken at Screening/Baseline Visit
(Visit 1), Day 1 (Visit 2), Day 3 (Visit 3), and Month 3 (Visit
8).
Efficacy Outcome Measures
[0724] Efficacy measures will be observed throughout the conduct of
the study. The efficacy outcome measures will include an assessment
of: [0725] Mean change in central subfield thickness (CSFT) from
baseline over time measured by SD-OCT at 6 months and all visits
[0726] Change in BCVA from baseline over time at 6 months and all
visits [0727] Clinically significant change in leakage determined
by FA and OCT-A [0728] A decrease in CSFT of .gtoreq.50 .mu.m at
each study visit compared to baseline through Month 9 [0729]
Absence of any SRF and IRF, both individually and together at each
study visit [0730] Need for rescue therapy
Subject Selection--Study Population
[0731] The subjects enrolled in this study will have a diagnosis of
primary subfoveal (active sub- or juxtafoveal CNV with leakage
involving the fovea) neovascularization (SFNV) secondary to AMD.
Subjects with predominantly classic, minimally classic or occult
lesions will all be included.
[0732] If both eyes qualify (i.e., all inclusion and exclusion
criteria are met) then the eye with the worse BCVA will be the
study eye. If both eyes qualify AND both eyes have the same BCVA,
then the Investigator will determine which eye will be selected as
the study eye.
Subject Selection--Inclusion Criteria
[0733] Individuals of either gender will be eligible for study
participation if they: [0734] 1. Are at least 50 years of age
[0735] 2. Are eligible for standard therapy [0736] 3. Have active
primary CNVM secondary to AMD, either newly diagnosed or previously
treated with documented response to anti-VEGF therapy in the study
eye [primary subfoveal CNV secondary to AMD including juxtafoveal
lesions that affect the fovea] documented by FA and SD-OCT [0737]
4. Have a lesion area <30.5 mm.sup.2 (12 disc areas) (measured
according to the protocol of the Macular Photocoagulation Study) in
the study eye [0738] 5. Have a total area of CNV that is
.gtoreq.50% of total lesion by Fluorescein angiography (FA) and
fundus photography in the study eye [0739] 6. Have presence of
foveal intraretinal or subretinal fluid with CSFT >300 .mu.m on
SD-OCT in the study eye [0740] 7. Have adequate ocular media and
adequate pupillary dilation in the study eye to permit good quality
fundus imaging [0741] 8. Have had an electrocardiogram within 12
weeks prior to Day 1 (day of injection) that shows no clinically
significant abnormalities [0742] 9. Are female who is
postmenopausal for at least 12 months prior to screening or
surgically sterile; or male or female of childbearing potential
willing to use two forms of adequate contraception from screening
until they exit the study [0743] 10. Are able and willing to comply
with all study requirements and visits [0744] 11. Have provided
written informed consent.
Subject Selection--Exclusion Criteria
[0745] Individuals are not eligible for study participation if
they: [0746] 1. Have monocular vision [0747] 2. Have a scar,
fibrosis or atrophy involving the center of the fovea that is
severe (mild fibrosis or atrophy is not exclusionary) in the study
eye [0748] 3. Have evidence of a scar or fibrosis of >50% of the
total lesion in the study eye [0749] 4. Have previous laser
photocoagulation to the center of the fovea in the study eye [0750]
5. Have history of intraocular surgery including cataract surgery
or keratorefractive surgery (LASIK, PRK, etc.) or another treatment
in the study eye within 3 months of screening [0751] 6. Aphakia in
the study eye [0752] 7. Have expectation of penetrating
keratoplasty, vitrectomy, cataract surgery, or LASIK or any other
intraocular surgery during the study period in the study eye [0753]
8. Have a history of vitreoretinal surgery (including vitrectomy)
or other ocular surgeries including scleral buckle or glaucoma
filtering/shunt surgery in the study eye. Prior laser treatment,
other than for treatment of CNV is allowed [0754] 9. Have a
presence of a disease other than NV (wet) AMD in the study eye that
could affect vision or safety assessments [0755] 10. Have a history
of significant ocular infection (bacterial, viral, or fungal)
within the previous 3 months, or history of herpetic ocular
diseases (including herpes simplex virus, varicella zoster or
cytomegalovirus retinitis) or toxoplasmosis gondii or
chronic/recurrent inflammatory eye disease (i.e., scleritis,
uveitis, corneal edema) in either eye [0756] 11. Have evidence of a
rhegmatogenous retinal detachment or visually significant
epiretinal membrane (severe ERM), or macular hole, or tear of the
retinal pigment epithelium (RPE) in the macula in the study eye
[0757] 12. Have proliferative diabetic retinopathy, branch retinal
vein occlusion or central retinal vein occlusion in the study eye
[0758] 13. Have a history of diabetic macular edema (DME) in the
study eye [0759] 14. Have a history of or presence of vitreous
hemorrhage in the study eye. Subject is still eligible if history
of past hemorrhagic PVD has resolved [0760] 15. Have advanced
glaucoma (uncontrolled IOP>25 mmHg despite treatment) or
glaucoma filtration surgery in the study eye [0761] 16. Have
pathologic myopia in the study eye [0762] 17. Have a spherical
equivalent of the refractive error in the study eye of >10
diopters of myopia [0763] 18. Have any prior treatment with
tyrosine kinase inhibitors [0764] 19. Have an ocular malignancy
including choroidal melanoma in either eye [0765] 20. Are receiving
concurrent treatment with medications known to be toxic to the
retina, lens or optic nerve (e.g., chlorpromazine, phenothiazines,
tamoxifen, etc.) [0766] 21. Have a need for chronic therapy with
systemic or topical ocular corticosteroids (a short course of <7
days, if needed during the study is permissible) or have known
allergy to fluorescein (e.g., bronchospasm, rash, etc.), or to any
component of the study products [0767] 22. Have symptomatic or
unstable coronary artery disease, angina, congestive heart failure,
or an arrhythmia requiring active medical management within the
last 30 days of the injection of the implant [0768] 23. Have
uncontrolled hypertension (defined as >160/100 mm Hg, despite
medical treatment) [0769] 24. Have a history of or presence of
uncontrolled systemic disease or a debilitating disease (e.g.,
uncontrolled diabetes). [0770] 25. Have had a myocardial infarction
or other cardiovascular event (e.g., stroke) within the previous 6
months [0771] 26. Have participated in any study involving an
investigational drug either in the U.S. or outside the U.S. within
the past 30 days [0772] 27. Are an employee of the site that is
directly involved in the management, administration, or support of
the study, or be an immediate family member of the same.
Study Data Collection--Study Schematic
[0773] The study Time and Event Schedule is presented in Appendix
A. Procedures for study Assessments can be found in Appendix B-G
herein at the end of the study protocol (i.e., at the end of
Example 6.2).
Study Observations and Procedures--Subject Screening and Informed
Consent
[0774] Potential eligibility will be determined prior to study
enrollment. The Investigator and study staff will determine the
subject's willingness and ability to meet the follow-up
requirements. If the subject desires to participate in the study,
written informed consent will be obtained prior to performance of
any study-specific examinations. Following completion of all the
screening and baseline evaluations a determination will be made by
the Investigator and study staff as to whether or not the subject
has met all the eligibility criteria. If the subject meets the
eligibility criteria and agrees to participate the subject will be
enrolled.
[0775] Once a subject qualifies for the study and has received the
OTX-TKI they must be followed to the end of the study period.
[0776] If the injection of the OTX-TKI implant is unsuccessful,
record the reason for injection failure on the CRF as an injection
failure and not as an AE.
[0777] Once the implant is placed in the vitreous the Investigator
should verify placement by indirect ophthalmoscopy. At the
discretion of the Investigator, images of the implant may be
obtained throughout the duration of the study.
[0778] If the injection of the OTX-TKI implant is unsuccessful, an
additional subject will be assigned to the study according to the
same cohort.
Study Observations and Procedures--Screen Failures
[0779] Subjects who have signed the Informed Consent Form, but are
determined to be ineligible during the screening assessments or at
the baseline visit but prior to assignment to a cohort will be
considered screen failures, will be withdrawn from the study, and
will not require additional study follow-up visits. The reason(s)
for the screen failure will be recorded in the CRF.
[0780] If subjects who fail eligibility criteria experience an AE
during Screening/Baseline, they will be followed until the AE is
resolved or stabilized.
Study Observations and Procedures--Subject Withdrawal
[0781] All subjects treated in the study will be required to adhere
to the follow-up schedule as described in this protocol.
[0782] Subjects may withdraw from the clinical study at any time
for any reason without jeopardy or prejudice and without
compromising their clinical care by the Investigator. The
Investigator also has the right to withdraw subjects from the trial
in the event of an intercurrent illness, AE, protocol violation
and/or administrative reason.
[0783] For any subject who withdraws their consent following
injection of OTX-TKI, to the extent possible, the reason(s) for
withdrawal will be documented on the End of Study CRF.
[0784] If the withdrawal from the study is a result of an AE, or
death, an AE Form will also be completed. If a subject is withdrawn
from the study as a result of an AE, every attempt should be made
by the Investigator to follow the subject until the AE has resolved
or stabilized.
[0785] Every attempt will be made to contact subjects who are
non-compliant or lost to follow-up and such attempts will be
documented in the subject's study record.
[0786] Subjects who withdraw from the study after receiving the
OTX-TKI (axitinib implant) for intravitreal use will not be
replaced.
Study Observations and Procedures--Product Malfunctions
[0787] Following injection, the Investigator will evaluate (i.e.
grade) the ease of injection including whether or not there were
technical problems such as a failure of the injection device to
inject the implant. All malfunctions of the OTX-TKI (axitinib
implant) for intravitreal use will be documented on the appropriate
CRF and reported to Ocular Therapeutix within 24 hours. Ocular
Therapeutix will advise whether the injection device will be
returned for analysis. The incidence of malfunctions will be
included in the final analysis.
Study Observations and Procedures--Cohort Group Assignment
[0788] This is an open-label, dose escalation Phase 1 study. The
Principal Investigator will make the determination of eligibility
for each subject based on the Inclusion and Exclusion criteria.
[0789] For Cohort 1, the first subject will receive the OTX-TKI
implant in the study eye before any additional subjects are
treated. Once the first subject in Cohort 1 has been evaluated for
two weeks, and the MM supports continuation, an additional five
subjects will be treated in Cohort 1.
[0790] Once Cohort 1 has been fully enrolled and all safety and
tolerability data of OTX-TKI for each subject (minimum follow up
data for two weeks) has been collected, the DSMC and MM will
conduct a review of all available clinical data.
[0791] Subjects in Cohort 2 will be treated only after: [0792] 1.
All subjects in Cohort 1 have received the OTX-TKI implant and have
been followed for at least 2 weeks [0793] 2. Confirmation that no
more than 1 out of the 6 subjects has experienced a DLT [0794] 3.
The DSMC completes a safety review of all available clinical data
and recommends dose escalation.
[0795] Once Cohorts 1 and 2 have been fully enrolled and all safety
and tolerability data of OTX-TKI for each subject (minimum follow
up data for two weeks) has been collected, the DSMC and MM will
conduct a safety review of all clinical data and will provide their
recommendations for dose escalation and continuation.
[0796] Cohort 3 will consist of approximately 12 subjects. Six
subjects will receive 600 .mu.g OTX-TKI (Cohort 3a: Monotherapy
Treatment Group), and 6 will receive 400 .mu.g OTX-TKI along with a
single anti-VEGF injection (Cohort 3b: Combination Treatment
Group). Cohort 3a (Monotherapy Treatment Group: 600 .mu.g OTX-TKI)
will be enrolled prior to Cohort 3b Combination Treatment Group
(400 .mu.g OTX-TKI along with a single anti-VEGF injection).
Study Observations and Procedures--Masking
[0797] This is an open-label unmasked safety study.
