U.S. patent application number 16/509919 was filed with the patent office on 2020-03-19 for prolonged release formulations comprising an 2-oxo-1-pyrrolidine derivative.
The applicant listed for this patent is UCB Biophama SPRL. Invention is credited to Monique Berwaer, Frederic Eeckman, Domenico Fanara.
Application Number | 20200085754 16/509919 |
Document ID | / |
Family ID | 41381618 |
Filed Date | 2020-03-19 |
![](/patent/app/20200085754/US20200085754A1-20200319-C00001.png)
United States Patent
Application |
20200085754 |
Kind Code |
A1 |
Fanara; Domenico ; et
al. |
March 19, 2020 |
Prolonged Release Formulations Comprising an 2-Oxo-1-Pyrrolidine
Derivative
Abstract
The present invention relates to a pharmaceutical composition
comprising Levetiracetam, Brivaracetam or Seletracetam as active
ingredient, the invention relates specifically to a prolonged
release formulation.
Inventors: |
Fanara; Domenico; (Brussels,
BE) ; Eeckman; Frederic; (Brussels, BE) ;
Berwaer; Monique; (Brussels, BE) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
UCB Biophama SPRL |
Brussels |
|
BE |
|
|
Family ID: |
41381618 |
Appl. No.: |
16/509919 |
Filed: |
July 12, 2019 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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16241184 |
Jan 7, 2019 |
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16509919 |
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13129114 |
Jun 24, 2011 |
10172805 |
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PCT/EP2009/065271 |
Nov 17, 2009 |
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16241184 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61K 47/32 20130101;
A61P 25/06 20180101; A61K 31/4015 20130101; A61K 47/38 20130101;
A61P 25/16 20180101; A61K 9/16 20130101; A61K 9/5078 20130101; A61P
25/14 20180101; A61P 25/00 20180101; C07D 207/27 20130101; A61P
25/08 20180101; A61P 29/00 20180101 |
International
Class: |
A61K 9/50 20060101
A61K009/50; C07D 207/27 20060101 C07D207/27; A61K 31/4015 20060101
A61K031/4015; A61K 47/38 20060101 A61K047/38; A61K 47/32 20060101
A61K047/32; A61K 9/16 20060101 A61K009/16 |
Foreign Application Data
Date |
Code |
Application Number |
Nov 18, 2008 |
EP |
08105817.4 |
Jun 2, 2009 |
EP |
09100312.9 |
Claims
1. A pharmaceutical composition comprising a granulate containing
an inert core which is coated by a first layer comprising an active
ingredient and at least one excipient, the first layer being coated
by a controlled release layer, wherein the active ingredient is
Brivaracetam.
2. The pharmaceutical composition according to claim 1, wherein
R.sup.1 is hydrogen, n-propyl or 2,2-diflurorovinyl; R.sup.2 is
ethyl; and X is --CONH.sub.2.
3. The pharmaceutical composition according to claim 1, wherein the
weight percentage of the controlled release layer is between 1.0%
and 60%, relative to the weight of the pharmaceutical
composition.
4. The pharmaceutical composition according to claim 1, wherein the
controlled release layer comprises ammonioalkyl methacrylate ethyl
acrylate copolymers, ethylacrylate methyl methacrylate copolymer,
ethylcellulose, or cellulose acetate having a level of acetyl group
comprised between 32% and 44%, or a combination thereof.
5. The pharmaceutical composition according to claim 4, wherein the
controlled release polymer is a copolymer of ammonioalkyl
methacrylate and ethyl acrylate, having an average molecular weight
comprised between 75000 and 200.000 da, and having a level of
ammonioalkyl methacrylate moieties of between 6% and 14%; or a
copolymer of ethyl acrylate and methyl methacrylate in a molar
ratio of 2:1 of the two monomers and having an average molecular
weight of between 500000 and 1000000.
6. The pharmaceutical composition according to claim 1, wherein the
controlled release layer comprises an excipient.
7. The pharmaceutical composition according to claim 1, wherein the
inert core is a sphere having a sphericity degree greater than 0.75
and having a density of between 0.5 and 1.5.
8. The pharmaceutical composition according to claim 1, wherein the
inert core consists essentially of microcrystalline cellulose.
9. The pharmaceutical composition according to claim 1, wherein the
average particle size of the inert core is between 75 and 1400
.mu.m.
10. The pharmaceutical composition according to claim 1, wherein
the excipients of the first layer comprise
hydroxylpropylmethylcellulose and talc.
11. The pharmaceutical composition according to claim 1, wherein
the granulate is coated with an intermediate layer.
12. The pharmaceutical composition according to claim 1, wherein
the granulate coated with the controlled release layer is further
coated with the final layer.
13. The pharmaceutical composition according to claim 1, wherein an
external phase is added.
14. The pharmaceutical composition according to claim 6, wherein
the excipient is a co-binder, an anti-sticking agent, and antifoam
agent, a flavoring agent, a pigment, a plasticizer, an emulsifier,
or a stabilizer.
15. A pharmaceutical composition comprising a granulate wherein the
granulate comprises (a) an inert core; (b) a first layer coating on
the core, wherein the first layer comprises Brivaracetam and
hydroxypropylmethylcellulose; and (c) a controlled release layer
coating the first layer, wherein the controlled release layer
comprises an acrylate copolymer and
hydroxypropylmethylcellulose.
16. A pharmaceutical composition according to claim 15, wherein the
acrylate copolymer is a copolymer of ethyl acrylate and methyl
methacrylate.
