U.S. patent application number 14/897439 was filed with the patent office on 2016-05-12 for modified release formulation.
The applicant listed for this patent is Bruno GALLI, Jean-Marie GLANTZMANN, Arnaud GRANDEURY, Klaus-Peter MOLL, Martin MUELLER-ZSIGMONDY, Karsten PUTZBACH, Dirk SPICKERMANN, Hubert THOMA, Mike UFER. Invention is credited to Bruno GALLI, Jean-Marie GLANTZMANN, Arnaud GRANDEURY, Klaus-Peter MOLL, Martin MUELLER-ZSIGMONDY, Karsten PUTZBACH, Dirk SPICKERMANN, Hubert THOMA, Mike UFER.
Application Number | 20160128979 14/897439 |
Document ID | / |
Family ID | 51211272 |
Filed Date | 2016-05-12 |
United States Patent
Application |
20160128979 |
Kind Code |
A1 |
THOMA; Hubert ; et
al. |
May 12, 2016 |
MODIFIED RELEASE FORMULATION
Abstract
Drug products in the form of modified release formulations
comprising the drug substance
(-)-(3aR,4S,7aR)-4-Hydroxy-4m-tolylethynyl-octahydro-indole-1-carboxylic
acid methyl ester (AFQ056), as well as processes for making such
drug products are provided. The drug products are useful in
treating patients with Parkinson's disease and exhibiting L-dopa
induced dyskinesia.
Inventors: |
THOMA; Hubert;
(Pfaffenweiler, DE) ; GALLI; Bruno; (Seltisberg,
CH) ; SPICKERMANN; Dirk; (Staufen, DE) ;
PUTZBACH; Karsten; (Basel, CH) ; MOLL;
Klaus-Peter; (Basel, CH) ; UFER; Mike;
(Allschwil, CH) ; GRANDEURY; Arnaud;
(Helfrantzkirch, FR) ; GLANTZMANN; Jean-Marie;
(Michelbach-Le-Bas, FR) ; MUELLER-ZSIGMONDY; Martin;
(Freiburg, DE) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
GALLI; Bruno
THOMA; Hubert
GRANDEURY; Arnaud
SPICKERMANN; Dirk
PUTZBACH; Karsten
MOLL; Klaus-Peter
UFER; Mike
GLANTZMANN; Jean-Marie
MUELLER-ZSIGMONDY; Martin |
Basel
Basel
Basel
Stein
Basel
Basel
Basel
Basel
Basel |
|
CH
CH
CH
CH
CH
CH
CH
CH
CH |
|
|
Family ID: |
51211272 |
Appl. No.: |
14/897439 |
Filed: |
June 11, 2014 |
PCT Filed: |
June 11, 2014 |
PCT NO: |
PCT/IB2014/062136 |
371 Date: |
December 10, 2015 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
61834104 |
Jun 12, 2013 |
|
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|
Current U.S.
Class: |
424/465 ;
424/489; 424/490; 514/412 |
Current CPC
Class: |
A61P 25/16 20180101;
A61P 25/04 20180101; A61P 25/32 20180101; A61K 9/5089 20130101;
A61J 3/10 20130101; A61K 9/2004 20130101; A61J 3/02 20130101; A61K
9/28 20130101; A61K 9/2072 20130101; A61K 9/50 20130101; A61K
31/404 20130101; A61K 47/38 20130101; A61P 25/00 20180101; A61P
25/14 20180101; A61P 25/36 20180101; A61K 31/4045 20130101; A61K
9/1682 20130101; A61P 25/28 20180101; A61P 25/34 20180101; A61P
25/30 20180101; A61K 9/1652 20130101; A61P 25/24 20180101 |
International
Class: |
A61K 31/404 20060101
A61K031/404; A61K 9/16 20060101 A61K009/16; A61J 3/02 20060101
A61J003/02; A61K 9/20 20060101 A61K009/20; A61J 3/10 20060101
A61J003/10; A61K 47/38 20060101 A61K047/38; A61K 9/50 20060101
A61K009/50 |
Claims
1. A stable modified release formulation comprising
(--)-(3aR,4S,7aR)-4-Hydroxy-4m-tolylethynyl-octahydro-indole-1-carboxylic
acid methyl ester in free base form as active pharmaceutical
ingredient and a modified release agent, such that the active
pharmaceutical ingredient is released from the formulation in a
controlled fashion over a period of 6 hours, or over a period of 7
hours, so that at least 80% of the active pharmaceutical ingredient
has been released at the end of this period.
2. The modified release formulation according to claim 1 having the
following release characteristics in water: about 14% to about 20%
after 60 minutes; about 51% to about 61% after 180 minutes; about
67% to about 77% after 240 minutes; about 90% to about 95% after
360 minutes; and about 95% to about 99% after 420 minutes. The
before mentioned release characteristics are obtained by using
standard dissolution rate equipment (paddle according to e.g. USP)
at 100 rpm with 900 ml of Water+0.5% LDAO.
3. The modified release formulation according to claim 1, wherein
the modified release agent is hydroxy propyl methylcellulose.
4. The modified release formulation according to claim 3 wherein
the drug substance has a particle size distribution of
x10.ltoreq.50 .mu.m, x50.ltoreq.100 .mu.m and x90.ltoreq.200
.mu.m.
5. The modified release formulation according to claim 4 that
exhibits a similar or decreased release rate in ethanol containing
media as compared to a aqueous media with 0.5% LDAO.
6. The modified release formulation according to claim 1 further
comprising a coating.