Study Observations and Procedures--Rescue Therapy
[0798] If needed, any subject in any treatment arm may receive
rescue therapy (i.e., anti-VEGF) at the Investigator's discretion.
Eligibility to receive rescue therapy will be at the Investigator's
discretion and should be communicated to the medical monitor within
3 days of treatment if not sooner. Subjects receiving rescue
therapy should return for an unscheduled visit plus SD-OCT imaging
7-10 days following treatment if no per-protocol study visit is
scheduled during that timeframe. Subjects receiving rescue therapy
will be followed to the last study visit. The following criteria
will be used to identify subjects who will likely require rescue
therapy: [0799] i. loss of 15 letters from best previous BCVA due
to ARMD, with current BCVA not better than baseline; or [0800] ii.
Loss of 10 letters on 2 consecutive visits from best previous BCVA
due to AMD, with current BCVA score not better than baseline.
[0801] iii. Evidence of worsening disease activity manifest by
greater than 75 microns CSFT from previous best value
Study Observations and Procedures--Prohibited Medications
[0802] The concomitant use of prohibited drugs with OTX-TKI must be
avoided beginning 14 days prior to the injection of the implant and
continuing for 9 months after the injection.
[0803] Co-administration of OTX-TKI and strong CYP3A4/5 inhibitors
must be avoided as the plasma bioavailability of axitinib following
intravitreal administration is not known. It has been shown that
axitinib exposure (i.e., C.sub.max) increased following
co-administration with oral ketoconazole. The following are not
permitted at any time beginning with the first screening visit:
Ketoconazole, itraconazole, clarithromycin, atazanavir, indinavir,
nefazodone, nelfinavir, ritonavir, saquinavir, telithromycin,
voriconazole.
[0804] Co-administration of OTX-TKI and strong CYP3A4/5 inducers
must be avoided as it has been shown that axitinib exposure (i.e.,
C.sub.max) decreased following co-administration with rifamycin.
The following are not permitted: Rifamycin, rifabutin, rifapentine,
phenytoin, carbamazepine, phenobaribital, hypercium (St. John's
wort). Intermittent use of topical and oral steroids is
permitted.
Study Observations and Procedures--Fundus Imaging, Fluorescein
Angiography, Optical Coherence Topography
[0805] Photographers must be certified by the Central Reading
Center before imaging of any study subjects. Imaging will follow a
standard protocol.
[0806] OCT technicians must also be certified by the Central
Reading Center. Spectral domain (SD) OCT images will be made using
the Cirrus OCT following a standard protocol.
[0807] Instructions for these procedures will be provided in a
separate imaging manual.
Study Observations and Procedures--Assessment of Pharmacokinetic
Analysis
[0808] Plasma levels of axitinib will also be determined; samples
will be taken at Screening, Baseline, Day 3 (Visit 3) and Month 3
(Visit 8). For subjects in Cohort 3 who receive three separate
OTX-TKI injections (600 .mu.g group) that may be spaced out over
1-4 weeks at Investigator's discretion, the Day 3 (Visit 3) sample
for pharmacokinetic analysis may be obtained at the same study
visit during which the third and final implant is injected.
Instructions are provided in the Lab Manual.
Study Observations and Procedures--Medical History and Concurrent
Medications
[0809] The entirety of the subject's medication treatment history
for AMD is to be recorded on the subject's source document form and
corresponding CRFs. Additionally, any other concurrent ophthalmic
medications and systemic medications, from up to 3 years prior to
the Screening Visit, are to be recorded on the subject's source
document forms and corresponding CRFs along with the reason the
medication was taken, starting at the Screening Visit through the
end of the study.
[0810] All ophthalmic and cardiac medical history for the subject
should also be recorded on the subject's source document form and
corresponding CRFs. Additional significant medical history from up
to 5 years prior to the Screening visit should be recorded on the
subject's source document form and corresponding CRFs.
Study Assessments
Screening Evaluations: Days -14 to Day 0
[0811] At the screening visit, the Principal Investigator will make
the initial determination of the subject's eligibility for study
participation by checking all inclusion and exclusion criteria. If
a subject does not meet all of the inclusion criteria and/or meets
any of the exclusion criteria the subject will be a screen failure
and no further assessments will be done. Details of the procedures
for these assessments can be found in Appendices B-G to this
section.
[0812] The following procedures and assessments may be initiated
within 14 days prior to the planned day of injection and must be
completed prior to Injection Day (Visit 2/Day 1) in the following
recommended order: [0813] Obtain written informed consent [0814]
Demographic information to include age, gender, race, ethnicity
[0815] Medical and ophthalmic history including treatment and
procedures [0816] Inclusion and exclusion criteria [0817] Prior and
concomitant medications [0818] Vital signs (pulse rate, blood
pressure, and temperature) [0819] Electrocardiogram--evidence of an
electrocardiogram within 12 weeks prior to injection Day 1 that
shows no clinically significant abnormalities (see Appendix G) must
be recorded in the CRF [0820] BCVA (ETDRS) [0821] Slit lamp
biomicroscopy and external eye exam [0822] IOP measurement by
applanation (Goldmann) tonometry [0823] Dilated fundus exam
including fundus imaging [0824] SD-OCT [0825] OCT-A [0826]
Fluorescein angiography [0827] Plasma sample for PK analysis [0828]
Safety Laboratory testing [0829] Adverse event assessment [0830]
Urine pregnancy test: if female of childbearing potential, subject
must utilize two forms of adequate contraception from screening
through the end of the study following injection of the implant,
and have a negative urine pregnancy test
[0831] NOTE: All examinations need to be performed on both
eyes.
[0832] For screen failures due to reasons that are expected to be
temporary one re-screening visit can be conducted. The re-screening
visit should be scheduled at least 14 days after the 1.sup.st
screening visit. Subjects who are re-screened will be given a new
subject number and need to have all screening procedures repeated
(including signing of a new Informed Consent). It should be noted
on the CRF that this subject is a re-screen.
[0833] For eligible subjects, all information must be recorded in
the subject's CRF. For subjects who do not meet the eligibility
criteria, the minimum information to be recorded in the CRF will be
the following: date of screening, subject number and reason for
screen failure.
Injection Day, Visit 2 (Day 1)
[0834] Prior to Injection
[0835] Prior to injection of the OTX-TKI implant the Principal
Investigator and study staff must confirm eligibility of the
subject and the study eye.
[0836] The following procedures and assessments will be performed
prior to injection of the OTX-TKI: [0837] Inclusion and exclusion
criteria confirmation [0838] Adverse events (prior to injection)
[0839] Concomitant medications [0840] Vital signs (pulse rate,
blood pressure, and temperature) [0841] BCVA (ETDRS) [0842] Slit
lamp biomicroscopy and external eye exam [0843] IOP measurement by
applanation (Goldmann) tonometry [0844] Dilated Fundus Exam [0845]
SD-OCT [0846] Ocular comfort score (to be assessed by subjects)
(pre-injection)
[0847] NOTE: All examinations need to be performed on both
eyes.
Injection Procedure
[0848] At the conclusion of all the assessments on Visit 2, Day 1
as noted above, the Investigator will confirm that the subject
continues to be eligible for the study and did not experience any
protocol defined exclusion criteria.
[0849] Subjects can have only one eye treated with OTX-TKI. If both
eyes are eligible the eye with the worse BCVA will be selected as
the study eye. If both eyes are eligible and both eyes have the
same BCVA then the Investigator will determine which eye will be
selected as the study eye.
[0850] The contralateral eye, designated as the non-study eye
(NSE), if needed, will be treated at the Investigator's discretion
with a local therapy, e.g., either topically or intravitreally
administered therapy, not systemic. This should be standard of care
and in no case should another investigational drug be used for the
contralateral eye. The contralateral eye must not be treated with
OTX-TKI. The treatment of the NSE should remain consistent for the
duration of the study.
[0851] OTX-TKI is for intravitreal use ONLY and should be
administered only by a qualified ophthalmologist experienced in the
injection procedure.
[0852] The study drug treatment will be administered by the
Investigator according to the procedure described and detailed in
the Study Reference Manual. For Cohort 3 subjects receiving 3
separate injections, at the discretion of the Investigator,
administration of the OTX-TKI implants and anti-VEGF may be spaced
out over 1-4 weeks.
Post-Injection Procedure
[0853] Subjects should be monitored for visual acuity after the
injection of OTX-TKI. Within 30-60 minutes following injection of
OTX-TKI: [0854] A Plasma sample for PK analysis will be drawn
[0855] The subject should be monitored for elevated IOP. [0856] The
subject should be monitored until the IOP is stable and <25
mmHg. The Investigator should be prepared to provide therapy in the
event of persistent elevated IOP. [0857] The Investigator should
visualize the optic nerve head at this time to verify perfusion
during the immediate post-injection period.
[0858] Prior to discharge from the visit the Investigator and study
staff are responsible to ensure that: [0859] Vision has stabilized
and that the IOP is stable and <25 mmHg [0860] Adverse events
post-injection have been recorded in the CRF [0861] The
Investigator has recorded the ease of injection procedure (i.e.,
`utilization`); the Investigator will grade the level of ease of
injection of the intravitreal implant as "easy" (1), "moderate" (2)
or "difficult" (3) [0862] Subjects are instructed to refrain from
rubbing their eyes and to contact the Investigator in the event
that they experience excessive pain, eye redness, photophobia,
excessive discomfort, or loss of vision that lasts more than a few
hours. [0863] Subjects are instructed that a member of the study
staff will reach them by telephone on the next day following the
injection of OTX-TKI to assess whether they have experienced an
Adverse Event. The subject should also be informed that they may be
asked to return to the clinic sooner that the Day 3 (Visit 3).
Post-Administration Follow up Safety Call (Day 2)
[0864] A qualified member of the study staff will telephone each
subject on the day following the injection procedure to assess
whether the subject has experienced an Adverse Event. If there is
suspicion of an Adverse Event, the subject may be asked to return
to the clinic sooner than the Day 3 (Visit 3) study visit.
Follow-Up Visit 3 (Day 3+1 Day)
[0865] Visit 3 will take place on Day 3 (+1 Day) after the
injection of OTX-TKI. At this visit the Investigator and study
staff will perform the following procedures and assessments: [0866]
Adverse events [0867] Concomitant medications [0868] Ocular comfort
score (to be assessed by subjects) [0869] BCVA (ETDRS) [0870] Slit
lamp biomicroscopy and external eye exam [0871] IOP measurement by
applanation (Goldmann) tonometry [0872] Dilated Fundus Exam
(including documentation of presence or absence of the OTX-TKI
implant) [0873] SD-OCT [0874] Plasma sample for PK analysis
[0875] NOTE: For subjects in Cohort 3 who receive three separate
OTX-TKI injections (600 .mu.g group) that may be spaced out over
1-4 weeks at Investigator's discretion, the Day 3 (Visit 3) sample
for pharmacokinetic analysis may be obtained at the same study
visit during which the third and final implant is injected (within
30-60 minutes following injection of the third and final OTX-TKI
implant a plasma sample for PK analysis will be drawn).
[0876] NOTE: All examinations need to be performed on both
eyes.
Follow-Up Visit 4 (Day 7.+-.2 Days)
[0877] Visit 4 will take place on Day 7 (+2 days) after the
injection of OTX-TKI. At this visit the Investigator and study
staff will perform the following procedures and assessments: [0878]
Adverse events [0879] Concomitant medications [0880] Ocular comfort
score (to be assessed by subjects) [0881] BCVA (ETDRS) [0882] Slit
lamp biomicroscopy and external eye exam [0883] IOP measurement by
applanation (Goldmann) tonometry [0884] Dilated Fundus Exam
(including documentation of presence or absence of the OTX-TKI
implant) [0885] SD-OCT
[0886] NOTE: All examinations need to be performed on both
eyes.