17. A pharmaceutical composition according to claim 15, wherein the
amount of Brivaracetam is about 20% by weight of the combined
weights of the inert core and the first layer.
18. A pharmaceutical composition according to claim 15, wherein the
amount of the acrylate copolymer is about 11% by weight of the
combined weights of the inert core, the first layer, and the
controlled release layer.
Description
[0001] The present invention concerns a pharmaceutical oral
composition of 2-oxo-1-pyrrolodine derivatives, a process of the
preparation thereof and therapeutic uses thereof.
[0002] (S)-(-).alpha.-ethyl-2-oxo-1-pyrrolidineacetamide, is also
known and hereinafter referred to as Levetiracetam. The use of
Levetiracetam, as a protective agent for the treatment and
prevention of hypoxic and ischaemic type aggressions of the central
nervous system (CNS) is described in European patent EP-B-0 162
036. The compound can also be employed in the treatment of
epilepsy, a therapeutic indication for which it has been
demonstrated that its dextrorotatory enantiomer,
(R)-(+)-.alpha.-ethyl-2-oxo-1-pyrrolidine-acetamide, is completely
devoid of activity (A. J. GOWER et al., Eur. J. Pharmacol., 222,
(1992), 193-203).
[0003] International patent application having publication number
WO 01/62726 discloses 2-oxo-1-pyrrolidine derivatives and methods
for their preparation. It particularly discloses compound
(2S)-2-[(4R)-2-oxo-4-propyl-pyrrolidin-1-yl]butanamide known under
the international non propriety name of Brivaracetam.
[0004] International patent application having publication number
WO 2005/121082 describes a process of preparation of
2-oxo-1-pyrrolidine derivatives and particularly discloses a
process of preparation of
(2S)-2-[(4S)-4-(2,2-difluorovinyl)-2-oxo-pyrrolidin-1-yl]butanamide
known under the international non propriety name of Seletracetam.
[0005] 2-oxo-1-pyrrolidine derivatives are therefore particularly
useful in the pharmaceutical industry.
[0006] Brivaracetam is effective in the treatment of epilepsy. A
clinical trial evaluated the efficacy and safety of Brivaracetam
(5, 20 and 50 mg per day) in the adjunctive treatment of adult
patients with refractory partial onset seizures, with or without
secondary generalization. Brivaracetam is also effective in the
treatment of patients with post-herpetic neuralgia.
[0007] Seletracetam is effective in the treatment of epilepsy. Two
studies were conducted with Seletracetam in epilepsy evaluating the
efficacy and safety of Seletracetam in the adjunctive treatment of
partial onset seizures in highly refractory adult patients
currently receiving up to three concomitant anti-epileptic
drugs.
[0008] A prolonged release formulation would be particularly
desirable for administration in some patients. A prolonged release
formulation could be advantageously used in order to reduce the
difference between plasmatic C.sub.max and C.sub.min and
consequently to lower sides effects. Moreover, a prolonged release
formulation improves the patient's compliance as the administration
frequency could be reduced.
[0009] A same formulation which can be easily adapted for various
dosages of active ingredient would be also desirable.
[0010] Moreover, a formulation easily ingested would be
particularly desirable for administration in children and also in
some elderly adult patients.
[0011] A prolonged release formulation once a day, would be
particularly desirable.
[0012] International patent application WO 2006/088864 and US
application US 2007/298098 disclose controlled release compositions
which deliver Levetiracetam in a pulsatile manner, comprising a
first component comprising a first population of Levetiracetam
particles and a second component comprising a subsequent population
of Levetiracetam particles coated with a modified release
coating.
[0013] It has now surprisingly been found that sustained release
behaviour could be obtained from sufficiently small size pellets
and an accurate control of the release could be obtained thanks to
the use of a controlled release coating.
[0014] One of the objectives of the invention is a pharmaceutical
composition which can be administered orally to control the release
of pharmaceutically active substances so that it can be
administered in a few daily doses, ideally in a single daily dose
and so to provide a therapeutic effect for at least 16 hours when
administered to a patient.
[0015] Considering Levetiracetam, Brivaracetam and Seletracetam are
classified as BCS I, in order to achieve a prolonged therapeutic
plasmatic drug level the resulting in vitro dissolution (USP
<711> apparatus no 2) in a buffered aqueous media has to show
a drug release of no more than 40% after 1 hour of dissolution, of
25%-80% after 4 hours of dissolution and of no less than 80% after
16 hours of dissolution. Preferably, a profile of no more than 35%
after 1 hour of dissolution, of 35%-75% after 4 hours of
dissolution and of no less than 80% after 16 hours of dissolution.
More preferably a profile of no more than 30% after 1 hour of
dissolution, of 45%-70% after 4 hours of dissolution and of no less
than 80% after 16 hours of dissolution.
[0016] However, as Levetiracetam, Brivaracetam and Seletracetam
have a very high water solubility (their solubility exceeds 500
mg/ml), it is therefore not obvious to slow down their release to
such an extent, above all when non-monolithic forms are used, as
the total surface area is consequently dramatically increased.