7. The modified release formulation according to claim 1 in form of
a single unit dosage form comprising about 25 mg to about 250 mg
(--)
-(3aR,4S,7aR)-4-Hydroxy-4m-tolylethynyl-octahydro-indole-1-carboxylic
acid methyl ester in free base form, about 69 mg to about 135 mg
hypromellose (type 2208 characterized by viscosities between about
80 to about 120 cP (20.degree. C.)), about 20 mg to about 160 mg
lactose monohydrate, about 3 mg to about 38 mg sodium starch
glycolate, about 2 mg to about 4.5 mg Magnesium stearate and about
1 mg to about 2.2 mg colloidal silicon dioxide.
8. The modified release formulation according to claim 7 wherein
(--)-(3aR,4S,7aR)-4-Hydroxy-4m-tolylethynyl-octahydro-indole-1-carboxylic
acid methyl ester in free base form is present in an amount of
about 25 -250 mg.
9. The modified release formulation according to claim 1 in single
unit dosage form comprising equal to or less than 100 mg AFQ056
compressed to round tablets with a diameter of about 8 mm.
10. The modified release formulation according to claims 1 in
single unit dosage form comprising more than 100 mg AFQ056
compressed to round tablets with a diameter of about 11 mm.
11. A process for the production of a modified release formulation
of claim 1, comprising (i) mixing AFQ056 with filler, binder and
disintegrant in a high shear granulator (ii) adding purified water
under mixing (iii) kneading the mixture in a high shear granulator
(iv) passing the granulate through a screen using a screening mill
(v) drying the granulate in a fluid bed dryer (vi) mixing the dry
granulate with a modified release agent, filler and glidant
followed by consecutive sieving using screening mill and mixing in
a diffusion mixer (vii) sieving a lubricant and adding to the
mixture from the diffusion mixer (viii) forming the composition
12. The modified release formulation according to claim 1 for use
in the treatment of Parkinson's disease L-dopa induced dyskinesia,
Fragile X syndrome (Martin-Bell syndrome), dyskinesia in Fragile X
syndrome, obsessive compulsory disorders, autism, cystitis, and for
the treatment, prevention or delay of progression of acute,
traumatic and chronic degenerative processes of the nervous system,
such as Parkinson's disease, senile dementia, Alzheimer's disease,
Huntington's chorea, amyotrophic lateral sclerosis and multiple
sclerosis, psychiatric diseases such as schizophrenia and anxiety,
depression, pain, itch and drug abuse such as alcohol and nicotine
abuse and cocaine use disorders.
Description
BACKGROUND OF THE INVENTION
[0001] The drug substance AFQ056 is a subtype-selective,
non-competitive antagonist at the metabotropic glutamate receptor 5
(mGluR5). Glutamate is the main excitatory neurotransmitter in the
nervous system and as such is involved in a variety of
physiological and pathophysiological functions. Excessive
glutamatergic transmission has been shown to play a role in both
movement disorders and psychiatric conditions and the
pharmacological use of glutamate receptor antagonists has shown
efficacy in these indications.
[0002] The systemic chemical name for AFQ056 is
(-)-(3aR,4S,7aR)-Octahydro-4-hydroxy-4-[(3-methylphenyl)ethynyl]-1H-indol-
e-1-carboxylic acid methyl ester, and is also known as
(-)-(3aR,4S,7aR)-4-Hydroxy-4m-tolylethynyl-octahydro-indole-1-carboxylic
acid methyl ester. AFQ056 has the molecular formula
C.sub.19H.sub.23NO.sub.3 and the following structural formula:
##STR00001##
[0003] AFQ056 drug substance is a white to practically white
powder, which is hardly soluble in water but soluble in organic
solvents (distribution coefficient is Log P=4.7). AFQ056 is a
chiral molecule with 3 asymmetric carbon atoms and has a melting
point of about 115.degree. C. One single polymorph has been
identified.
[0004] WO 03/047581 describes the preparation of AFQ056 and its use
as a pharmaceutical, especially in the treatment of nervous system
disorders including Parkinson's disease. Parkinson's disease (PD)
is a degenerative movement disorder that affects approximately
100-250 cases per 100,000 individuals. Treatment with L-dopa, a
precursor of dopamine, constitutes the mainstay and gold standard
in the treatment of PD. One of the major problems associated with
long-term L-dopa treatment is the development of L-dopa induced
motor complications such as dyskinesias (LIDs).
[0005] AFQ056 has previously been formulated as a hard gelatin
capsule and as a powder for oral suspension, both with immediate
release (IR) properties. Results in Parkinson's disease patients
administered AFQ056 demonstrate a reduction in L-dopa induced
dyskinesias without inducing any clinically or statistically
significant worsening of the underlying Parkinsonian motor
symptoms. The most frequent adverse events observed in patients are
in the nervous system and psychiatric system organ class, including
dizziness, dyskinesia, nausea, fatigue, and hallucinations. Results
also revealed that a significant proportion of patients did not
achieve and maintain the target dose throughout the study,
presumably due to tolerability issues such as dizziness. The IR
formulation used in these studies required twice-daily dosing.
[0006] Advantages of modified release formulations are the
prolonged blood plasma levels of drug compared to an immediate
release formulation. Modified release formulations usually contain
more of the drug than the single dose administered in an immediate
release dose form. If the formulation releases the drug at a rate
that is faster than the intended controlled release rate (often
referred to as dose dumping), there is a risk of overdosing with
potential severe consequences for the patient.
[0007] An additional safety concern can occur where the drug may
interact with alcohol (ethanol) and lead to changes in the
pharmacokinetic pattern. Oral formulations are often taken with a
commonly available beverage such as water, carbonated beverage etc.
or occasionally with an alcohol-containing (ethanol-containing)
beverage. Dose dumping needs to be prevented also when the patient
consumes alcoholic beverages hours after ingestion of the modified
release formulation. Dose dumping needs to be prevented also when
patients desire to abuse a drug due to its inherent side effects,
like hallucinations etc.