Follow-Up Visit 5 (Day 14.+-.2 Days)
[0887] Visit 5 will take place on Day 14.+-.2 days following the
injection of OTX-TKI. At this visit the Investigator and study
staff will perform the following procedures and assessments: [0888]
Adverse events [0889] Concomitant medications [0890] Vital signs
(blood pressure only) [0891] Ocular comfort score (to be assessed
by subjects) [0892] BCVA (ETDRS) [0893] Slit lamp biomicroscopy and
external eye exam [0894] IOP measurement by applanation (Goldmann)
tonometry [0895] Dilated Fundus Exam (including documentation of
presence or absence of the OTX-TKI implant) [0896] SD-OCT
[0897] NOTE: All examinations need to be perormed on both eyes.
Follow-up Assessments: Visit 6 (Month 1.+-.2 days), Visit 7 (Month
2.+-.3 days), Visit 9 (Month 4.5.+-.3 days) and Visit 11 (Month
7.5.+-.3 days)
[0898] At these visits the Investigator and study staff will
perform the following procedures and assessments: [0899] Adverse
events [0900] Concomitant medications [0901] Ocular comfort score
(to be assessed by subjects) [0902] BCVA(ETDRS) [0903] Slit lamp
biomicroscopy and external eye exam [0904] IOP measurement by
applanation (Goldmann) tonometry [0905] Dilated Fundus Exam
(including documentation of presence or absence of the OTX-TKI
implant) [0906] SD-OCT
[0907] NOTE: All examinations need to be performed on both eyes.
Pregnancy test should be performed on all females of childbearing
potential if they have missed two consecutive menstrual
periods.
Follow-up Visit 8 (Month 3.+-.3 Days) and Visit 10 (Month 6.+-.3
Days)
[0908] Visit 8 will take place 3 months+3 days and Visit 10 will
take place 6 months+3 days following the injection of OTX-TKI. At
this visit the Investigator and study staff will perform the
following procedures and assessments: [0909] Adverse events [0910]
Concomitant medications [0911] Ocular comfort score (to be assessed
by subjects) [0912] Vital signs (blood pressure only) [0913] BCVA
(ETDRS) [0914] Slit lamp biomicroscopy and external eye exam [0915]
IOP measurement by applanation (Goldmann) tonometry [0916] Dilated
fundus exam including fundus imaging and documentation of presence
or absence of the OTX-TKI implant [0917] SD-OCT [0918] OCT-A [0919]
Plasma sample for PK analysis (At Visit 8 only) [0920] Safety
Laboratory testing [0921] Additionally, at Visit 10 (Month 6) only:
[0922] Fluorescein angiography [0923] Urine pregnancy test: if
female of childbearing potential, subject must utilize two forms of
adequate contraception from screening through the end of the study
following injection of the implant, and have a negative urine
pregnancy test
[0924] NOTE: All examinations need to be performed on both eyes. At
Visit 8 (Month 3) a pregnancy test should be performed on all
females of childbearing potential if they have missed two
consecutive menstrual periods.
Final Follow-Up Visit 12 (Month 9.+-.3 Days)
[0925] This is the final follow-up visit, excluding any unscheduled
visits that may be required to follow an AE that has not resolved
or stabilized. This visit will take place 9 months (+3 days) after
injection of OTX-TKI. At this visit the Investigator should confirm
that the OTX-TKI implant is no longer visible on examination. If
the implant is still visible, the subject should be followed
approximately monthly until the implant is no longer visible. At
the Investigator's discretion, subjects who still have evidence of
biological activity at month 9 should be followed monthly until the
CNV leakage has returned to baseline levels or until the
Investigator believes the subject is clinically stable.
[0926] All of the following procedures and assessments will be
performed: [0927] Adverse event assessment [0928] Concomitant
medications [0929] Ocular comfort score (to be assessed by
subjects) [0930] Vital signs (blood pressure only) [0931]
Electrocardiogram (Appendix G) [0932] BCVA (ETDRS) [0933] Slit lamp
biomicroscopy and external eye exam [0934] IOP measurement by
applanation (Goldmann) tonometry [0935] Dilated fundus exam
including fundus imaging and documentation of presence or absence
of the OTX-TKI implant [0936] SD-OCT [0937] OCT-A [0938]
Fluorescein angiography [0939] Safety Laboratory testing [0940]
Urine pregnancy test: if female of childbearing potential, subject
must utilize two forms of adequate contraception from screening
through the end of the study following injection of the implant,
and have a negative urine pregnancy test
[0941] NOTE: All examinations need to be performed on both
eyes.
Unscheduled Visit
[0942] An unscheduled visit may occur at any time that the
Investigator decides it is necessary to see the subject outside of
the study visit windows. At the discretion of the Investigator, for
Cohort 3 subjects receiving 3 separate injections, unscheduled
visits may be used to space out administration of the OTX-TKI
implants and anti-VEGF over 1-4 weeks. As many of these visits as
necessary may be scheduled. Any unscheduled visits will be recorded
on the "unscheduled" visit CRF with the reason for the visit.
[0943] The examinations and assessments are at the Investigator's
discretion based on the reason for the visit. All examinations and
assessments, including those listed below, may be performed at
Unscheduled Visits: [0944] Adverse event assessment [0945]
Concomitant medications [0946] Ocular comfort score (to be assessed
by subjects) [0947] BCVA (ETDRS) [0948] Slit lamp biomicroscopy and
external eye exam [0949] IOP measurement by applanation (Goldmann)
tonometry [0950] Dilated Fundus Exam (including documentation of
presence or absence of the OTX-TKI implant)
Adverse Events
[0951] Throughout the course of the study, all efforts will be made
to remain alert to possible AEs or untoward findings. If an AE
occurs, the first concern will be the safety and welfare of the
subject. Appropriate medical intervention should be undertaken. Any
AEs observed by the Investigator or study staff or reported by the
subject, whether or not ascribed to the study treatment, will be
recorded on the subject's Adverse Event CRF.
[0952] Documentation regarding the AE should be made as to the
nature, date of onset, end date, severity, relationship to the
study drug, action(s) taken, seriousness, and outcome of any sign
or symptom observed by the physician or reported by the
subject.
Definition of an Adverse Event
[0953] An AE is any untoward medical occurrence in a patient or
clinical investigation subject administered a pharmaceutical
product and which does not necessarily have a causal relationship
with the treatment.
[0954] An AE can therefore be any unfavorable and unintended sign
(including an abnormal laboratory finding), symptom or disease
temporally associated with the use of a medicinal (investigational)
product, whether or not related to the medicinal (investigational)
product.
Definition of a Serious Adverse Event (SAE)
[0955] An SAE is any untoward medical occurrence that at any dose:
[0956] Results in death [0957] Is life-threatening [0958] The term
"life-threatening" refers to an event in which the subject was at
risk of death at the time of the event; it does not refer to an
event which hypothetically might have caused death if it were more
severe [0959] Requires in-patient hospitalization or prolongation
of existing hospitalization [0960] Results in persistent or
significant disability/incapacity [0961] Is a congenital
abnormality/birth defect
[0962] Medical and scientific judgment should be exercised in
deciding whether other situations should be considered SAEs, such
as important medical events that might not be immediately
life-threatening or result in death or hospitalization but might
jeopardize the subject or might require intervention to prevent one
of the other outcomes listed above.
[0963] Examples of such events are intensive treatment in an
emergency room or at home for allergic bronchospasm, blood
dyscrasias, neoplasms or convulsion that do not result in
hospitalization.
[0964] An AE that is assessed as `severe` should not be confused
with an SAE. The term "severe" is often used to describe the
intensity (i.e., severity) of a specific event (as in mild,
moderate, or severe myocardial infarction); the event itself,
however, may be of relatively minor medical significance (such as a
severe headache). This is not the same as "serious", which is based
on the outcome or action criteria usually associated with events
that pose a threat to life or functioning. Seriousness (not
severity) and causality serve as a guide for defining regulatory
reporting obligations.
Severity
[0965] Severity of an AE is defined as a qualitative assessment of
the degree of intensity of the AE as determined by the Investigator
or reported to the Investigator by the subject. The assessment of
severity is made irrespective of relationship to the study drug or
seriousness of the event and should be evaluated according to the
following scale: [0966] Mild Event is noticeable to the subject,
but is easily tolerated and does not interfere with the subject's
daily activities [0967] Moderate Event is bothersome, possibly
requiring additional therapy, and may interfere with the subject's
daily activities [0968] Severe Event is intolerable, necessitates
additional therapy or alteration of therapy, and interferes with
the subject's daily activities
[0969] For AEs that change in intensity, the start and stop date of
each intensity should be recorded.
Relationship to Intravitreal Implant, Procedure, or Study Drug
[0970] For each (S)AE, the Investigator must determine whether the
event is related to the study drug, the injection procedure or the
intravitreal implant. In order to do so, the Investigator must
determine whether, in his/her medical judgment, there is a
reasonable possibility that the event may have been caused by the
study drug, the injection procedure or the intravitreal
implant.
[0971] The following is a guideline to be used by the Investigator
as a guide when assessing the causal relationship of an (S)AE. The
attribution of causality to the injection procedure, the
intravitreal implant or the study drug will be identified in the
CRF. [0972] No RELATIONSHIP SUSPECTED This category applies to
those (S)AEs which, after careful consideration, are clearly and
incontrovertibly due to extraneous causes (disease, environment,
etc.); there is no reasonable probability that the (S)AE may have
been caused by the study drug, the injection procedure, or the
intravitreal implant [0973] RELATIONSHIP SUSPECTED The following
criteria should be applied in considering inclusion of an (S)AE in
this category: [0974] 1) It bears a reasonable temporal
relationship to the injection procedure or the presence of the
intravitreal implant or the study drug [0975] 2) It could not be
reasonably explained by the known characteristics of the subject's
clinical state, environmental or toxic factors or other factors
(e.g., disease under study, concurrent disease(s) and concomitant
medications) and modes of therapy administered to the subject
[0976] 3) It disappears or decreases on removal of the intravitreal
implant [0977] 4) It follows a known pattern of response to the
injection procedure or the intravitreal implant or the study
drug
[0978] Where the causal relationship of the AE to the injection
procedure or the intravitreal implant has not been determined, or
is unknown, the AE will be treated as if a relationship is
suspected for the purposes of regulatory reporting.
[0979] A suspected AE is any event for which there is a reasonable
possibility that the study drug caused the AE. "Reasonable
possibility" means there is evidence to suggest a causal
relationship between the study drug and the AE. Types of evidence
that would suggest a causal relationship between the study drug and
the AE include: a single occurrence of an event that is uncommon
and known to be strongly associated with drug exposure; one or more
occurrences of an event that is not commonly associated with drug
exposure, but is otherwise uncommon in the population exposed to
the drug (e.g., tendon rupture); an aggregate analysis of specific
events observed in a clinical trial (such as known consequences of
the underlying disease or condition under investigation or other
events that commonly occur in the study population independent of
drug therapy) that indicates those events occur more frequently in
the drug treatment group than in a concurrent or historical control
group.
Expectedness
[0980] The expectedness of an (S)AE should be determined based upon
existing safety information about the study drug using these
guidelines: [0981] UNEXPECTED: An AE or that is not listed in the
study protocol, IB, or prescribing information for the registered
formulation of axitinib (INLYTA.RTM.) or is not listed at the
specificity or severity that has been observed [0982] EXPECTED: An
AE that is listed in the study protocol, IB, or prescribing
information for axitinib at the specificity and severity that has
been observed
[0983] AEs that are mentioned in the IB as occurring with a class
of drugs or as anticipated from the pharmacological properties of
the drug but are not specifically mentioned as occurring with the
particular drug under investigation are to be considered as
expected.
[0984] The Investigator should initially classify the expectedness
of an AE, but the final classification is subject to the Medical
Monitor's determination.