[0017] Accordingly, the present invention relates to a
pharmaceutical composition comprising a granulate containing an
inert core which is coated by a first layer comprising an active
ingredient and at least one excipient, this first layer being
coated by a second layer which is a controlled release layer, and
the active ingredient being an 2-oxo-1-pyrrolidine derivative of
formula (I),
##STR00001##
[0018] wherein,
[0019] R.sup.1 is H, C.sub.1-10 alkyl or C.sub.2-6 alkenyl;
[0020] R.sup.2 is C.sub.1-10 alkyl or C.sub.2-6 alkenyl;
[0021] X is --CONR.sup.4R.sup.5, --COOH, --COOR.sup.3 or --CN;
[0022] R.sup.3 is C.sub.1-10 alkyl;
[0023] R.sup.4 is hydrogen or C.sub.1-10 alkyl;
[0024] R.sup.5 is hydrogen or C.sub.1-10 alkyl.
[0025] The term "active ingredient" as used herein is defined as a
substance or a drug which has a therapeutic effect. It can also be
a mixture of substances having a therapeutic effect.
[0026] The amount of the active ingredient present in the
pharmaceutical composition of the invention may vary depending on
the patient to which the compositions are administered and the
disease to be treated.
[0027] The term "alkyl", as used herein, is a group which
represents saturated, monovalent hydrocarbon radicals having
straight (unbranched), branched or cyclic moieties, or combinations
thereof. Preferred alkyl comprises 1 to 10 carbons. More preferred
alkyl comprises 1 to 4 carbons. Optionally, alkyl groups may be
substituted by 1 to 5 substituents independently selected from the
group consisting of halogen, hydroxy, alkoxy, ester, acyl, cyano,
acyloxy, acid, amide or amino group. Preferred alkyl groups are
methyl, ethyl, n-propyl, trifluoromethyl and trifluoroethyl.
[0028] The term "alkenyl" as used herein represents unsubstituted
or substituted branched, unbranched or cyclic hydrocarbon radicals
or combinations thereof having at least one double bond. Preferred
alkenyl comprises 2 to 6 carbons. More preferred alkenyl comprises
2 to 4 carbons. "Alkenyl" moieties may be optionally substituted by
1 to 5 substituents independently selected from the group
consisting of halogen, hydroxy, alkoxy, ester, acyl, cyano,
acyloxy, carboxylic acid, amide or amino group.
[0029] The term "halogen", as used herein, represents an atom of
fluorine, chlorine, bromine, or iodine.
[0030] The term "hydroxy", as used herein, represents a group of
formula --OH.
[0031] The term "alkoxy", as used herein, represents a group of
formula --OR.sup.a wherein R.sup.a is C.sub.1-4 alkyl as defined
above.
[0032] The term "acyl" as used herein, represents a group of
formula R.sup.bCO--, wherein R.sup.b represents a C.sub.1-4 alkyl
as defined above.
[0033] The term "ester", as used herein, represents a group of
formula --COOR.sup.c wherein R.sup.c represents a C.sub.1-4 alkyl
as defined above.
[0034] The term "cyano" as used herein represents a group of
formula --CN.
[0035] The term "acyloxy" as used herein represents a group of
formula --O--COR.sup.d, wherein R.sup.d is a C.sub.1-4 alkyl as
defined above or an aryl group.
[0036] The term "aryl" as used herein, represents an organic
radical derived from an aromatic hydrocarbon by removal of one
hydrogen, for example a phenyl.
[0037] The term "carboxylic acid" as used herein represents a group
of formula --COOH.
[0038] The term "amino group", as used herein, represents a group
of formula --NH.sub.2, NHR.sup.e or NR.sup.fR.sup.e wherein R.sup.e
and R.sup.f are alkyl groups as defined above in the
specification.
[0039] The term "amide", as used herein, refers to a group of
formula --CO--NH.sub.2, --CO--NHR.sup.g, or --CO--NR.sup.gR.sup.h,
wherein R.sup.g and R.sup.h are alkyl groups as defined above in
the specification.
[0040] The term "sulfonate group" as used herein represents a group
of formula --O--SO.sub.2--R.sup.i wherein R.sup.i is an alkyl or an
aryl as defined here above in the specification.
[0041] Preferred sulfonate groups are methanesulfonate,
para-toluenesulfonate group or trifluoromethanesulfonate.
[0042] Compounds of formula (I) have at least two stereogenic
centers in their structure which are indicated by (1*) and (2*).
These stereogenic centers may be present in a R or S configuration,
said R and S notation being used in accordance with the rules
described in Pure. Appl. Chem., 45 (1976) 11-30.
[0043] In one embodiment, according to first aspect of the present
invention, R.sup.1 is H, C.sub.1-4 alkyl or C.sub.2-4 alkenyl. In a
further embodiment according to first aspect of the present
invention, R.sup.1 is hydrogen, n-propyl or 2,2-difluorovinyl.
[0044] In one embodiment according to first aspect of the present
invention, R.sup.2 is C.sub.1-4 alkyl. In another embodiment
according to first aspect of the present invention, R.sup.2 is
ethyl.
[0045] In one embodiment according to first aspect of the present
invention, X is --CONR.sup.4R.sup.5, --COOH or --COOR.sup.3,
wherein R.sup.3 is a C.sub.1-4 alkyl. In another embodiment
according to first aspect of the present invention, X is
--CONR.sup.4R.sup.5.
[0046] In one embodiment according to first aspect of the present
invention, X is --CONR.sup.4R.sup.5 or --COOR.sup.3, wherein
R.sup.3 is a C.sub.1-4 alkyl. In another embodiment according to
first aspect of the present invention, X is COOR.sup.3, wherein
R.sup.3 is a C.sub.1-4 alkyl.