[0008] U.S. 2003/0118641 relates to abuse-resistant sustained
release opioid formulations using an ionic exchange resin. WO
2008/086804 describes the preparation of pharmaceutical
compositions comprising polyglycols that mitigate the risk of
alcohol induced dose dumping and that reduce the risk of drug
abuse. U.S. 2008/0085305 refers to robust sustained release
formulations based on hydrophilic gums that resist dose dumping
when ingested with alcohol. Roberts et al. (Int. Journal of
Pharmaceutics 2007, 332, p. 31-37) describe the influence of
ethanol on an oral dosage form comprising hypromellose matrices and
aspirin. To the best of the inventors' knowledge no modified
release formulation has been developed that takes into account the
specificities of AFQ056 and at the same time eliminates the risk
for alcohol induced does dumping after co-ingestion.
[0009] Therefore, there is a need for a safe modified release
formulation, preferably a once daily dose, with a lowered Cmax/AUC
ratio relevant for tolerability, efficacy and compliance, thus
allowing more patients to be treated with clinically efficacious
doses of AFQ056. Furthermore, there is a need for a pharmaceutical
formulation that prevents drug abuse, in particular regarding a
concomitant consumption of alcoholic beverages.
SUMMARY OF THE INVENTION
[0010] The present invention provides drug products comprising
AFQ056 having modified drug substance release properties. In one
embodiment of the invention there is provided a modified release
formulation comprising
(-)-(3aR,4S,7aR)-4-Hydroxy-4m-tolylethynyl-octahydro-indole-1-carboxylic
acid methyl ester in free base form, and a modified release agent,
preferably hydroxy propyl methylcellulose (also known as
hypromellose), together with one or more pharmaceutically
acceptable excipients.
[0011] In one embodiment of the invention there is provided a
modified release formulation comprising
(-)-(3aR,4S,7aR)-4-Hydroxy-4m-tolylethynyl-octahydro-indole-1-carboxylic
acid methyl ester in free base form as active pharmaceutical
ingredient and a modified release agent, preferably hydroxyl propyl
methylcellulose, such that the active pharmaceutical ingredient is
released from the formulation in a controlled fashion over a period
of 6 hours, or over a period of 7 hours, so that at least 80% of
the active pharmaceutical ingredient has been released at the end
of this period.
[0012] The drug products in the form of modified release
formulations of the present invention release AFQ056 in a range of
from about 14% to about 20% after 60 minutes; about 51% to about
61% after 180 minutes; about 67% to about 77% after 240 minutes;
about 90% to about 95% after 360 minutes; and about 95% to about
99% after 420 minutes.
[0013] In another embodiment of the invention there is provided a
modified release formulation comprising
(--)-(3aR,4S,7aR)-4-Hydroxy-4m-tolylethynyl-octahydro-indole-1-carboxylic
acid methyl ester in free base form that exhibits a similar or
decreased release rate in ethanol containing media as compared to a
purely aqueous media.
[0014] The drug substance has a particle size distribution of
x10.ltoreq.50 .mu.m, x50.ltoreq.100 .mu.m and x90.ltoreq.200
.mu.m.
[0015] In one embodiment of the invention, the drug products of the
present invention are single unit dosage forms with AFQ056 present
in an amount of about 25 mg to about 250 mg. In a preferred
embodiment, AFQ056 is present in an amount of about 50 to about 200
mg, more preferably in an amount of about 75 to 150 mg, more
preferably in an amount of about 100 mg.
[0016] In another embodiment, the pharmaceutical composition
comprises a coating.
[0017] In a further embodiment a single unit dosage form is
provided comprising about 25 mg to about 250 mg AFQ056, about 69 mg
to about 135 mg hypromellose (type 2208 characterized by
viscosities between about 80 to about 120 cP (2% in water at
20.degree. C.)) about 20 mg to about 160 mg lactose monohydrate,
about 3 mg to about 38 mg sodium starch glycolate, about 2 mg to
about 4.5 mg Magnesium stearate and about 1 mg to about 2.2 mg
colloidal silicon dioxide.
[0018] In another embodiment, the drug product is a pharmaceutical
composition comprising
(--)-(3aR,4S,7aR)-4-Hydroxy-4m-tolylethynyl-octahydro-indole-1-carboxylic
acid methyl ester in the form of a single unit dosage form
comprising equal to or less than 100 mg AFQ056 compressed to round
tablets with a diameter of about 8 mm. In still another embodiment,
the drug product comprising AFQ056 is in the form of a single unit
dosage form comprising more than 100 mg AFQ056 compressed to round
tablets with a diameter of about 11 mm.
[0019] In another embodiment of the invention, there is provided a
process for the production of a composition comprising AFQ056 and
having modified release properties. The process comprises
[0020] (i) mixing AFQ056 with filler, binder and disintegrant in a
high shear granulator
[0021] (ii) adding purified water under mixing
[0022] (iii) kneading the mixture in a high shear granulator
[0023] (iv) passing the granulate through a screen using a
screening mill
[0024] (v) drying the granulate in a fluid bed dryer
[0025] (vi) mixing the dry granulate with a modified release agent,
filler and glidant in a diffusion mixer followed by consecutive
sieving and mixing
[0026] (vii) sieving a lubricant and adding to the mixture from
step (vi)
[0027] (viii) final mixing the mixture from step (vii) in a
diffusion mixer.
[0028] (ix) forming the composition.