Clarifications
[0985] Hospitalization
[0986] Hospitalization for the elective treatment of a pre-existing
condition (i.e., a condition present prior to the subject's
signature of the Informed Consent) that did not worsen during the
study is not considered an SAE. Complications that occur during
hospitalization are AEs. If a complication prolongs
hospitalization, or meets any of the other SAE criteria, the
complication is an SAE.
[0987] Pre-Existing Conditions
[0988] Pre-existing conditions (i.e., conditions present or
detected at the start of the study) which worsen during the study,
exacerbation of a pre-existing illness or an increase in frequency
or intensity of a pre-existing episodic event or condition are
(S)AEs. Anticipated day-to-day fluctuations of pre-existing
condition(s) that do not worsen with respect to baseline are not
(S)AEs.
[0989] Worsening or progression of wet AMD is considered to be a
"lack of efficacy" or "failure of expected pharmacological action"
per protocol and is already recorded as part of the efficacy
assessment and therefore does not need to be recorded as an (S)AE.
However, the signs and symptoms and/or clinical sequelae resulting
from the lack of efficacy may be reported as an (S)AE if considered
by the Investigator to fulfill the definition of an (S)AE.
[0990] Medical or Surgical Procedures
[0991] Medical or surgical procedures (e.g., colonoscopy) are not
(S)AEs; however, the condition that leads to the procedure may be
considered an (S)AE.
[0992] In the case of elective medical or surgical procedures, or
pre-study planned medical or surgical procedures for pre-existing
conditions (i.e., a condition present prior to the subject's
signature of the Informed Consent) that did not worsen during the
study the condition that leads to the procedure does not need to be
reported as an (S)AE.
[0993] Death
[0994] Death is not an SAE; the condition that leads to the death
is an SAE.
[0995] Abnormal Laboratory Values
[0996] In the absence of a diagnosis, abnormal laboratory values
that are judged by the Investigator to be clinically significant
must be recorded as an (S)AE. Clinical significant abnormal
laboratory findings that are present at baseline and significantly
worsen following the start of the study will also be reported as an
(S)AE.
Procedures for Reporting Adverse Events
[0997] All AEs that are "Suspected" and "Unexpected" are to be
reported to Ocular Therapeutix and the IRB as required by the
IRB/IEC, local regulations and the governing Health
Authorities.
[0998] All AEs observed during the course of this study from the
time the subject signs the Informed Consent, regardless of severity
or relationship to the study drug or intravitreal implant will be
recorded on the appropriate CRF(s). To the extent possible, the
event to be recorded and reported is the event diagnosis as opposed
to the event symptoms.
[0999] Any Serious Adverse Event or any severe, sight-threatening
AE, whether ascribed to the study treatment or not, will be
communicated within 24 hours, by telephone, to Ocular Therapeutix
or its designee. The Investigator must obtain and maintain in
his/her files all pertinent medical records, information, and
medical judgments from colleagues who assisted in the treatment and
follow-up of the subject; provide Ocular Therapeutix or its
designee with a complete case history, which includes a statement
as to whether the event was or was not suspected to be related to
the use of the study drug; and inform the IRB/IEC of the AE within
the IRB/IEC guidelines for reporting SAEs. A written report
detailing the event, signed by the Investigator, shall be submitted
to the Sponsor or its designee within 5 working days. All subjects
who experience an SAE must be followed until resolution or
stabilization of the event and the outcome is reported in the
CRF.
Type and Duration of the Follow-Up of Adverse Events
[1000] AEs will be followed until: [1001] Resolution of the event,
i.e., return to the baseline value or status or to `normal` [1002]
AEs may be determined to have resolved completely or resolved with
sequelae [1003] The Investigator determines, for events that do not
end (e.g. metastasis), the condition to be chronic; the event can
be determined to be resolved or resolved with sequelae [1004] The
event has stabilized, i.e., no worsening expected by the
Investigator. All AEs will be documented in the CRFs.
[1005] For subjects that reach the final scheduled visit (i.e.
Visit 12 [Month 9]), an unscheduled visit may be conducted
thereafter to follow-up on any AEs that the Investigator has not
deemed to be resolved or stabilized.
Dose Escalation Criteria and Stopping Criteria
[1006] Due to limited human experience with the OTX-TKI implant,
the first subject in Cohort 1 will receive the OTX-TKI implant in
the study eye before any additional subjects are treated
[1007] Once the first subject Cohort 1 has been evaluated for 2
weeks, and if the MM supports continuation, an additional 5
subjects will be treated in Cohort 1.
[1008] Subjects will be treated in Cohort 2 only after: [1009] 1.
All subjects in Cohort 1 have received the OTX-TKI implant and have
been followed for at least 2 weeks [1010] 2. Confirmation that no
more than 1 out of the 6 subjects has experienced a DLT [1011] 3.
The DSMC completes a safety review of all available clinical data
and recommends dose escalation.
[1012] If one DLT is identified in Cohorts 1, 2, or 3a, enrollment
will continue until the cohort has been fully enrolled. If a second
DLT is seen in Cohorts 1 or 2, then enrollment will stop. If a
second DLT is seen in Cohort 3a, enrollment in that cohort will
stop and the previous lower dose will be declared the MTD.
[1013] All subjects dosed prior to the decision to stop study
enrollment are to continue to be followed per the protocol. The
decision to stop further enrollment in a particular cohort will be
made by the MM based on recommendations from the DSMC.
[1014] The specific DLT's which may warrant stopping further
enrollment include (but are not limited to): [1015] Ocular
inflammation of 4+ or ocular inflammation of 2-3+ that does not
decrease to .ltoreq.1+ within 30 days of onset [1016] BCVA decrease
of >15 letters on multiple consecutive visits compared to
pre-treatment due to study drug [1017] Increase in IOP of >10
mmHg or an IOP of >30 mmHg that does not return to pre-injection
levels within 7 days of treatment
Statistical Methods
Statistical and Analytical Plans
[1018] This study is not designed to show statistical significance,
therefore, there will be no statistical analyses completed. There
will be a general Statistical Plan that will briefly summarize how
the data will be presented, i.e., descriptive statistics, etc.
Determination of Sample Size
[1019] For this Phase I study, no formal sample size calculations
have been performed. The study will enroll up to 6 subjects in the
first cohort and the accumulated data will be reviewed by the DSMC
before continuing enrollment in the second cohort. After the second
cohort of up to 8 subjects has been enrolled, the DSMC and MM will
review the accumulated data and provide a recommendation for dose
escalation and continuation to Cohort 3, which will enroll up to 12
subjects.
Analysis Datasets
[1020] The safety population will consist of all subjects receiving
the OTX-TKI implant. All safety and efficacy analyses will be
performed on the safety population.
Demographics and Baseline Data
[1021] Subject disposition will be presented, including the number
of subjects screened, enrolled and treated. The number of subjects
who completed the study and reasons for discontinuation will be
summarized. Data will be presented by cohort group and overall.
[1022] Demographic and baseline characteristics (including disease
and medical history) will be summarized. Data will be presented by
cohort group and overall.
Safety Analyses
[1023] Safety will be assessed by ocular and systemic adverse
events, ocular comfort score assessment and other ocular-related
outcomes.
[1024] Adverse events will be coded using Medical Dictionary for
Regulatory Activities (MedDRA) by system organ class and preferred
term. Separate summaries will be made for adverse events that are
related to the study drug, the injection procedure and the OTX-TKI
implant. In addition, serious adverse events will be
summarized.
Summaries .times. .times. of .times. .times. other .times. .times.
safety .times. .times. .times. related .times. .times. outcomes
.times. .times. will .times. .times. be .times. .times. provided .
.times. All .times. .times. safety .times. .times. data .times.
.times. will .times. .times. be .times. .times. presented .times.
.times. by .times. .times. hort .times. .times. group .times.
.times. and .times. .times. overall . ##EQU00001##
Efficacy Analyses
[1025] Efficacy will be assessed by mean change in CSFT from
baseline, mean change in BCVA from baseline, percent of subjects
with clinically significant change in leakage, percent of subjects
with a decrease in CSFT of 50 .mu.m, percentage of subjects with
SRF, IRF and both SRF and IRF and percent of subjects who needed
rescue therapy. Data will be presented by treatment group and
overall.
Pharmacokinetic Data
[1026] Systemic OTX-TKI exposure as measured in blood samples will
be summarized at each time point. Plasma concentrations and
pharmacokinetic parameters will be summarized by treatment group
and overall. Measured concentrations and pharmacokinetic parameters
will be presented in data listings.
ABBREVIATIONS
TABLE-US-00025 [1027] List of abbreviations used for describing the
study details: Abbreviation Meaning AE Adverse Event AMD/ARMD
Age-related Macular Degeneration API Active Pharmaceutical
Ingredient BCVA Best Correct Visual Acuity BRB Blood Retinal
Barrier CNV Choroidal Neovascularization CNVM Central Neovascular
Membrane COVID-19 Coronavirus Disease 2019 CRC Central Reading
Center CRF Case Report Form CSFT Central Subfield Thickness DLT
Dose Limiting Toxicity DME Diabetic Macular Edema DR Diabetic
Retinopathy DSMC Data Safety Monitoring Committee ECG
Electrocardiography ERG Electroretinography ETDRS Early Treatment
Diabetic Retinopathy Study FA Fluorescein Angiography FDA Food and
Drug Administration GCP Good Clinical Practice IB Investigator's
Brochure ICH International Conference on Harmonization IEC
Independent Ethics Committee IOP Intraocular Pressure IRB
Institutional Review Board IRF Intraretinal Fluid IVT Intravitreal
(Intravitreous) MM Medical Monitor MTD Maximum Tolerated Dose NSE
Non-study eye NVAMD Neovascular Age-Related Macular Degeneration
OCT - (A) Ocular Coherence Tomography (angiography) OHT Ocular
Hypertension OTX-TKI Ocular Therapeutix Axitinib Implant for
Intravitreal Use PEG Polyethylene glycol PLA Polylactide PVD
Posterior Vitreous Detachment RCC Renal Cell Carcinoma RPE Retinal
Pigment Epithelium SAE Serious Adverse Event SD-OCT Spectral Domain
Optical Coherence Tomography SE Study eye SFNV Subfoveal
Neovascularization SRF Subretinal Fluid TGA Therapeutic Goods
Association TKI Tyrosine Kinase Inhibitor VEGF Vascular Endothelial
Growth Factor
APPENDICES TO THE STUDY PROTOCOL
TABLE-US-00026 [1028] APPENDIX A TIME AND EVENT SCHEDULE Visit Type
Screening/ Follow- Follow- Follow- Follow- Baseline Follow-up
Follow- Follow-up up up up up Visit Injection Telephone up Day Day
Month Month Month Day -14 to Day.sup.b Call Day 3 +1 7 .+-. 2 14
.+-. 2 1 .+-. 2 2 .+-. 3 3 .+-. 3 Day 0 Day 1 Day 2 day days days
days days days Visit Number Visit 1 Visit 2 N/A Visit 3 Visit 4
Visit 5 Visit 6 Visit 7 Visit 8 Informed Consent X Demographic X
Information Medical and X Ophthalmic History including treatment
and procedures Inclusion and X X Exclusion Criteria Prior and X X X
X X X X X Concomitant Medication Adverse events X X X X X X X X
Ocular Comfort .sup. X.sup.e X X X X X X Score (to be assessed by
subiects) Vital signs.sup.c X X X X ECG X BCVA (ETDRS) X X X X X X
X X Slit lamp X X X X X X X X biomicroscopy and external eye exam
IOP Measurement X X X X X X X X by Goldmann Dilated Fundus X X X X
X X X X Exam (including presence or absence of OTX- TKI) Fundus
Imaging X X SD-OCT X X X X X X X X OCT-A X X Fluorescein X
angiography Injection of OTX- X TKI implant Post-administration X
follow-up safety call Urine Pregnancy X test.sup.f Plasma sample
for X .sup. X.sup.g .sup. X.sup.h X PK Safety Laboratory X X
analysis.sup.d Visit Type Final Follow-up Follow-up Follow-up
Follow-up Month Month Month Month Un- 4.5 .+-. 3 6 .+-. 3 7.5 .+-.