[0047] In one embodiment according to first aspect of the present
invention, X is --CONR.sup.4R.sup.5 or --COOR.sup.3, wherein
R.sup.3 is a C.sub.1-4 alkyl. In another embodiment according to
first aspect of the present invention, X is COOR.sup.3, wherein
R.sup.3 is a C.sub.1-4 alkyl.
[0048] In a particular embodiment, R.sup.3 is methyl.
[0049] In one embodiment according to first aspect of the present
invention, R.sup.4 is hydrogen or C.sub.1-4 alkyl. In another
embodiment according to first aspect of the present invention,
R.sup.4 is hydrogen.
[0050] In one embodiment according to first aspect of the present
invention, R.sup.5 is hydrogen or C.sub.1-4 alkyl. In another
embodiment according to the first aspect of the present invention,
R.sup.5 is hydrogen.
[0051] Preferably R.sup.1 is hydrogen, n-propyl or
2,2-difluorovinyl; R.sup.2 is ethyl; and X is --CONH.sub.2.
[0052] More preferably, the active ingredient is selected among
Brivaracetam, Seletracetam and Levetiracetam. The best results have
been obtained with Brivaracetam and Seletracetam.
[0053] Accordingly, the present invention relates to a
pharmaceutical composition comprising a granulate which contains an
active ingredient and which is coated with a controlled release
layer. Usually, the weight percentage of the controlled release
layer is comprised between 1.0% and 60%, relative to the weight of
the pharmaceutical composition. Preferably, the weight percentage
of the controlled release layer is comprised between 2.0% and 50%.
More preferably, the weight percentage of the controlled release
layer is comprised between 5.0% and 40%, relative to the weight of
the pharmaceutical composition.
[0054] According to the invention, the controlled release layer
comprises at least a controlled release polymer. By controlled
release polymer, it is understood a polymer that could control the
release rate of the active ingredient thanks to its
solubility/permeability properties in an aqueous environment.
[0055] Generally, the controlled release polymer consists in
ammonioalkyl methacrylate ethyl acrylate copolymers, or in
ethylacrylate methyl methacrylate copolymer, or in ethylcellulose,
or in cellulose acetate having a level of acetyl group comprised
between 32% and 44%, or in a mix of thereof. Preferably, the
controlled release polymer is chosen among a copolymer of
ammonioalkyl methacrylate and ethyl acrylate, having an average
molecular weight comprised between 75000 and 200.000 da, and having
a level of ammonioalkyl methacrylate moieties comprised between 6%
and 14%; or a copolymer of ethyl acrylate and methyl methacrylate
in a molar ratio of 2:1 of the two monomers and having an average
molecular weight comprised between 500000 and 1000000. Best results
have been obtained with a copolymer of ammonioalkyl methacrylate
and ethyl acrylate, sold under the trade name Eudragit.RTM. RS or
Eudragit.RTM. RL and marketed by Evonik Industries AG; and with a
copolymer of ethyl acrylate and methyl methacrylate sold under the
trade name Eudragit.RTM. NE 30 D and marketed by Evonik Industries
AG, as a 30% aqueous dispersion.
[0056] Usually, the controlled release layer contains at least an
excipient, such as co-binders, antisticking agents, antifoams,
flavoring agents, pigment, processing aid agents, like
plasticizers, emulsifier or stabilizer.
[0057] Generally the controlled release layer comprises a
co-binder. Generally, the co-binder is chosen among cellulose
derivatives, polyvinylalcohol or polyvinylpyrrolidone or a mixture
thereof. Preferably, the co-binder is a cellulose derivative. More
preferably it is hydroxypropylmethylcellulose (HPMC). The best
results have been obtained with hydroxypropylmethylcellulose USP 28
designation type 2910 as co-binder.
[0058] Generally the controlled release layer comprises an
antisticking agent. Generally, the antisticking agent is chosen
among talc, colloidal silicon dioxide, magnesium trisilicate,
starch, tribasic calcium phosphate, or a mixture thereof.
Preferably, it is talc.
[0059] Usually, the pharmaceutical composition according to the
present invention comprises 30 to 100% per weight of controlled
release polymer with respect to the total dry mass of the
controlled release layer. Preferably, the pharmaceutical
composition according to the present invention comprises 40 to 90%
per weight of controlled release polymer, more preferably 60 to 75%
per weight of controlled release polymer with respect to the total
dry mass of the controlled release layer.
[0060] Usually, the pharmaceutical composition according to the
present invention comprises 0 to 15% per weight of co-binder with
respect to the total dry mass of the controlled release layer.
Preferably, the pharmaceutical composition according to the present
invention comprises 1 to 10% per weight of co-binder, more
preferably 3 to 5% per weight of co-binder with respect to the
total dry mass of the controlled release layer.
[0061] Usually, the pharmaceutical composition according to the
present invention comprises 0 to 50% per weight of the antisticking
agent with respect to the total dry mass of the controlled release
layer. Preferably, the pharmaceutical composition according to the
present invention comprises 10 to 45% per weight of the
antisticking agent, more preferably 25 to 35% per weight of the
antisticking agent with respect to the dry mass of the controlled
release layer.
[0062] Generally, the inert core is a sphere having a sphericity
degree greater than 0.75 and having a density comprised between 0.5
and 1.5. Preferably, the inert core is a sphere having a sphericity
degree comprised greater than 0.85 and having a density comprised
between 0.6 and 1.2 Best results have been obtained with a sphere
having a sphericity degree greater than 0.90, and having a density
comprised between 0.80 and 0.90. By sphericity degree, it is
understood the ratio of the surface area of a sphere (having the
same volume as the given particle) to the surface area of the
particle.