[0029] In another embodiment of the invention there is provided the
use of a modified release formulation in the manufacture of a
medicament for the treatment of Parkinson's disease L-dopa induced
dyskinesia, Fragile X syndrome (Martin-Bell syndrome), dyskinesia
in Fragile X syndrome, obsessive compulsory disorders, autism,
cystitis, and for the treatment, prevention or delay of progression
of acute, traumatic and chronic degenerative processes of the
nervous system, such as Parkinson's disease, senile dementia,
Alzheimer's disease, Huntington's chorea, amyotrophic lateral
sclerosis and multiple sclerosis, diseases such as schizophrenia
and anxiety, depression, pain, itch and drug abuse such as alcohol
and nicotine abuse and cocaine use disorders.
[0030] Also provided is a method of treating a patient with
Parkinson's disease and exhibiting L-dopa induced dyskinesia, by
administering an effective amount of a pharmaceutical composition
of the present invention.
[0031] In another embodiment there is provided a method of treating
a patient with Parkinson's disease and exhibiting L-dopa induced
dyskinesia, which comprises administering to said patient an
effective amount of the drug product comprising AFQ056 with a
modified release profile of Cmax/AUC of about, 0.08 to about 0.18
and a Tmax of about 4 hours to about 6 hours.
BRIEF DESCRIPTION OF THE DRAWINGS
[0032] FIG. 1 shows the dissolution profiles and the in vivo-in
vitro correlation (IVIVC) of two modified release formulations and
of a formulation for a capsule (immediate release form 50 mg). The
calculated profiles are in line with the measured human plasma
concentrations. FIG. 1 shows the validity of the used prediction
model. The measured in-vitro profiles together with the model (not
shown) allow to predict the human profiles derived from the
in-vitro modified release and immediate release-formulation
dissolution data.
[0033] FIG. 2 graphically depicts the solubility of AFQ056 at
37.degree. C. in different aqueous media. FIG. 2 shows that raising
ethanol levels in the pure aqueous solution lead to a steadily
increasing solubility of AFQ056. Up to the amount of about 20% of
ethanol in the solutions, the LDAO (Lauryldimethylamine N-oxide) in
water solution and the water-ethanol solution show a different
solubility pattern of AFQ056. In the presence of about 40% ethanol
in the solutions, both the LDAO in water solution and the
water-ethanol solution show a similar solubility for AFQ056.
[0034] FIG. 3 shows the dissolution rate of the modified release
form. All modified release dosage strengths show consistently a
lower dissolution rate in the presence of 20% ethanol.
[0035] FIG. 4 graphically depicts the dissolution rates of the
modified release form and of the immediate release form in the
presence of ethanol, the latter consistently showing a trend to
faster dissolution rate in the presence of 20% and 40% Ethanol
which is expected from solubility at the respective ethanolic
concetrations.
[0036] FIG. 5 shows the dissolution profile of the immediate
release form (capsule) comprising 50 mg AFQ056. After about 30
minutes in the 0.5% LDAO in water solution containing 40% ethanol,
a dissolution of 100% is achieved. FIG. 5 shows also that in the
simulation of human PK parameters (simulation of human PK applying
the in-vitro in-vivo correlation model) the Tmax value in the
ethanol containing solution is achieved faster and the Cmax and the
AUC.sub.48h are both higher compared to the observed plasma
concentrations in study X2101.
[0037] FIG. 6 graphically depicts the dissolution profile of the
immediate release form (capsule) comprising 400 mg AFQ. After about
30 minutes in the LDAO in water solution containing 40% ethanol, a
dissolution of almost 100% is achieved. In the simulation of human
PK parameters (simulation of human PK applying the in-vitro in-vivo
correlation model) the Tmax value in the ethanol containing
solution is achieved faster and the Cmax and the AUC.sub.48h are
both higher compared to the observed plasma concentrations in study
X2101.
[0038] FIG. 7 graphically depicts the dissolution profile of the
modified release form comprising 200 mg AFQ056. After 8 hours in
the LDAO in water solution containing 40% ethanol, a dissolution of
less than 80% was observed. In the simulation of human PK
parameters (simulation of human PK applying the in-vitro in-vivo
correlation model) the Tmax value in the ethanol containing
solution is almost identical and the Cmax and the AUC.sub.48h are
both almost equal to the observed plasma concentrations in study
X2101.
[0039] FIG. 8 provides a comparative dissolution profile of AFQ056
modified release film-coated tablets studied in a human experiment.
It is shown that the modified release tablets release the active
pharmaceutical ingredient in a controlled fashion almost linearly
during several hours. At the end of a period of 6 hours, or at the
end of a period of 7 hours, at least 80% of the active
pharmaceutical ingredient has been released.
[0040] FIG. 9 graphically depicts mean (SD) plasma
concentration-time profiles of modified release forms compared with
a capsule immediate release form, under fasted and fed
conditions.
[0041] FIG. 10 graphically depicts mean (SD) plasma
concentration-time profile of a selected modified release
formulation B under fasted versus fed conditions.
[0042] FIG. 11 graphically depicts percent AFQ056 drug substance
dissolved after 45 minutes versus AFQ056 drug substance particle
size x90 value (90% of the particles are smaller or equal).
DETAILED DESCRIPTION OF THE INVENTION
[0043] The present invention provides drug products in the form of
modified-release formulations of AFQ056, which alter the
pharmacokinetic profile of AFQ056, resulting in effective and
sustained drug concentration over a longer period of time, reducing
the peak to trough ratio. The modified release formulations of the
present invention have a positive food effect with increased Cmax
compared to the fasted state.
[0044] A modified release form is a solid oral dosage form that
permits the release of the active ingredient over an extended
period of time to maintain therapeutically effective plasma levels.
The modified release formulation may be a controlled release
formulation, one that exhibits substantially zero order release
kinetics. It may also be a sustained release formulation, which
exhibits first order kinetics.
[0045] An immediate release form is a solid oral dosage form that
permits the release of most or all of the active ingredient over a
short period of time, such as 60 minutes or less, and make rapid
absorption of the drug possible.