3 9 .+-. 3 scheduled days days days days Visit.sup.a Visit Number
Visit 9 Visit 10 Visit 11 Visit 12 Informed Consent Demographic
Information Medical and Ophthalmic History including treatment and
procedures Inclusion and Exclusion Criteria Prior and Concomitant X
X X X X Medication Adverse events X X X X X Ocular Comfort Score
(to be X X X X X assessed by subjects) Vital signs.sup.c X X X ECG
X X BCVA (ETDRS) Manifest X X X X X Refraction Slit lamp
biomicroscopy and X X X X X external eye exam IOP Measurement by X
X X X X Goldmann Dilated Fundus Exam X X X X X (including presence
or absence of OTX-TKI) Fundus Imaging X X X SD-OCT X X X X X OCT-A
X X X Fluorescein angiography X X X Injection of OTX-TKI implant
Post-administration follow-up safety call Urine Pregnancy
test.sup.f X X X Plasma sample for PK Safety Laboratory
analysis.sup.d X X X .sup.aFor any Unscheduled Visit the
Investigator should determine which assessments need to be
performed based on the reason for the unscheduled visit; not all
assessments need be performed (see section 8.12 for list of
required assessments). .sup.bSubjects will be monitored 30-60
minutes post injection (see section 8.5 for details regarding
post-injection monitoring); for Cohort 3, injections of the OTX-TKI
implants and anti-VEGF may be spaced out over 1-4 weeks at the
Investigator's discretion. .sup.cVital signs will encompass
assessment of blood pressure, pulse rate and temperature at visits
1 and 2 only. At all other visits only the blood pressure
measurement will be performed. .sup.dSafety laboratory assessments
comprise: CBC, Chem-7, LFTs and TFT. .sup.eOcular Comfort Score to
be assessed by subjects' pre-injection of OTX-TKI on Visit 2 (Day
1). .sup.fPregnancy test will be performed on all females of
childbearing potential at the Screening/Baseline Visit (Days -14 to
0), Visit 10, Visit 12 and at any time that the subject has missed
2 consecutive menstrual periods. .sup.gPlasma sample for PK to be
performed 30-60 minutes post-injection of OTX-TKI on Visit 2 (Day
1). .sup.hFor subjects in Cohort 3 who receive three separate
OTX-TKI injections (600 .mu.g group) that may be spaced out over
1-4 weeks at Investigator's discretion, the Day 3 (Visit 3) sample
for pharmacokinetic analysis may be obtained at the same study
visit during which the third and final implant is injected (within
30-60 minutes following injection of the third and final OTX-TKI
implant a plasma sample for PK analysis will be drawn).
APPENDIX B: OCULAR COMFORT SCORE (TO BE ASSESSED BY SUBJECTS)
[1029] Subjects will be asked to grade their comfort level by
asking them the following question: "On a scale of 0 to 10, 0 being
very comfortable and 10 being very uncomfortable, how comfortable
does your eye feel at this time?"
[1030] The examiner will record the number selected by the subject
in whole numbers on the appropriate CRF.
APPENDIX C: RECOMMENDED PROCEDURES FOR BEST CORRECTED VISUAL ACUITY
(BCVA)
[1031] Visual Acuity should be evaluated at the beginning of each
study visit prior to performing other tests such as Goldmann
tonometry and gonioscopy and prior to pupil dilation. Every effort
should be made to have the same BCVA assessor throughout the study
period. Visual acuity testing should be done starting with most
recent correction.
[1032] BCVA should be measured using a backlit ETDRS chart such as
Precision Vision's or equivalent. It is recommended that the site
use a backlit, wall-mounted or caster stand ETDRS distance eye
chart with a luminance of 85 cd/m.sup.2 set at 4 meters from the
subject. A trial lens frame, or phoropter, set at 12.0 mm vertex
distance should be used to obtain manifest refraction measurements.
If possible, final refinement of sphere should be done at 4 meters
with a trial lens set.
[1033] Eye Charts
[1034] All distance visual acuity measurement should be made using
an Illuminator Box (or equivalent) set at 4 meters from the
subject. Any subject unable to read at least 20 or more letters on
the ETDRS chart at 4 meters should be tested at 1 meter according
to the instructions provided for 1 meter testing. The fluorescent
tubes in the light box should be checked periodically for proper
functioning.
[1035] A maximum effort should be made to identify each letter on
the chart. When the subject says he or she cannot read a letter, he
or she should be encouraged to guess. If the subject identifies a
letter as one of two letters, he or she should be asked to choose
one letter and, if necessary, to guess. When it becomes evident
that no further meaningful readings can be made, despite
encouragement to read or guess, the examiner should stop the test
for that eye. However, all letters on the last line should be
attempted as letter difficulties vary and the last may be the only
one read correctly. The number of letters missed or read
incorrectly should be noted.
[1036] LogMAR Visual Acuity Calculations
[1037] The last line in which a letter is read correctly will be
taken as the base logMAR reading. To this value will be added the
number "N.times.0.02" where `N` represents the total number of
letters missed up to and included in the last line read. This total
sum represents the logMAR visual acuity for that eye.
[1038] For Example: Subject correctly reads 4 of 5 letters on the
0.2 line, and 2 of 5 letters on the 0.1 line.
TABLE-US-00027 Base logMAR = 0.1 N (total number of letters
incorrect = 4 on line 0.2 as well as 0.1) N .times. T (T = 0.02) =
0.08 Base logMAR + (N .times. T) = 0.1 + 0.08 logMAR VA = 0.18
[1039] BCVA examination should begin with the right eye (OD). The
procedure should be repeated for the left eye (OS).
[1040] 1-Meter Testing
[1041] The subject must sit for the 1-meter test. The avoidance of
any head movement forward or backward is particularly important
during this test.
APPENDIX D: SLIT LAMP BIOMICROSCOPY EXAMINATION
[1042] The slit beam observations should be assessed in a dark room
using the highest lamp voltage, an aperture of 0.3 mm, an
illumination angle of 30 degrees and a magnification of
16.times..
[1043] The clinician will use a slit lamp to assess the following
as normal, abnormal clinically significant or abnormal not
clinically significant: [1044] External adnexa--Presence or absence
of lid erythema, edema or other abnormalities, evaluation of lashes
for scurf or other abnormalities [1045] Conjunctiva--presence or
absence of edema, erythema or other abnormalities [1046]
Iris--presence or absence of stromal or other abnormalities [1047]
Cornea--clarity, presence or absence of superficial punctate
keratopathy or other abnormalities assess with fluorescein stain
[1048] Anterior Chamber--adequacy of formation depth, cell score
and flare count [1049] Lens--presence or absence of cataract, and
severity of opacity, presence or absence of pseudophakia
[1050] Explanation/comments should be provided on the CRF for any
abnormal observations. If a corneal edema is observed, a notation
on whether it is general or local should be added.
[1051] Anterior Chamber Cells and Flare
[1052] Assessment of anterior chamber cells should be performed as
follows: [1053] Low ambient lighting [1054] 1.times.1 mm slit beam
[1055] Highest slit lamp voltage [1056] Illumination angle of 45
degrees [1057] High magnification
[1058] The anterior chamber will be examined for the presence of
signs of ocular inflammation. Anterior chamber cell count and flare
will be graded using the SUN* Working Group grading scheme:
Although an anterior chamber cell grade of "0" is reported as
"<1 cell" in the SUN Working Group grading scheme, it will be
characterized as 0 cells in the field for this study.
[1059] The anterior chamber cell count will be assessed as the
actual number of cells counted within the slit beam of 1.0 mm
height and 1.0 mm width described above, if fewer than 16 cells are
seen. Only white blood cells will be counted. (Red blood cells and
pigment cells are not to be counted). The number of cells counted
and the corresponding grade per the below scale will both be
recorded in the CRF.
TABLE-US-00028 Anterior Chamber Cells Grade Number of Cells in
Field 0 0 (rare cells, i.e.. one cell in a minority of fields) 0.5+
1-5 (trace) 1+ 6-15 (cells) 2+ 16-25 (cells) 3+ 26-50 (cells) 4+
>50 (cells) Flare Grade Description 0 None 1+ Faint 2+ Moderate
iris and tens details clear 3+ Marked iris and tens details hazy 4+
Intense fibrin or plastic aqueous *Standardization of the Uveitis
Nomenclature (SUN).sup.1 If hypopyon is present, this should be
noted in the source documents and eCRF. .sup.1Jabs D A, Nussenblatt
R B, Rosenbaum J T. Standardization of Uveitis Nomenclature (SUN)
Working Group. Standardization of uveitis nomenclature for
reporting clinical data. Results of the First International
Workshop. Am J Ophthalmol. 2005 September; 140(3): 509-16.
APPENDIX E: IOP MEASUREMENT
[1060] Goldmann tonometry as the international gold standard for
tonometry is quite accurate and reproducible if proper technique is
used. When performing Goldmann tonometry the following procedures
should be followed: [1061] 1. Pre-tonometry procedures: Set
tonometer in the correct position and make sure the prism is in the
horizontal position on the slit lamp. Set the tension at 1 mmHg.
Use Cobalt filter with slit beam open maximally with the angle
between the illumination and the microscope at approximately 60
degrees. [1062] 2. Instill one drop of a topical anesthetic and a
moistened fluorescein strip may be lightly touched against the
tarsal conjunctiva of the lower lid of each eye, taking care not to
flood the ocular surface with fluorescein dye. Alternatively, a
drop of topical anesthetic-fluorescein (e.g., Fluress) solution may
be instilled into the lower conjunctival fornix of each eye, taking
care not to flood the ocular surface with fluorescein dye. Ask
subject to blink a few times just prior to tonometry. [1063] 3.
Place subject in adjustable chair so chin can fit comfortably on
the slit lamp chin rest and the forehead can be snug against the
forehead bar. [1064] 4. Apply tonometer to the subject's eye while
subject looks straight ahead and increase the force of applanation
until the observer sees the inner portion of the two half
fluorescein circles are touching. Record pressure on the CRF.
APPENDIX F: DILATED FUNDUS EXAM
[1065] Assessments should be conducted using indirect
ophthalmoscopy. Each of the following will be evaluated and
documented as normal, abnormal clinically significant or abnormal
not clinically significant: [1066] Vitreous: When examining the
vitreous, the Investigator should also document the presence or
absence of the OTX-TKI implant at the macula, peripheral retina,
choroid, and optic nerve.
[1067] The cup to disc (C/D) ratio will also be measured.
Explanation/comment should be provided on the CRF for any abnormal
pathology.
[1068] The following scale will be used to define the extent of
vitreous hazel:
TABLE-US-00029 Absent Clear view of optic disc, retinal vessels and
nerve fiber layer Trace Slight blurring of optic disc margin and of
normal striations and reflex of nerve fiber layer cannot be
visualize 1+ Mild blurring of optic disc margin and slight loss of
retinal vessel definition 2+ Moderate blurring of optic disc margin
and loss of retinal vessel definition 3+ Optic nerve head and large
vessels visible but borders quite (very) blurry 4+ Optic nerve head
obscured .sup.2Nussenblatt R B, Palestine A G, Chan C C, Roberge F.
Standardization of vitreal inflammatory activity in intermediate
and posterior uveitis. Ophthalmology 92: 467-471, 1985.
APPENDIX G: ELECTROCARDIOGRAM (ECG)
12-lead ECG
[1069] A 12-lead ECG will be performed during the Screening Phase.
An ECG will be performed after the subject has been supine for
approximately 3 minutes. Sites are to use their own, local ECG
machines for the study and the ECG readings will be interpreted by
the Investigator (or delegated qualified designee) by clinically
correlating with the subject's condition.