[0063] Generally, the inert core is neutral (i.e. it does not
contain any active material).
[0064] Usually, the inert core is composed by sugar, saccharides,
polysaccharides, cellulose, cellulose derivatives, microcrystalline
cellulose, starch and/or waxes. Preferably the inert core comprises
microcrystalline cellulose. More preferably, the inert core
consists essentially in microcrystalline cellulose.
[0065] Generally, the average particle size of the inert core is
between 75 and 1400 .mu.m. Preferably, the average particle size of
the inert core is between 400 and 1100 .mu.m. More preferably, the
average particle size of the inert core is between 500 and 1000
.mu.m. The best results have been obtained with neutral spheres of
microcrystalline cellulose, sugar free, sold by Pharmatrans Sanaq
AG under the trademark Cellets.RTM. or sold by Asahi Kasei, under
the trade name Celphere.RTM.; and, in particular, Cellets.RTM. 500,
having an average particle size of 500-710 .mu.m, Cellets.RTM. 700,
having an average particle size of 700-1000 .mu.m, Celphere.RTM.
CP-507 having an average particle size of 500-710 .mu.m and
Celphere.RTM. CP-708 having an average particle size of 710-850
.mu.m.
[0066] According to the invention, the first layer comprises an
active ingredient and at least one excipient. Depending on the
final dose, the level of the active layer could be varied.
[0067] Usually, the weight percentage of the first layer is
comprised between 0.25% and 150%, relative to the weight of the
inert core.
[0068] Preferably, the weight percentage of the first layer is
comprised between 0.5% and 120%, relative to the weight of the
inert core.
[0069] More preferably, the weight percentage of the first layer is
comprised between 1.0% and 100%, relative to the weight of the
inert core.
[0070] Usually, the excipient of the first layer comprises a
binder.
[0071] Generally, the binder is chosen among cellulose derivatives,
polyvinylalcohol, polyvinylpyrrolidone or a mixture thereof.
Preferably, the binder is a cellulose derivative. More preferably,
the binder is hydroxypropylmethylcellulose (HPMC). The best results
have been obtained with hydroxypropylmethylcellulose USP 28
designation type 2910.
[0072] Usually, the excipient of the first layer comprises an
antisticking agent. Generally, the antisticking agent is chosen
among talc, colloidal silicon dioxide, magnesium trisilicate,
starch, tribasic calcium phosphate, or a mixture thereof.
Preferably, the antisticking agent is talc.
[0073] Preferably, the excipients of the first layer comprise
hydroxylpropylmethyl-cellulose and talc.
[0074] Optionally, the excipient of the first layer comprises a
preservative agent. Generally, the preservative agent is chosen
among disodium edetate, sodium metabisulfite, ascorbic acid,
butylated hydroxytoluene, citric acid or a mixture thereof.
Preferably, the preservative agent is disodium edetate.
[0075] Usually, the pharmaceutical composition according to the
present invention comprises 1 to 35% per weight of binder with
respect to the total weight of the dry mass of the first layer.
Preferably, the pharmaceutical composition according to the present
invention comprises 2 to 25% per weight of binder, more preferably
5 to 15% per weight of binder with respect to the dry mass of the
first layer.
[0076] Usually, the pharmaceutical composition according to the
present invention comprises 0 to 40% per weight of the antisticking
agent with respect to the dry mass of the first layer. Preferably,
the pharmaceutical composition according to the present invention
comprises 5 to 35% per weight of the antisticking agent, more
preferably 10 to 30% per weight of the antisticking agent with
respect to the dry mass of the first layer.
[0077] Usually, the pharmaceutical composition according to the
present invention comprises 0 to 5% per weight of the preservative
agent with respect to the dry mass of the first layer. Preferably,
the pharmaceutical composition according to the present invention
comprises 0 to 3% per weight of the preservative agent, more
preferably 0 to 2% per weight of the preservative agent with
respect to the dry mass of the first layer.
[0078] In another embodiment of the invention, an intermediate
layer is added before the controlled release layer, in order to
prevent any diffusion of the active ingredient into the controlled
release layer, or to better protect the active ingredient against
external chemical aggression. The granulate is coated with the
intermediate layer. Generally, the intermediate layer comprises a
binder, an anti-sticking agent, pigments, and/or processing aid
agents like plasticizers.
[0079] Usually, the weight percentage of the intermediate layer is
comprised between 1.0% and 30%, relative to the total weight of the
inert core and the first layer.
[0080] Preferably, the weight percentage of the intermediate layer
is comprised between 2.5% and 20%, relative to the total weight of
the core and the first layer. More preferably, the weight
percentage of the intermediate layer is comprised between 5% and
15%, relative to the total weight of the core and the first
layer.
[0081] Usually, the intermediate coating layer comprises a binder.
Generally, the binder is chosen among cellulose derivatives,
polyvinylalcohol, polyvinylpyrrolidone, or a mixture therefore.
Preferably, the binder is a cellulose derivative. More preferably
it is hydroxypropylmethylcellulose (HPMC). The best results have
been obtained with hydroxypropylmethylcellulose USP 28 designation
type 2910.
[0082] Usually, the intermediate layer comprises an antisticking
agent. Generally, the antisticking agent is chosen among talc,
colloidal silicon dioxide, magnesium trisilicate, starch, tribasic
calcium phosphate, or a mixture thereof. Preferably, it is
talc.
[0083] Optionally, the intermediate layer comprises a plasticizer.