[0046] Dose dumping is an unintended, rapid drug release in a short
period of time of the entire amount or of a significant fraction of
the active drug substance retained in a release dosage form.
[0047] The solubility pattern of AFQ056 was examined (FIG. 1).
AFQ056 is hardly soluble in water but soluble in organic solvents
such as ethanol. In pure aqueous solutions the solubility of AFQ056
steadily increases with raising ethanol concentrations. The
solubility pattern of AFQ056 in a LDAO water-ethanol solution is
distinct from the solubility pattern of AFQ056 in a pure aqueous
solution only up to an amount of 20% ethanol present in the
solution. It was observed that the increase in solubility of AFQ056
by raising the presence of ethanol is even steeper than the
solubility of a comparable drug such as aspirin (Roberts et al.;
Int. Journal of Pharmaceutics 2007, 332, p. 31-37). Solubilities of
AFQ056 are about 0.02 mg/ml in water and raise up to about 53 mg/ml
(factor 2500x solubility increase) in ethanol at room temperature.
This is in contrast to 8.4 mg/ml for Aspirin in water raising up to
about 237 mg/ml in ethanol (factor 28x solubility increase). It was
observed that high concentrations of ethanol significantly raise
the dissolution rate and thus have an impact on the pharmacokinetic
parameters. FIGS. 5 and 6 show that the predicted pharmacokinetic
parameters of AFQ056 immediate release forms (50 mg AFQ056 capsule
and 400 mg AFQ056 capsule) change dramatically in the presence of
ethanol. Tmax is reached faster and both Cmax and AUC.sub.48h are
higher for an immediate relase form in the presence of ethanol.
Immediate release forms of AFQ056 have therefore the inherent risk
of dose dumping and can create severe consequences for the patient
if ethanol-containing beverages are consumed in parallel. Particle
size distribution is also an important factor influencing the
dissolution of a drug substance and is known to influence the drug
release from matrix tablets.
[0048] Description of the dynamics of getting AFQ056 into solution
is finally related to various factors such as the intrinsic
properties of AFQ056, the composition of the described dissolution
media, specific properties of HPMC (hypromellose) influencing
solubility/dissolution rate of AFQ056 and the resulting viscosity
in the surrounding of the solids to be dissolved.
[0049] Despite the solubility characteristics of AFQ056 (factor
2500x solubility increase in ethanol compared to water) it was
surprisingly found that the release rate of the modified release
formulations of the present invention is similar or even slower in
ethanol than that in water. FIG. 3 and FIG. 4 illustrate the
release pattern of the present formulations in ethanol containing
solutions. It is speculated that the combination of several factors
such as the presence of hypromellose, the particle size and the
size distribution of the drug substance result in the observed
release pattern of the AFQ056 modified release formulations.
Surprisingly the predicted pharmacokinetic parameters of the
modified release formulation remain almost equal in the presence of
ethanol (FIG. 7). It is therefore shown that the modified release
form is dose dumping resistant in the presence of ethanol.
[0050] AFQ056 may be prepared as described in WO 03/047581, the
contents of which are incorporated by reference. In the modified
release formulations of the present invention, AFQ056 is present as
free base.
[0051] Excipients that may be used in the formulations of the
present invention are standard excipients commonly used for tablet
dosage forms and include but are not limited to fillers, modified
release agents, disintegrants, lubricants, glidants, solvents,
viscosity agents, emulsifiers, binding agents, buffers, bulking
agents, coloring agents, taste-improving agents, flow agents,
fillers, absorbents and water soluble coatings.
[0052] Examples of fillers which may be used in the formulations of
the present invention include but are not limited to lactose
monohydrate, dibasic calcium phosphate, calcium carbonate, sugar
alcohols (e.g. mannitol), microcrystalline cellulose and starch.
Preferably, lactose monohydrate is used as a filler.
[0053] Examples of modified release agents which may be used in the
formulations of the present invention without being resistant to
dose dumping in the presence of ethanol include but are not limited
to hydroxy propyl methylcellulose (HPMC), also known as
hypromellose, (a) hydrophilic carbohydrate macromolecules (acacia,
agar, alginic acid, carboxymethylcellulose, carrageenans, dextrin,
gellan gum, guar gum, hydroxyethyl cellulose, hydroxypropyl
cellulose, hypromellose, maltodextrin, methylcellulose, pectin,
propylene glycol alginate, sodium alginate, starch, tragacanth, and
xanthan gum) and (b) noncarbohydrate hydrophilic macromolecules,
including gelatin, povidone carbomers, polyethylene oxide, and
polyvinyl alcohol. Modified release agents which may be used in
formulations of the present invention that are dose dumping
resistant in the presence of ethanol are preferably, hypromellose
such as hypromellose type 2208 and type 2910 is used. More
preferably, Methocel K100 Premium LV CR, Methocel K4M Premium CR,
Methocel K15M Premium CR, Methocel K100M Premium CR, Methocel E4M
Premium CR, and Methocel E10M Premium CR is used, in sum
characterized by viscosities between about 80 to about 120000 cP
(20.degree. C.).
[0054] Examples of binders which may be used in the formulations of
the present invention include but are not limited to cellulose
derivatives (e.g. hypromellose, hydroxypropylcellulose,
methylcellulose), gelatin, polyvinylpyrrolidone, copovidone,
starch, sucrose and polyethylene glycol. In a preferred embodiment
hypromellose, type 2910, is used.
[0055] Various glidants may be used in the formulations of the
present invention and include e.g. silicon dioxide asprecipitated
silica and as colloidal silica, colloidal silicon dioxide.
Preferably colloidal silicon dioxide e.g., Aerosil.RTM. is
used.