[1070] The Investigator's interpretation will be recorded in the
ECG eCRF as: normal; abnormal, not clinically significant; or
abnormal, clinically significant. Results must be within normal
limits or not clinically significant in order to allow a subject to
continue in the study.
Example 6.3: Initial Results of the Study
[1071] Initial studies were performed in human subjects as follows:
Subjects with neovascular age-related macular degeneration (nAMD,
both treatment-naive and those with a history of anti-VEGF therapy)
were enrolled for administration of inventive hydrogel in a single
study eye. Two groups completed enrollment and are under
evaluation: 200 .mu.g axitinib in a 7.5% PEG hydrogel (formed from
2 parts 4a20K PEG-SAZ to 1 parts 8a20K PEG amine) where the 7.5%
represents the PEG weight divided by the fluid weight.times.100 (1
implant; n=6) and 400 .mu.g axitinib (2 implants; n=7).
Spectral-domain optical coherence tomography (SD-OCT) imaging was
used to assess retinal fluid and central subfield thickness (CSFT)
was performed at Baseline. Injection visits occurred at days 3, 7,
and 14, and at months 1, 2, 3, 4.5, 6, 7.5, 9, and approximately
monthly until implant(s) were no longer visible. The inventive
implants were visualized at every visit. Safety evaluations
included: adverse event collection, vital signs, best-corrected
visual acuity (BCVA), slit lamp biomicroscopy, tonometry, indirect
and direct ophthalmoscopy and safety labs.
[1072] In the 400 .mu.g group, an average reduction in central
subfield thickness (CSFT) of 89.8.+-.22.5 .mu.m (mean.+-.SEM) was
observed by 2 months and was generally maintained through the 3
month timepoint (follow-up ongoing). For several subjects with a
history of anti-VEGF therapy, the durability of anti-VEGF treatment
was extended to >9 months in the 200 .mu.g group and >3
months in the 400 .mu.g group (follow-up ongoing). Best-corrected
visual acuity (BCVA) was maintained with no serious ocular adverse
events reported. The most common adverse events observed in the
study eye include tiny pigmented keratic precipitates (3/13),
subretinal hemorrhage (2/13) and subconjunctival hemorrhage (3/13)
and pain (2/13) following implant injection. Implant(s) exhibited
little movement in the vitreous and were no longer visible after
9-10.5 months in the 200 .mu.g group.
[1073] The inventive implants were generally well-tolerated with a
favorable safety profile. Minimal movement and consistent
resorption of implant(s) has been observed up to 10.5 months.
[1074] Detailed results of the continuation of these initial
studies with 200 .mu.g (1 implant) and 400 .mu.g (2 implants)
axitinib doses and additional studies with a 600 .mu.g (3 implants)
axitinib dose as well as a 400 .mu.g (2 implants) axitinib dose
concurrently administered with an anti-VEGF agent are reported in
detail in Example 6.4.
Example 6.4: Comprehensive Results of the Study
Evaluation of Doses of 200 and 400 .mu.g Axitinib
[1075] As explained in the study protocol reproduced above,
participants of cohort 1 (n=6) received one implant comprising an
axitinib dose of 200 .mu.g in one eye per patient and participants
of cohort 2 (n=7) received two implants each comprising an axitinib
dose of 200 .mu.g in one eye per patient resulting in 400 .mu.g
dose in total per eye. Implants were administered intravitreally
using a 27 G needle. Even in the hydrated state the implants did
not result in visual impact due to their compact size and shape.
Patients of cohort 2 received the two implants on the same day,
with the exception of subject #2 who received the implants 1 week
apart. For formulation details and dimensions of the 200 .mu.g
implant used in this study see Table 21.1 (Implant #1). Overview
charts presenting summary data regarding central subfield thickness
(CSFT) and best corrected visual acuity (BCVA) of all subjects
enrolled and analyzed so far in cohorts 1 and 2 are provided in
FIGS. 17 and 18, respectively. In addition, in order to exemplary
illustrate the course of CSFT and BCVA in subjects of cohorts 1 and
2, certain specific subjects are discussed herein in more detail,
and images showing the CSFT and BCVA in these subjects at exemplary
visits are provided in the Figures. These exemplary subjects are
discussed to illustrate CSFT and BCVA measurement and development
in subjects/patients who participated in the study, but are
singular subjects. For the mean change of CSFT and BCVA over all
subject of cohorts 1 and 2, it is referred to FIGS. 17 and 18. For
FIGS. 17 and 18, six patients were followed in cohort 1 until month
9. Seven patients were followed in cohort 2 until month 12, five
until month 14 and two until month 16.
[1076] 31% (4 of 13) patients in cohorts 1 and 2 were female, 69%
(9 of 13) were male with a median age of 75.2 years (standard
deviation, SD: 4.5), wherein the youngest patient was 67 and the
oldest patient 83 years. Participants of both cohorts were either
previously treated with anti-VEGF therapeutic (such as ranibizumab
or aflibercept) or naive. An overview of the subjects from cohort 1
and 2 is further given in Table 22. The baseline CSFT for the 6
treated subjects in cohort 1 is 680.+-.159 .mu.m (mean.+-.SE), and
the baseline BCVA (Snellen equivalent) is 0.73.+-.0.26
(mean.+-.SE). The baseline CSFT for the 7 treated subjects in
cohort 2 is 450.+-.29 .mu.m (mean.+-.SE), and the baseline BCVA
(Snellen equivalent) is 0.47.+-.0.17 (mean.+-.SE).
TABLE-US-00030 TABLE 22 Overview of subjects from the two cohorts
(cohort 1 and 2). Age, Sex (male M, female F), together with prior
treatment and study eye are presented. For the study eye (oculus
dexter, (OD) or oculus sinister (OS)), pre- treatment BCVA is given
as logMAR (logarithm of the minimal angle resolution) and Snellen
equivalent. A conversion chart from EDTS letter score to LogMAR
value and Snellen equivalent can be found in Beck et al., Am 3
Ophthalmol 2003, 135: 194-205. In addition, CSFT pre-treatment is
presented. All pre-treatment results are from day 1 of the study,
except for cohort 1, subjects 3, 4, and 5 for which data was taken
from the screening visit. Study Eye Pre- Treatment Pre- Pre-
Subject logMAR Treatment Treatment No. Age Sex Prior Treatment
Study Eye BCVA Snellen BCVA CSFT (pm) Cohort 1 (200 .mu.g) #1 74 M
Nave OS 1.14 @ 1 m 20/276 1252 #2 71 M Anti-VEGF OD 0 20/20 350 #3
79 M Anti-VEGF OD 0.30 20/40 309 #4 73 F Anti-VEGF OS 1.52 @ 1 m
20/662 742 #5 80 M Anti-VEGF OS 0.36 20/46 408 #6 78 M Nave OD 1.04
@ 1 m 20/219 1030 Cohort 2 (400 .mu.g) #1 72 M Anti-VEGF OD -0.04
20/18 473 #2 75 F Nave OS 1.40 @ 1 m 20/502 513 #3 67 M Anti-VEGF
OS 0.36 20/46 561 #4 80 M Anti-VEGF OS 0.28 20/38 448 #5 71 M Nave
OD 0.42 20/53 430 #6 83 F Anti-VEGF OS 0.30 20/40 388 #7 75 F
Anti-VEGF OD 0.54 20/69 335
[1077] Participants were evaluated for changes in central subfield
thickness (CSFT) and retinal fluid by spectral domain optical
coherence tomography (SD-OCT), for best corrected visual acuity
(BCVA), and for clinically-significant leakage using fluorescein
angiography (FA) and/or OCT prior to treatment (baseline
values--day 1), on days 3, 7, and 14, and months 1, 2, 3, 4.5, 6,
7.5, 9, 10.5, 11, 12, 13.5, 14, and/or 15.5 and approximately
monthly for the subjects still in the study until the implants were
no longer visible. In addition, slit lamp biomicroscopy, tonometry
(for measurement of IOP), and indirect and direct ophthalmoscopy
were performed on the study visits. Patients were monitored for
adverse events on all study visits.
Biodegradation
[1078] Implants exhibited little movement in the vitreous.
Generally, implants were no longer visible after 9-12 months in
both cohorts. FIG. 15 exemplarily shows IR images for subject #1 of
cohort 2.
Visual Quality and Central Subfield Thickness
[1079] In general, no substantial increase in the mean CSFT was
observed for the subjects of cohort 1 over the 9-month study
duration (FIG. 17). In some subjects of cohort 1, a reduction of
CSFT was observed with the 200 .mu.g dose. Subject #1 from cohort 1
(naive) showed a significant reduction in CSFT in the study eye
from 1252 .mu.m (baseline value at day 1) to 936 .mu.m (after 10.5
months), while visual acuity (referring to the clarity of vision)
was not impaired in the study eye (FIG. 16). No rescue therapy was
needed throughout the study duration of subject #1 (10.5 months).
Mean visual acuity (BCVA) was not significantly impaired in the
patients of cohort 1 (FIG. 18), meaning that BCVA was still within
15 ETDRS letters from baseline (determined prior to administration
of the implant).
[1080] The mean central subfield thickness (CSFT) was reduced for
the subjects from cohort 2 over 14 months (FIG. 17). Moreover, mean
visual acuity (BCVA) was not significantly impaired in the patients
of cohort 2 (FIG. 18).
[1081] FIGS. 19 A and B, and FIG. 20 exemplarily show images from
SD-OCT evaluation of two subjects from cohort 2. Subject #1 from
cohort 2 had been treated with aflibercept for over a year (16
months) prior to injection of the axitinib implants in the right
eye (oculus dexter, OD). Subretinal fluid was clearly visible at
baseline (pre-treatment). Importantly, the sub-retinal fluid was
gone after 2-3 months after implant injection and this stage was
essentially maintained over the complete study duration of 15.5
months without rescue therapy (FIGS. 19 A and B). Up to month 12.5
two implants were visible, thereafter one implant was visible.
Subject #7 from cohort 2 had been treated with aflibercept for 6
years prior to implant administration. CSFT was efficiently reduced
from 335 .mu.m baseline through month 9 (e.g. CSFT of 271 .mu.m at
month 9) without rescue therapy (FIG. 20). At month 10 the CSFT
started to increase again. Two implants were present until month
12. Follow-up is ongoing.
[1082] In summary, the clinical data demonstrate efficacy and
implant persistence in the eye for up to about or even beyond 14
months in certain subjects. These observations have not been
expected. In the in vitro real-time release experiments the
complete axitinib dose was released after around 8 months (cf. FIG.
14A).
Plasma Concentration
[1083] Plasma concentrations of axitinib were below the lower limit
of quantification (LLOQ<0.1 ng/mL) at all samples time-points in
all subjects, indicating that administration of the implant(s) did
not lead to systemic drug exposure. This further validates the
overall safety of the axitinib implants of the present
application.
Tolerability and Adverse Events
[1084] In general, the treatment has been safe and well-tolerated.
Injection courses were uncomplicated for most of the subjects. FA
and OCT revealed no clinically significant leakage for any of the
subjects throughout the study duration. IOPs were normal
independent of the dose for all subjects over the study duration.
Inflammation was not observed for any of the subjects. No subjects
needed ocular steroids.
[1085] All reported adverse events were mild to moderate, no severe
adverse events or severe ocular adverse events were reported (Table
23).
TABLE-US-00031 TABLE 23 Adverse events reported for the cohorts 1
and 2. Cohort 1: Cohort 2: 200 .mu.g 400 .mu.g axitinib axitinib
Total Number of subjects with: (n = 6) (n = 7) n = 13 Adverse
Events (AEs) 14 22 36 Suspected relationship to 1 2 3 study product
Suspected relationship to 1 3 4 injection procedure Ocular AEs 12
15 27 Ocular AEs in Study Eye 7 13 20 Serious Ocular AEs 0 0 0 By
severity Mild 12 17 29 Moderate 2 5 7 Severe 0 0 0
[1086] Adverse events observed in the study eye included tiny
pigmented keratic precipitates (3/13), subconjunctival hemorrhage
following injection (3/13) and pain following injection (2/13).