Generally, the plasticizer is chosen among glycerol, fatty acids,
phthalate, low molecular weight polyethylene glycol, citrate or a
mixture thereof. Preferably it is polyethylene glycol.
[0084] By low molecular weight polyethylene glycol, it is
understood polymer having a molecular weight lower than 12000
da.
[0085] Usually, the pharmaceutical composition according to the
present invention comprises 30 to 95% per weight of binder with
respect to the dry mass of the intermediate layer. Preferably, the
pharmaceutical composition according to the present invention
comprises 40 to 90% per weight of binder, more preferably 60 to 80%
per weight of binder with respect to the dry mass of the
intermediate layer.
[0086] Usually, the pharmaceutical composition according to the
present invention comprises 0 to 40% per weight of the
anti-sticking agent with respect to the dry mass of the
intermediate layer. Preferably, the pharmaceutical composition
according to the present invention comprises 5 to 35% per weight of
the anti-sticking agent, more preferably 15 to 25% per weight of
the anti-sticking agent with respect to the dry mass of the
intermediate layer.
[0087] Usually, the pharmaceutical composition according to the
present invention comprises 0 to 25% per weight of plasticizer with
respect to the dry mass of the intermediate layer. Preferably, the
pharmaceutical composition according to the present invention
comprises 2 to 20% per weight of plasticizer, more preferably 6 to
10% per weight of plasticizer with respect to the dry mass of the
intermediate layer.
[0088] In another embodiment of the invention, a final layer is
added after the controlled release layer. The granulate coated with
the controlled release layer is further coated with the final
layer. The final layer comprises a binder, an antisticking agent,
pigments, and/or processing aid agents.
[0089] Usually, the weight percentage of the final layer is
comprised between 1.0% and 30%, relative to the total weight of the
pharmaceutical composition. Preferably, the weight percentage of
the final layer is comprised between 2.5% and 20%. More preferably,
the weight percentage of the final layer is comprised between 5%
and 15%, relative to the total weight of the pharmaceutical
composition.
[0090] In another embodiment of the invention, an external phase is
added. Several pharmaceutically acceptable excipients may be added
to the composition, as external phase ingredient, such as pigment,
preservatives or processing aid agents.
[0091] Examples of processing aid agents are talc, starches,
stearic acid and anhydrous colloidal silica. Preferred processing
aid agent according to the present invention is anhydrous colloidal
silica, such as AEROSIL 200.RTM..
[0092] Usually, the pharmaceutical composition according to the
present invention comprises 0.0 to 3.0% per weight of processing
aid agent. Preferably, the pharmaceutical composition according to
the present invention comprises 0.0 to 2.0% per weight of
processing aid agent, more preferably 0.25 to 1.0% per weight of
processing aid agent with respect to the total weight of the
composition.
[0093] According to the invention, optionally the composition also
contains sweeteners, flavours, palatability agents.
[0094] In one embodiment of the invention, the pharmaceutical
composition comprises
a neutral core having an average particle size between 75 .mu.m and
1400 .mu.m; a first layer with a weight percentage, relative to the
neutral core, between 0.25% and 150%, and containing Brivaracetam,
as active ingredient, and 1 to 35% of binder, 0 to 40% of
anti-sticking agent with respect to the total weight of the first
layer; a controlled release layer with a weight percentage,
relative to the total weight of the pharmaceutical composition,
between 1.0 and 60%, and containing 30 to 100% of controlled
release copolymer, 1 to 15% of binder, 0 to 50% of anti-sticking
agent, respective to the total weight of the controlled release
layer; and an external phase containing a processing aid agent at
level of 0.0 to 3.0% respective to the total weight of the
pharmaceutical composition.
[0095] Particularly, the present invention relates to a
pharmaceutical composition comprising
a neutral core having an average particle size between 400 .mu.m
and 1100 .mu.m; a first layer with a weight percentage, relative to
the neutral core, between 0.5% and 120%, and containing
Brivaracetam, as active ingredient, and 2 to 25% of binder, 5 to
35% of antisticking agent with respect to the total weight of the
first coating layer; a controlled release layer with a weight
percentage, relative to the total weight of the pharmaceutical
composition between 2.0 and 50%, and containing 40 to 90% of
controlled release copolymer, 1 to 10% of binder, 10 to 45% of
antisticking agent, respective to the total weight of the
controlled release layer; and an external phase containing a
processing aid agent at level of 0.0 to 2.0% respective to the
total weight of the composition.
[0096] More particularly the present invention relates to a
pharmaceutical composition comprising
a neutral core having an average particle size between 500 .mu.m
and 1000 .mu.m; a first layer with a weight percentage, relative to
the neutral core, between 1.0% and 100%, and containing
Brivaracetam, as active ingredient, and 5 to 15% of binder, 10 to
30% of antisticking agent, with respect to the total weight of the
first coating layer; a controlled release layer with a weight
percentage, relative to the total weight of the pharmaceutical
composition, between 5.0 and 40%, and containing 60 to 75% of
controlled release copolymer, 3 to 5% of binder, 25 to 35% of
antisticking agent, respective to the total weight of the
controlled release layer; and an external phase containing a
processing aid agent at level of 0.25 to 1.0% respective to the
total weight of the composition.