[0056] Various disintegrants may be used in the formulations of the
present invention, including, but not limited to, sodium starch
glycolate, carboxymethylcellulose sodium /croscarmellose Sodium,
crospovidone/ cross-linked polyvinylpyrrolidone, starches,
celluloses and pullulan. Preferably, sodium starch glycolate is
used.
[0057] Examples of lubricants which may be used in the formulations
of the present invention, include but are not limited to magnesium
stearate, calcium stearate, zinc stearate, stearic acid, sodium
benzoate, sodium stearyl fumarate, sodium lauryl sulfate,
hydrogenated vegetable oil, glycerides (glyceryl behenate and
distearate). In a preferred embodiment, magnesium stearate is used
as lubricant.
[0058] Coatings which may be used in the formulations of the
present invention include but are not limited to hypromellose,
hydroxypropyl cellulose, methylcellulose, povidone, polyvinyl
alcohol, Macrogol poly(vinyl alcohol) grafted copolymer and
starches. In a preferred embodiment hypromellose, macrogol
4000/polyethylene glycol 4000, talc, iron oxide (red, yellow,
black), and titanium dioxide is used.
[0059] The modified release formulations of the present invention
may be made by mixing, aqueous granulation, screening, drying,
tablet compression and film-coating steps, all of which are well
known in the art.
[0060] For example, the modified release formulations are made by
mixing AFQ056, filler, binder and disintegrant in a high shear
granulator for approximately 5 minutes. Purified water is added
under mixing and the mixture kneaded in a high shear granulator.
The granulate is then passed through a screen using a screening
mill and dried in a fluid bed dryer.
[0061] After drying, the granulate is mixed with filler, modified
release agent and glidant, followed by consecutive sieving using a
screening mill and mixing in a diffusion mixer (tumble). A
lubricant is sieved and then added to the mixture from the
diffusion mixer. The composition is then formed by final
mixing.
[0062] The resulting granules of the composition may have a
diameter from a few microns to a few hundred microns; e.g.,
diameters of at most about 450 microns, e.g., 20 to 450 microns,
preferably 50-200 .mu.m, most preferably, 100-200 .mu.m.
[0063] A narrow particle size distribution is preferred. For
example, a preferred particle size distribution is x10.ltoreq.50
.mu.m, x50.ltoreq.100-150 .mu.m and x90 .ltoreq.200-450 .mu.m,
i.e., 10% of particles are smaller than 50 .mu.m, 50% of particles
are smaller than 150 .mu.m, and 90% of particles are smaller than
450 .mu.m.
[0064] The blend is then compressed into tablet cores using a
rotary tablet press. A coating mixture in purified water is
dispersed and the tablet cores are film coated in a pan coater with
perforated coating system.
[0065] Preferably, the modified release formulations are made by
mixing AFQ056, lactose monohydrate, hypromellose (type 2208) and
sodium starch glycolate in a high shear granulator for
approximately 5 minutes. Purified water is added under mixing and
the mixture kneaded in a high shear granulator. The granulate is
then passed through a screen using a screening mill and dried in a
fluid bed dyer.
[0066] After drying, the granulate is mixed with hypromellose (type
2208), lactose monohydrate and colloidal silicon dioxide followed
by consecutive sieving using a screening mill and mixing in a
diffusion mixer (tumble). The magnesium stearate is sieved and then
added to the mixture from the diffusion mixer. The composition is
formed by final mixing. The blend is then compressed into tablet
cores using a rotary tablet press. A coating mixture in purified
water is dispersed and the tablet cores are film coated in a pan
coater with perforated coating system.
[0067] The modified release formulations of the present invention
are useful in treating Parkinson's disease (PD) and effective
amounts of such formulations are administered to such patients.
[0068] The phrases "effective amount", "amount effective" or
"amounts effective" describe concentrations or amounts of the drug
substance according to the present invention, which may be used to
produce a favorable change in L-dopa induced motor complications
such as dyskinesias (LIDs). The total daily effective amount(s) can
be administered in divided doses (e.g., multiple capsules or
tablets).
[0069] Preferably, the total daily effective amount is delivered in
a single dosage form (e.g., one tablet), which in total, delivers
an effective amount of AFQ056. Thus, the drug products of the
present invention may be administered multiple times a day, twice a
day (b.i.d.) or once a day (o.d.). A once a day dose is preferable
since it may lead to increased patient compliance.
[0070] In accordance with the present invention, a single dosage
form of the modified release formulation of the present invention
provides AFQ056 in an amount of about 25 mg to about 250 mg.
Preferably, a single dosage form of the modified release
formulation of the present invention provides AFQ056 in an amount
of about 50 to about 200 mg.
[0071] The drug products of the present invention may be used to
treat nervous system disorders mediated in full or in part by
mGluR5. Such disorders include Parkinson's disease L-dopa induced
dyskinesia, Fragile X syndrome (Martin-Bell syndrome), dyskinesia
in Fragile X syndrome, obsessive compulsory disorders, autism,
cystitis, acute, traumatic and chronic degenerative diseases of the
nervous system such as Parkinson's disease, senile dementia,
Alzheimer's disease, Huntington's chorea, amyotrophic lateral
sclerosis and multiple sclerosis, psychiatric diseases such as
schizophrenia and anxiety, depression, pain, itch and drug abuse,
e.g. alcohol and nicotine abuse and cocaine use disorders.
[0072] The drug products of the present invention may be used in
the manufacture of a medicament for the treatment of Parkinson's
disease L-dopa induced dyskinesia, Fragile X syndrome (Martin-Bell
syndrome), dyskinesia in Fragile X syndrome, obsessive compulsory
disorders, autism, cystitis, and for the treatment, prevention or
delay of progression of acute, traumatic and chronic degenerative
processes of the nervous system, such as Parkinson's disease,
senile dementia, Alzheimer's disease, Huntington's chorea,
amyotrophic lateral sclerosis and multiple sclerosis, psychiatric
diseases such as schizophrenia and anxiety, depression, pain, itch
and drug abuse such as alcohol and nicotine abuse and cocaine use
disorders.