Importantly, only 3 adverse events with suspected relationship to
the study product were reported. For example, one patient had
opacities around the implant, one patient hat vitreous floaters,
three patients had tiny pigmented keratic precipitates (no
treatment required), and one had foreign material (fiber and
reflective particles). Further specific adverse events are listed
in the following Table 2).
TABLE-US-00032 TABLE 24 Specific adverse events reported for the
study eye for the cohorts 1 and 2. Cohort 1: Cohort 2: 200 .mu.g
400 .mu.g axitinib axitinib Total Number of subjects with: (n = 6)
(n = 7) n = 13 Tiny Pigmented KPs 3 0 3 Opacities around OTX
Implant 1 0 1 Discomfort/Difficulty opening 1 0 1 eyes on waking
Dry eyes 1 0 1 Increased Geographic Atrophy 0 1 1 Pain 0 2 2
Vitreous Floaters 0 1 1 Corneal Scratch 0 1 1 Blepharitis 0 1 1
Subconjunctival Haemmorhage 1 2 3 TKI implant obstruction vision 0
1 1 Foreign material noted in vitreous 0 1 1 Worsen cataracts 0 1 1
Subconjunctival haemoatoma 0 0 0 Trace anterior chamber cells 0 0 0
Red eye 0 1 1 Watery eye 0 1 1 Eye discomfort 0 0 0 Foreign body
sensation 0 0 0 Small hair in vision 0 0 0
[1087] In summary, the axitinib implants of the present invention
were safe and well-tolerated. The implants showed efficient
reduction or showed essentially maintenance of CSFT versus the
baseline determined prior to administration of the implant.
Evaluation of 600 .mu.g Axitinib Dose and 400 .mu.g Axitinib Dose
with Anti-VEGF Co-Administration
[1088] To further explore efficacy of the implants in humans,
further clinical studies are ongoing with one cohort (cohort 3a) of
subjects suffering from wet AMD (planned: n=6) receiving three of
the 200 .mu.g implants (Table 21.1, Implant #1) as separate
injections resulting in a total axitinib dose of 600 .mu.g per eye,
as well as with another cohort (cohort 3b) of subjects suffering
from wet AMD (planned: n=6) receiving two of the 200 .mu.g implants
(Table 21.1, Implant #1) as separate injections resulting in a
total axitinib dose of 400 .mu.g per eye and in addition receiving
a single anti-VEGF injection (Avastin or EYLEA.RTM.), which is
administered during the same session as the placement of the
implants. One eye per patient is treated.
[1089] For cohort 3a, all 6 subjects have started treatment and are
currently being treated, for cohort 3b, 2 subjects from the planned
number of 6 subjects have started treatment and are currently being
treated. Two out of the 8 currently treated subjects are female, 6
are male. The baseline CSFT for the 8 currently treated subjects in
cohort 3 is 518.+-.53 .mu.m (mean.+-.SE), and the baseline BCVA
(Snellen equivalent) is 0.88.+-.0.12 (mean.+-.SE). In general,
implants exhibited limited movement in the vitreous. An overview of
the subjects enrolled to date in cohorts 3a and 3b is provided in
Table 25. Overview charts presenting summary data regarding central
subfield thickness (CSFT) and best corrected visual acuity (BCVA)
of all subjects enrolled and analyzed so far in cohorts 3a and 3b
are provided in FIGS. 17 and 18, respectively. In addition, in
order to exemplary illustrate the course of CSFT and BCVA in
subjects of cohorts 3a and 3b, certain specific subjects are
discussed herein in more detail, and images showing the CSFT and
BCVA in these subjects at exemplary visits are provided in the
Figures. These exemplary subjects are discussed to illustrate CSFT
and BCVA measurement and development in subjects/patients who
participated in the study, but are singular subjects. For the mean
change of CSFT and BCVA over all subject of cohorts 3a and 3b, it
is referred to FIGS. 17 and 18. For the charts in these FIGS. 17
and 18: Six patients were followed in cohort 3a until day 14, five
until month 2, two until month 4.5, and one until months 6 and 7.5.
Two patients were followed in cohort 3b until month 3, and one
until month 4.5. Follow-up is ongoing.
TABLE-US-00033 TABLE 25 Overview of subjects from the two cohorts
(cohort 3a and 3b). Age, Sex (male M, female F), together with
prior treatment and study eye are presented. For the study eye
(oculus dexter, (OD) or oculus sinister (OS)), treatment BCVA is
given as logMAR (logarithm of the minimal pre-angle resolution) and
Snellen equivalent. A conversion chart from EDTS letter score to
LogMAR value and Snellen equivalent can be found in Beck et al., Am
J Ophthalmol 2003, 135:194-205. In addition, CSFT pre-treatment is
presented. All pre-treatment results are from day 1 of the study.
Study Eye Pre- Pre- Treatment Treatment Pre- Subject logMAR Snellen
Treatment No. Age Sex Prior Treatment Study Eye BCVA BCVA CSFT
(.mu.m) Cohort 3a (600 .mu.g) #1 79 M Naive OS 0.58 20/76 484 #2 84
M Naive OD 0.70 20/100 551 #3 72 M Naive OD 0.32 20/42 481 #4 70 M
Anti-VEGF OS 1.04 20/219 825 #5 78 F Naive OS 1.1 @ 1 m 20/252 320
#6 84 M Naive OD 1.1 20/252 466 Cohort 3b (400 .mu.g + anti-VEGF)
#1 71 M Naive OD 0.88 @ 1 m 20/152 423 #2 80 F Anti-VEGF OS 1.34 @
1 m 20/438 559
Visual Quality and Central Subfield Thickness
[1090] The first patient of cohort 3a (3.times.200 .mu.g implant)
is a 79 year-old male, who is naive for AMD treatment. The
injection course was uncomplicated. The implants were placed over
one week (on days 1 (baseline) and 7) in the left eye (OS).
Notably, CSFT was efficiently reduced over the first 7.5 months
while BCVA remained unaffected (FIG. 21). The second patient of
cohort 3a (3.times.200 .mu.g implant; not shown in the Figures) is
an 84 year-old male, who is naive for treatment. The injection
course was uncomplicated. The three implants were placed all in one
day (day 1, baseline). CSFT was essentially stabilized for 4.5
months, i.e., did not clinically significantly increase. Follow-up
is ongoing.
[1091] Generally, mean CSFT was greatly reduced at 6 months after
insertion of the implants in patients of cohort 3a (FIG. 17). Mean
BCVA increased markedly for cohort 3a after 3 months (FIG. 18).
[1092] The first patient of cohort 3b (2.times.200 .mu.g implant
and anti-VEGF) is a 71 year old male, who is naive for AMD
treatment. The injection course was uncomplicated. The implants and
the anti-VEGF injection were all placed on day 1 (baseline) in the
right eye (OD). Already after 7 days a clear reduction in CSFT was
visible while BCVA was not affected. The CSFT was further reduced
and then essentially maintained over a 3 month treatment period,
and started to increase at month 4.5 (FIG. 22). The second patient
of cohort 3b had received anti-VEGF therapy for 7 months prior to
insertion of the implants. Even after a short treatment period of
only 7 days the CSFT was reduced by 2/3 (599 .mu.m at baseline and
188 .mu.m at day 7), while BCVA was not affected (FIG. 23). A low
CSFT value was maintained through month 2, but started to increase
at month 3. The subject received rescue therapy at month 4.5.
Follow-up is ongoing.
[1093] Mean CSFT was efficiently reduced during the first 3 months
after insertion of the implants in patients of cohort 3b (FIG. 17).
Mean BCVA slightly increased (FIG. 18).
Tolerability and Adverse Events
[1094] In general, also the implants in cohort 3a and 3b have been
safe and well-tolerated. Injection courses were uncomplicated for
most of the subjects. IOPs were normal independent of the dose for
all subjects over the study duration. Inflammation was not observed
for any of the subjects. No subjects needed ocular steroids.
[1095] All reported adverse events were mild, no moderate or severe
(ocular) adverse events were reported (Table 26.1). Importantly,
only one adverse event with suspected relationship to study product
was reported so far (see Table 26.1). Specific adverse events are
reported in Table 26.2. Follow-up is ongoing for cohorts 3a and
3b.
TABLE-US-00034 TABLE 26.1 Adverse events reported for cohorts 3a
and 3b (follow-up ongoing). Cohort 3b: Cohort 3a: 400 .mu.g 600
.mu.g axitinib + axitinib Anti-VEGF Total Number of subjects with:
(n = 6) (n = 2) n = 8 Adverse Events (AEs) 14 3 17 Suspected
relationship to 1 0 1 study product Susptected relationship to 9 2
11 injection procedure Ocular AEs 12 2 14 Ocular AEs in Study Eye
10 2 12 Serious Ocular AEs 0 0 0 By severity Mild 14 3 17 Moderate
0 0 0 Severe 0 0 0
TABLE-US-00035 TABLE 26.2 Specific adverse events reported for the
study eye for cohorts 3a and 3b so far (follow-up ongoing). Cohort
3b: Cohort 3a: 400 .mu.g 600 .mu.g axitinib + axitinib anti-VEGF
Total Number of subjects with: (n = 6) (n = 2) n = 8 Tiny Pigmented
KPs 0 0 0 Opacities around OTX Implant 0 0 0 Discomfort/Difficulty
opening 0 0 0 eyes on waking Dry eyes 0 0 0 Increased Geographic
Atrophy 0 0 0 Pain 2 1 3 Vitreous Floaters 0 0 0 Corneal Scratch 0
0 0 Blepharitis 0 0 0 Subconjunctival Haemmorhage 3 1 4 OTX Implant
obstruction vision 0 0 0 Foreign material note in vitreous 0 0 0
Worsen Cataracts 0 0 0 Subjconjunctival Haemoatoma 1 0 1 Trace
anterior chamber cells 1 0 1 Red eye 0 0 0 Watery eye 0 0 0 Eye
discomfort 1 0 1 Foreign body sensation 1 0 1 Small hair in vision
1 0 1
[1096] Alternatively, instead of three implants providing a total
dose of 600 .mu.g, one implant comprising a dose of 600 .mu.g
axitinib may be injected. Of note, injection of a 600 .mu.g bolus
dose in rabbits (cf. Example 3.6) did not result in significant
tissue changes and inflammatory responses were normal. Formulation
and dimension of 600 .mu.g implants suitable for use in clinical
studies are presented in Table 21.2.
Rescue Medication
[1097] If needed, according to the study protocol reproduced above
any subject in any of cohorts 1, 2, 3a and 3b has received rescue
therapy (an anti-VEGF agent, specifically an intravitreal injection
of 2 mg aflibercept) at the investigator's discretion. The
following criteria were used to identify subjects who would likely
require rescue therapy: [1098] loss of .gtoreq.15 letters from best
previous BCVA due to AMD, with current BCVA not better than
baseline; or [1099] loss of .gtoreq.10 letters on 2 consecutive
visits from best previous BCVA due to AMD, with current BCVA score
not better than baseline; or [1100] evidence of worsening disease
activity manifest by greater than 75 microns CSFT from previous
best value.