[0097] In a particular embodiment, the present invention relates to
a pharmaceutical composition comprising
a neutral microcrystalline core having an average particle size
between 75 .mu.m and 1400 .mu.m; a first layer with a weight
percentage, relative to the neutral core, between 0.25% and 150%,
and containing Brivaracetam, as active ingredient, and 1 to 35% of
hydroxyl-propylmethylcellulose, 0 to 40% of talc with respect to
the total weight of the first coating layer; a controlled release
layer with a weight percentage, relative to the total weight of the
pharmaceutical composition, between 1.0 and 60%, and containing 30
to 100% of ethylacrylate-methylmethacrylate copolymer, 1 to 15% of
hydroxypropylmethyl-cellulose, 0 to 50% of talc, respective to the
total weight of the controlled release layer; and an external phase
containing colloidal anhydrous silica at level of 0.0 to 3.0%
respective to the total weight of the composition.
[0098] In a particular embodiment, the present invention relates to
a pharmaceutical composition comprising
a neutral microcrystalline core having an average particle size
between 400 .mu.m and 1100 .mu.m; a first layer with a weight
percentage, relative to the neutral core, between 0.5% and 120%,
and containing Brivaracetam as active ingredient and 2 to 25% of
hydroxyl-propylmethylcellulose, 5 to 35% of talc with respect to
the total weight of the first coating layer; a controlled release
layer with a weight percentage, relative to the total weight of the
pharmaceutical composition, between 2.0 and 50%, and containing 40
to 90% of ethylacrylate-methylmethacrylate copolymer, 1 to 10% of
hydroxypropylmethyl-cellulose, and 10 to 45% of talc respective to
the total weight of the controlled release layer and an external
phase containing colloidal anhydrous silica at level of 0.0 to 2.0%
respective to the total weight of the composition.
[0099] More particularly the present invention relates to a
pharmaceutical composition comprising
a neutral core having an average particle size between 500 .mu.m
and 1000 .mu.m; a first layer with a weight percentage, relative to
the neutral core, between 1.0% and 100%, and containing
Brivaracetam as active ingredient and 5 to 15% of
hydroxyl-propylmethylcellulose, 10 to 30% of talc, with respect to
the total weight of the first coating layer; a controlled release
layer with a weight percentage, relative to the total weight of the
pharmaceutical composition, between 5.0 and 40%, and containing 60
to 75% of ethylacrylate-methylmethacrylate copolymer, 3 to 5% of
hydroxypropylmethyl-cellulose, 25 to 35% of talc, respective to the
total weight of the controlled release layer; and an external phase
containing colloidal anhydrous silica at level of 0.25 to 1.0%
respective to the total weight of the composition.
[0100] In another embodiment of the invention, the pharmaceutical
composition comprises
a neutral core having an average particle size between 75 .mu.m and
1400 .mu.m; a first layer with a weight percentage, relative to the
neutral core, between 0.25% and 150%, and containing Seletracetam
as active ingredient and 1 to 35% of binder, 0 to 40% of
antisticking agent with respect to the total weight of the first
coating layer; an intermediate layer with a weight percentage,
relative to the total weight of the neutral core and of the first
layer, between 1% and 30%, and containing 30 to 95% of binder, 0 to
40% of antisticking agent, 0 to 25% of plasticizer with respect to
the total weight of the intermediate coating layer; a controlled
release layer with a weight percentage, relative to the total
weight of the pharmaceutical composition, between 1.0 and 60%, and
containing 30 to 100% of controlled release copolymer, 1 to 15% of
binder, 0 to 50% of antisticking agent respective to the total
weight of the controlled release layer; and an external phase
containing a processing aid agent at level of 0.0 to 3.0%
respective to the total weight of the composition.
[0101] Particularly, the present invention relates to a
pharmaceutical composition comprising
a neutral core having an average particle size between 400 .mu.m
and 1100 .mu.m; a first layer with a weight percentage, relative to
the neutral core, between 0.5% and 120%, and containing
Seletracetam, as active ingredient, and 2 to 25% of binder, 5 to
35% of antisticking agent with respect to the total weight of the
first coating layer; an intermediate layer with a weight
percentage, relative to the total weight of the neutral core and of
the first layer, between 2.5% and 20%, and containing 40 to 90% of
binder, 5 to 35% of antisticking agent, 2 to 20% of plasticizer
with respect to the total weight of the intermediate coating layer;
a controlled release layer with a weight percentage, relative to
the total weight of the pharmaceutical composition, between 2.0 and
50%, and containing 40 to 90% of controlled release copolymer, 1 to
10% of binder, and 10 to 45% of antisticking agent, respective to
the total weight of the controlled release layer; and an external
phase containing a processing aid agent at level of 0.0 to 2.0%
respective to the total weight of the composition.
[0102] More particularly the present invention relates to a
pharmaceutical composition comprising
a neutral core having an average particle size between 500 .mu.m
and 1000 .mu.m; a first layer with a weight percentage, relative to
the neutral core, between 1.0% and 100%, and containing
Seletracetam, as active ingredient, and 5 to 15% of binder, 10 to
30% of antisticking agent with respect to the total weight of the
first coating layer; an intermediate layer with a weight
percentage, relative to the total weight of the neutral core and of
the first layer, between 5% and 15%, and containing 60 to 80% of
binder, 15 to 25% of antisticking agent, 6 to 10% of plasticizer
with respect to the total weight of the intermediate coating layer;
a controlled release layer with a weight percentage, relative to
the total weight of the pharmaceutical composition, between 5.0 and
40%, and containing 60 to 75% of controlled release copolymer, 3 to
5% of binder, 25 to 35% of antisticking agent, respective to the
total weight of the controlled release layer; and an external phase
containing a processing aid agent at level of 0.25 to 1.0%
respective to the total weight of the composition.