[0073] In a preferred embodiment, the drug products of the present
invention are used to treat Parkinson's Disease-Levodopa Induced
Dyskinesia (PD-LID).
[0074] The following examples further illustrate the invention,
which are not meant in any way to limit the scope thereof.
EXAMPLE 1
[0075] The following formulations (tablet core compositions) of
AFQ056 are made:
TABLE-US-00001 TABLE 1 IR-Caps Form A Form B Form C [mg/dose]
[mg/dose] [mg/dose] [mg/dose] AFQ056 100.00 100.00 100.00 99.00
Lactose monohydrate 100.00 22.00 22.00 21.78 Microcrystalline 20.00
-- -- -- Cellulose Sodium Starch 16.25 12.50 12.50 12.375 glycolate
Hypromellose 10.00 42.80 69.50 71.775 Colloidal Silicon 1.25 0.90
1.00 0.99 Dioxide Magnesium stearate 2.50 1.80 2.00 1.98 Total
250.00 180.00 207.00 207.90 IR-Caps Form A Form B Form C [%] [%]
[%] [%] AFQ056 40.00 55.56 48.31 47.62 Hypromellose 4.00 23.78
33.57 34.52 Lactose monohydrate 40.00 12.22 10.63 10.48
Microcrystalline 8.40 -- -- -- Cellulose Sodium Starch 6.50 6.94
6.04 5.95 glycolate Magnesium stearate 1.00 1.00 0.97 0.95
Colloidal Silicon 0.50 0.50 0.48 0.48 Dioxide
[0076] Since previous oral formulations have exhibited an increased
exposure upon concomitant intake of a high-fat meal, the extent of
which has been found to be formulation-dependent, this study is
designed to assess the food-effect (by administration of a high fat
breakfast) on the PK of the modified release forms.
[0077] The effect of a high-fat breakfast on the pharmacokinetics
and relative bioavailability of three prolonged release
formulations of AFQ056 at a single dose of -100 mg (with reference
to the fasted state PK) is assessed. In addition, the tolerability
of three different prolonged release formulations of AFQ056 at a
single dose of 100 mg under fasted and fed conditions is tested
[0078] An open-label, randomized, five periods, seven treatments
cross-over study in healthy subjects is conducted. A total of forty
five (45) subjects are enrolled to obtain data on at least 30
completers. Each subject receives a total of 5 single doses of
AFQ056; three doses under fasted conditions and two doses under fed
conditions.
[0079] The study consists of a screening period (up to 27 days), 5
baseline periods, 4 wash out periods of 7-2 days inclusive. 5
treatment periods followed by a Study Completion Evaluation 5-10
days (inclusive) after the last drug administration.
[0080] Subjects who meet the eligibility criteria at screening are
admitted to baseline evaluations for treatment period 1. Subjects
are admitted to the study site at least 12 hours prior to dosing in
each period for baseline evaluations. All baseline safety
evaluation results must be available prior to dosing. After an
overnight fast, subjects are randomized to one of the treatment
sequence (Table 2).
Treatment 1: AFQ056 100 mg Form-A. fasted
Treatment 2: AFQ056 100 mg Form-A, fed
[0081] Treatment 3: AFQ056 100 mg Form-B. fasted
Treatment 4: AFQ056 100 mg Form-B. fed
[0082] Treatment 5: AFQ056 99 mg Form-C. fasted
Treatment 6: AFQ056 99 mg Form-C, fed
[0083] Treatment 7: AFQ056 50 mg Capsule, fasted
TABLE-US-00002 TABLE 2 Treatment sequenc per Sequence Period 1
Period 2 Period 3 Period 4 Period 5 1 1 2 3 4 7 2 2 3 4 7 1 3 3 4 7
1 2 4 4 7 1 2 3 5 7 1 2 3 4 6 1 2 5 6 7 7 2 5 6 7 1 8 5 6 7 1 2 9 6
7 1 2 5 10 7 1 2 5 6 11 3 4 5 6 7 12 4 5 6 7 3 13 5 6 7 3 4 14 6 7
3 4 5 15 7 3 4 5 6
[0084] Following each single dose of AFQ056, pharmacokinetic
assessments are made up to 72 h post dose. A wash-out period of
7.+-.2 days inclusive separates each treatment period. The washout
period is calculated between dose to dose and baseline of
subsequent period can overlap with the 5.sup.th day after
dosing.
[0085] The total study duration for each subject lasts a minimum of
53 days and a maximum of 70 days from screening to study
completion. Subject are domiciled for approximately 20 days in
total (4 days for each period) for all sequences.
[0086] The study has a 3-Latin, 5-sequences.times.5-period
open-label design that is suitable for comparing the
pharmacokinetics including relative bioavailability of three
modified release formulations of AFQ056. The immediate release
capsule formulation (size O, IR) is used as a reference to enable
comparisons with data obtained in previously completed trials. This
study design allows the comparison of pharmacokinetic profile of
AFQ056 from three modified release (MR) formulations relative to
the IR formulation under fasted conditions, and to assess the food
effect on the pharmacokinetics of the three MR forms. Latin-square
design is selected as it offers maximum precision of comparison
across different treatments with minimum number of study subjects.
The cross-over design permits investigation of all five treatment
conditions within each subject and is used to account for
interindividual variability. A wash out period of at least 5 days
ensures complete washout of AFQ056 based on a half life of 7 to 17
hours for 50 mg and for 100 mg doses. Sampling for 72 hours post
dose is considered sufficient for characterizing the PK profiles of
all formulations, including the MR forms.