[1101] Not more than 50% of the subjects from cohorts 1, 2, 3a, and
3b required rescue medication as defined herein in the form of an
anti-VEGF treatment within the first 6 months after start of
treatment (implant injection) so far (Table 27). For instance, in
cohort 2 71.4% of the subjects did not receive rescue medication at
3 months after implant insertion, and 6 months after implant
insertion 57.1% of subjects did not receive rescue medication. Even
after a long treatment period of 11 or 13.5 months in cohort 2,
rescue medication was not needed for 28.6% or for 20% of the
subjects, respectively (especially in cohorts 3a and 3b the studies
are still ongoing). This low percentage of subjects needing rescue
medication demonstrates that the therapeutic effect of a reduction
of fluid achieved by the implants of the invention is maintained,
and the patients are stabilized at the reduced fluid state for an
extended period of time, such as for at least 3 months, at least 6
months, at least 9 months or at least 12 months. Specifically, the
data of cohorts 1 and 2 (200 .mu.g and 400 .mu.g axitinib,
respectively) in Table 27 show that the level of fluid in patients
that had been achieved by the administration of the implants could
be maintained in the period from 6 to 9 months without any need for
rescue medication, while vision (expressed by means of the BCVA)
was not significantly impaired (see FIG. 18).
TABLE-US-00036 TABLE 27 Percentage of subjects from all cohorts who
did not require rescue therapy. At 7.5 At 11 At 13.5 At 3 months At
6 months months At 9 months months months At 15.5 months Cohorts %
(n/N) % (n/N) % (n/N) % (n/N) % (n/N) % (n/N) % (n/N) Cohort 1 66.7
50 50 (3/6) 50 (3/6) NA NA NA (200 .mu.g) (4/6) (3/6) Cohort 2 71.4
57.1 42.9(3/7) 42.9 28.6 20 20 (1/5)* (400 .mu.g)* (5/7) (4/7)
(3/7) (2/7) (1/5)* Cohort 3a 100 100 100 TBD TBD TBD TBD (600
.mu.g)* (3/3)* (1/1)* (1/1)* Cohort 3b 100 TBD TBD TBD TBD TBD TBD
(400 .mu.g + (2/2)* anti- VEGF)* * = follow-up is ongoing. TBD = to
be determined. Note: in cohort 3a, one subject received rescue
medication at month 1, however this is not yet reflected in Table
27 as of the total of six subjects in cohort 3a only three already
reached 3 months, and none of these three had received rescue
medication (the subject having received rescue mediaction at month
1 has not yet reached month 3).
[1102] The doses of axitinib in implants applied in humans (200-600
.mu.g) are markedly lower compared to the approved INLYTA.RTM. dose
(2.times.5 mg/day). Even if an entire 600 .mu.g axitinib dose would
be delivered systemically at one time, this would nevertheless
allow a more than 15-fold safety margin of this full dose compared
to the daily INLYTA.RTM. dose, further underlining the safety of
the implants.
[1103] The above results demonstrate that the implants of the
present invention administered to patients diagnosed with
neovascular AMD were able to stabilize retinal fluid in these
patients (i.e., to either reduce, maintain or at least not
significantly increase retinal fluid) as evidenced by the CSFT,
while not impairing the patients' vision as evidenced by the BCVA,
for a treatment period of about 6 to about 9 months or even longer,
and that the implants were well tolerated.
Example 6.5: Proposed Human Clinical Trial with a 600 .mu.g
Axitinib Implant
[1104] The proposed study is a prospective, multi-center,
double-masked, randomized, parallel-group study to evaluate the
efficacy and safety of OTX-TKI (600 .mu.g axitinib implant) for
intravitreal use in subjects with previously treated neovascular
age-related macular degeneration (nAMD). The study objective is to
evaluate the efficacy and safety of OTX-TKI (0.6 mg axitinib
implant) for intravitreal use in previously treated patients with
neovascular age-related macular degeneration (AMD).
[1105] The primary efficacy endpoint will be: [1106] Mean change in
BCVA from baseline to 7 months
[1107] The secondary efficacy endpoints will be: [1108] Mean change
in BCVA from baseline over time at all study visits [1109] Mean
change in central subfield thickness (CSFT) from baseline over time
measured by SD-OCT at 7 months and all study visits and percent of
subjects with no increase in CSFT .gtoreq.50 .mu.m at all study
visits compared to baseline through Month 12 [1110] Proportion of
subjects with absence of retinal fluid (CSFT .ltoreq.300 .mu.m on
SD-OCT) at all study visits through Month 12, proportion of
subjects with no clinically significant increase in leakage from
baseline determined by FA at 7 months and all study visits,
proportion of patients with absence of fluid by fluid type
(subretinal fluid (SRF) or Intraretinal fluid (IRF); CSFT
.ltoreq.300 .mu.m on SD-OCT) at all study visits [1111] Proportion
of subjects receiving rescue therapy, mean time to rescue therapy,
and mean number of rescue therapy injections through Month 4, 7,
and 12.
[1112] Safety endpoint will be: [1113] Incidence of treatment
emergent adverse events (AEs) [1114] Vital signs changes over time
[1115] Ocular Comfort Score changes over time [1116] Clinically
relevant vision loss defined as a 6-line loss in vision compared to
baseline over time [1117] Clinically significant change in ocular
examination compared to baseline assessments (e.g., slit lamp
biomicroscopy, fundus exam, and IOP) over time.
[1118] Approximately 100 subjects of age 50 will be enrolled and
treated with 0.6 mg OTX-TKI (intravitreal implant) or 2 mg
aflibercept (intravitreal injection). Following confirmation of
eligibility at Visit 1 (Screening/Baseline), the subjects will be
randomized 1:1 to one of two groups. Subjects randomized to OTX-TKI
will receive a single injection of 0.6 mg OTX-TKI (0.6 mg
axitinib), and subjects randomized to aflibercept will receive a
sham (i.e., vehicle only) injection. At Visit 2 (Month 1) subjects
randomized to OTX-TKI will receive a single injection of 2 mg
aflibercept and subjects randomized to aflibercept will receive a
single injection of 2 mg aflibercept (i.e., all subjects will
receive an injection of 2 mg aflibercept at Visit 2/Month 1).
Subsequently, subjects randomized to the aflibercept group will
receive a single injection of 2 mg aflibercept every two months and
subjects randomized to the OTX-TKI group will receive a sham
injection every two months. The planned study design is shown in
FIG. 28.
[1119] The study population will be subjects with a diagnosis of
previously treated subfoveal neovascularization (SFNV) secondary to
neovascular AMD with leakage involving the fovea who received their
most recent anti-VEGF injection within the prior 1-4 weeks.
Example 7: Inflammation Study with Various TKIs
[1120] TKI sample preparation: Hydrogels containing several TKIs
were prepared for tolerability testing in rabbit eyes: sunitinib
axitinib, nintedanib and regorefanib. First, a diluent solution of
80% Provisc (Alcon, Inc.) and 20% of a 0.5 mg/mL sodium borate
solution (pH 6.8) was prepared. Next, mixtures containing 9.6% API,
77.8% diluent, 8.4% 4a20kPEG SAZ and 4.2% 8a20kPEG NH2 were
prepared. Prior to gelation, which occurred between 3.5 to 8
minutes after mixing, 10 .mu.L was injected intravitreally in New
Zealand white rabbit eyes using a Hamilton syringe.
[1121] Study Design: Briefly, on Day 0 rabbits were injected in the
left and right eye with test articles as listed below in the study
design table. Animals were euthanized at 2 weeks. Eyes were
harvested, and fixed in Davidson's solution for histopathologic
analysis.
TABLE-US-00037 TABLE 28 List of TKIs used in the inflammation
study. Treatment Group (OU) Endpoint 1 Sunitinib Histopathology 2
Nintedanib Histopathology 3 Regorefanib Histopathology 4 Axitinib
Histopathology 5 Sham Histopathology
[1122] Tissues examined: A total of 10 left and right eyes from 5
rabbits were submitted to Mass Histology and trimmed by a
board-certified veterinary pathologist.
[1123] Conclusion: Under the conditions of the study intravitreal
injection of rabbit eyes with formulations of hydrogel depots with
tyrosine kinase inhibitors at 14 days post-injection resulted in
the continued presence of the hydrogel in the vitreous chamber of
at least one eye from each group except Group 1 and Group 3 where
no hydrogel material was noted in either eye.
[1124] Inflammation was never present around any of the injected
material observed in any of the eyes from Groups 2, 4, and 5.
Minimal inflammation composed primarily of macrophages in the
vitreous chamber and/or attached to the retina was observed in
occasional samples from Groups 1 and 3. Again, no injected material
was observed in either eye from Group 1 or Group 3.
[1125] Minimal inflammation and fibrosis were observed in a few
slide samples from Groups 3 and 4. These were typically small
linear areas of fibrosis with a few macrophages admixed. They are
interpreted as sequela to needle injection.
[1126] One or a few small areas of retinal disruption or retinal
folds were observed in at least 1 eye from Groups 1, 3, 4 and 5.
These could be retinal invaginations due to needle injection. A
very small retinal detachment measuring 100 microns in length is
present in one eye at the location of the small retinal disruption
(Group 3). No other retinal detachments were noted in any eye from
any group.
[1127] A focus of mild histiocytic and multi-nucleated inflammation
was observed around a small displaced focus of lens fibers in the
vitreous chamber of one eye from Group 3. This is considered
lens-induced granulomatous endophthalmitis, and may be due to a
slight nick of the lens by the needle at injection. No other such
lesions were observed in any eye from any group.
Example 8: Additional Examples
[1128] In certain embodiments, the present invention also relates
to implants as disclosed herein that contain a high amount of TKI
such as axitinib, such as a dose of axitinib of more than about
1200 .mu.g, or more than about 1800 .mu.g. Certain exemplary
prophetic implants containing such a high dose of axitinib are
disclosed in the following Table 29.
TABLE-US-00038 TABLE 29 Prophetic implants containing a high dose
of axitinib (i.e., above 1200 .mu.g) Implant type Implant #1
Implant #2 Implant #3 Implant #4 Formulation Axitinib 68.6% 68.6%
68.6% 68.6% (% dry Dose 1580 ug 2360 ug 6010 ug 8990 ug basis w/w)
PEG Hydrogel 26.0% 26.0% 26.0% 26.0% 4a20K PEG-SAZ 17.4% 17.4%
17.4% 17.4% 8a20K PEG-NH2 8.7% 8.7% 8.7% 8.7% Sodium phosphate 5.4%
5.4% 5.4% 5.4% Formulation Axitinib 16.5% 16.5% 16.5% 16.5% (% wet
PEG Hydrogel 6.3% 6.3% 6.3% 6.3% basis w/w) 4a20K PEG-SAZ 4.2% 4.2%
4.2% 4.2% 8a20K PEG-NH2 2.1% 2.1% 2.1% 2.1% Sodium phosphate 1.3%
1.3% 1.3% 1.3% WFI 75.9% 75.9% 75.9% 75.9% Axitinib per final dry
145.0 ug/mm 145.0 ug/mm 551.4 ug/mm 551.4 ug/mm length Approximate
Implant 2303 3440 8761 13105 Mass (dose ug/API %) Configuration
Stretching Method Wet Wet Wet Wet (Stretch Factor) (2.1) (2.1)
(2.1) (2.1) Needle Size 22G ETW 22G ETW 17G ETW 17G ETW (0.522 mm
ID) (0.522 mm ID) (1.24 mm ID) (1.24 mm ID) Injector/Syringe
Implant Implant Implant Implant Injector Injector Injector Injector
Packaging Foil Pouches Foil Pouches Foil Pouches Foil Pouches
Sterilization Type Gamma Gamma Gamma Gamma Site Storage
Refrigerated Refrigerated Refrigerated Refrigerated Dimensions
Dried Diameter 0.49 mm 0.49 mm 0.97 mm 0.97 mm Length 10.9 mm 16.3
mm 10.9 mm 16.3 mm Volume 2.1 mm.sup.3 3.1 mm.sup.3 8.0 mm.sup.3
12.0 mm.sup.3 Implant Mass 2.3 mg 3.4 mg 8.8 mg 13.1 mg Hydrated
Diameter 1.0 mm 1.0 mm 2.0 mm 2.0 mm Length 10.0 mm 15.0 mm 10.0 mm
15.0 mm
* * * * *