[0087] Comparisons of the concentration-time profile for the fasted
and fed conditions for all formulations are provided in FIG. 9.
[0088] Mean (SD) plasma concentration-time profile of selected
modified release formulation form B, fasted versus fed, is depicted
in FIG. 10.
The results of the non-compartmental PK analysis are summarized in
Table 3. For better comparability the PK parameters were normalized
to dose where necessary.
TABLE-US-00003 TABLE 3 Key PK parameters (average +/- SD) from
preliminary analysis for market formulation (MF) IR and
modified-release (MR) formulation AUC0-24 h/ Food Cmax/Dose dose
Ratio State n Tmax.sup.1) [h] [ng/mL] [ng * h/mL] Cmax/AUC MR
Fasted 23 3.0 1.760 13.027 0.137 Formulation A (2.0-6.0) (0.754)
(4.950) (0.33) Fed 23 4.0 3.437 17.612 0.206 (1.5-10.0) (1.777)
(9.919) (0.054) MR Fasted 21 4.0 1.076 12.165 0.092 Formulation B
(1.5-6.0) (0.456) (5.766) (0.023) Fed 21 6.0 2.555 16.070 0.168
(2.0-24.0) (1.067) (7.418) (0.051) MR Fasted 21 3.0/ 0.926 12.828
0.083 Formulation C 2.0-8.0) (0.281) (6.989) (0.036) Fed 22 4.0
2.570 17.595 0.158 (2.0-8.0) (0.868) (7.600) (0.047) IR Capsule
Fasted 33 1.0 2.955 14.071 0.221 (0.5-6.0) (1.340) (6.956) (0.070)
.sup.1)values for Tmax are median (range)
[0089] Results indicate that modified release (MR) forms show a
decrease in Cmax (at Tmax) with very little loss of AUC. Cmax/AUC
ratios are favorable for all modified release forms over the
intermediate release (IR) form with the best ratio for Form B and
C. All MR forms have a positive food effect with increased Cmax
compared to the fasted state.
EXAMPLE 2
[0090] The tablet core is formulated using common excipients for
such pharmaceutical dosage forms. Release of the drug substance
from the tablet core occurs through an erosion and diffusion
mechanism, and is controlled by the hypromellose (type 2208)
content of the formulated product. A pharmacokinetic study is
performed using different 100 mg modified release tablet
formulations in order to evaluate the impact of delaying release of
the active ingredient.
[0091] The same ratio of excipients in the 100 mg tablet core is
used to create the additional dosage strengths. The lower dosage
strengths e.g. 25 mg, 50 mg and 75 mg use lactose monohydrate as
compensation for drug substance in order to maintain the tablet
weight and size. The tablet cores of dosage strengths less than or
equal to 100 mg are compressed to round tablets possessing a
diameter of 8 mm.
[0092] For the higher dosage strengths e.g. 150 mg, 200 mg and 250
mg, the tablet weight and size are increased. The same formulation
principle is applied i.e. using lactose monohydrate as compensation
for drug substance. The tablet cores of dosage strengths more than
100 mg are compressed to round tablets possessing a diameter of 11
mm. Table 4 summarizes the tablet core composition of the different
dosage strengths.
TABLE-US-00004 TABLE 4 Tablet core composition overview for AFQ056
MR FCT Amount per film-coated tablet (mg) Ingredient 25 mg 50 mg
100 mg 150 mg 200 mg 250 mg AFQ056 25.00 50.00 100.00 150.00 200.00
250.00 Lactose 96.30 71.20 22.00 152.00 100.50 55.00 monohydrate
Sodium starch 3.13 6.25 12.50 18.75 25.00 31.25 glycolate
Hypromellose 79.48 76.35 69.5 120.75 115.90 105.25 Magnesium 2.00
2.00 2.00 4.50 4.40 4.50 Stearate Colloidal 1.00 1.00 1.00 2.00
2.20 2.00 silicon dioxide Core tablet 206.9 206.8 207.0 448.0 448.0
448.0 weight
[0093] Dissolution of AFQ056 modified release film-coated tablets
occurs through an erosion and diffusion mechanism, with a target
release time of approximately 6 to 7 hours for >80% of the
active ingredient (Table 5). The dissolution method uses
dissolution apparatus 2 (paddle) at 100 rpm with 900 ml of
Water+0.5% LDAO. Comparative dissolution profiles for AFQ056
modified release film-coated tablets are provided in FIG. 8.
TABLE-US-00005 TABLE 5 Dissolution results for AFQ056 MR
Film-coated tablets Amount of AFQ056 released (%) in:
Strength/Batch No. 60 min 180 min 240 min 360 min 420 min 25
mg/X217 0911 13.9 51.4 67.3 90.1 95.6 50 mg/X218 0911 19.1 59.4
75.9 94.6 98.6 100 mg/X220 0911 16.1 58.2 73.8 95.3 98.6 150
mg/X221 0911 20.4 61.1 76.5 95.2 98.1 200 mg/X266 1111 20.0 57.4
71.5 90.8 95.4
EXAMPLE 3
[0094] Particle size distribution is an important factor in
dissolution of the modified release forms of the present invention.
The following experiments are performed to in order to determine
how particle size effects dissolution at various time points.
[0095] FIG. 11 graphically depicts the percentage of AFQ056
dissolved after 45 minutes versus particle size at x90. As can be
discerned from the figure, particle size distribution is a key
factor in dissolution rate and thus the performance of the MR Form.
The drug substance has a particle size distribution of
x10.ltoreq.50 .mu.m, x50.ltoreq.100 .mu.m and x90.ltoreq.200
.mu.m.
* * * * *