[0103] In a particular embodiment, the present invention relates to
a pharmaceutical composition comprising
a neutral microcrystalline core having an average particle size
between 75 .mu.m and 1400 .mu.m; a first layer with a weight
percentage, relative to the neutral core, between 0.25% and 150%,
and containing Seletracetam as active ingredient and 1 to 35% of
hydroxyl-propylmethylcellulose, 0 to 40% of talc with respect to
the total weight of the first coating layer; an intermediate layer
with a weight percentage, relative to the total weight of the
neutral core and of the first layer, between 1.0% and 30%, and
containing 30 to 95% of hydroxypropylmethylcellulose, 0 to 40% of
talc, 0 to 25% of polyethylene glycol with respect to the total
weight of the intermediate coating layer; a controlled release
layer with a weight percentage, relative to the total weight of the
pharmaceutical composition, between 1.0 and 60%, and containing 30
to 100% of ethylacrylate-methylmethacrylate copolymer, 1 to 15% of
hydroxypropylmethylcellulose, 0 to 50% of talc relative to the
total weight of the controlled release layer, and colloidal
anhydrous silica in the external phase at level of 0.0 to 3.0%
respective to the total weight of the composition.
[0104] Particularly, the present invention relates to a
pharmaceutical composition comprising
a neutral microcrystalline core having an average particle size
between 400 .mu.m and 1100 .mu.m; a first layer with a weight
percentage, relative to the neutral core, between 0.5% and 120%,
and containing Seletracetam as active ingredient and 2 to 25% of
hydroxypropylmethylcellulose, 5 to 35% of talc with respect to the
total weight of the first coating layer; an intermediate layer with
a weight percentage, relative to the total weight of the neutral
core and of the first layer, between 2.5% and 20%, and containing
40 to 90% of hydroxypropylmethylcellulose, 5 to 35% of talc, 2 to
20% of polyethylene glycol with respect to the total weight of the
intermediate coating layer; a controlled release layer with a
weight percentage, relative to the total weight of the
pharmaceutical composition, between 2.0 and 50%, and containing 40
to 90% of ethylacrylate-methylmethacrylate copolymer, 1 to 10% of
hydroxypropylmethylcellulose, 10 to 45% of talc, respective to the
total weight of the controlled release layer; and an external phase
containing colloidal anhydrous silica at level of 0.0 to 2.0%
respective to the total weight of the composition.
[0105] More particularly the present invention relates to a
pharmaceutical composition comprising
a neutral core having an average particle size between 500 .mu.m
and 1000 .mu.m; a first layer with a weight percentage, relative to
the neutral core, between 1.0% and 100%, and containing
Seletracetam as active ingredient and 5 to 15% of
hydroxypropylmethylcellulose, 10 to 30% of talc with respect to the
total weight of the first coating layer; an intermediate layer with
a weight percentage, relative to the total weight of the neutral
core and of the first layer, between 5% and 15%, and containing 60
to 80% of hydroxypropylmethylcellulose, 15 to 25% of talc, 6 to 10%
of polyethylene glycol with respect to the total weight of the
intermediate coating layer; a controlled release layer with a
weight percentage, relative to the total weight of the
pharmaceutical composition, between 5.0 and 40%, and containing 60
to 75% of ethylacrylate-methylmethacrylate copolymer, 3 to 5% of
hydroxypropylmethyl-cellulose, 25 to 35% of talc, respective to the
total weight of the controlled release layer; and an external phase
containing colloidal anhydrous silica at level of 0.25 to 1.0%
respective to the total weight of the composition.
[0106] In another embodiment of the invention, the pharmaceutical
composition comprises
a neutral core having an average particle size between 75 .mu.m and
1400 .mu.m; a first layer with a weight percentage, relative to the
neutral core, between 0.25% and 150%, and containing Levetiracetam,
as active ingredient, and 1 to 35% of binder, 0 to 40% of
anti-sticking agent with respect to the total weight of the first
layer; a controlled release layer with a weight percentage,
relative to the total weight of the pharmaceutical composition,
between 1.0 and 60%, and containing 30 to 100% of controlled
release copolymer, 1 to 15% of binder, 0 to 50% of anti-sticking
agent, respective to the total weight of the controlled release
layer; and an external phase containing a processing aid agent at
level of 0.0 to 3.0% respective to the total weight of the
pharmaceutical composition.
[0107] Particularly, the present invention relates to a
pharmaceutical composition comprising
a neutral core having an average particle size between 400 .mu.m
and 1100 .mu.m; a first layer with a weight percentage, relative to
the neutral core, between 0.5% and 120%, and containing
Levetiracetam, as active ingredient, and 2 to 25% of binder, 5 to
35% of antisticking agent with respect to the total weight of the
first coating layer; a controlled release layer with a weight
percentage, relative to the total weight of the pharmaceutical
composition between 2.0 and 50%, and containing 40 to 90% of
controlled release copolymer, 1 to 10% of binder, 10 to 45% of
antisticking agent, respective to the total weight of the
controlled release layer; and an external phase containing a
processing aid agent at level of 0.0 to 2.0% respective to the
total weight of the composition.
[0108] More particularly the present invention relates to a
pharmaceutical composition comprising
a neutral core having an average particle size between 500 .mu.m
and 1000 .mu.m; a first layer with a weight percentage, relative to
the neutral core, between 1.0% and 100%, and containing
Levetiracetam, as active ingredient, and 5 to 15% of binder, 10 to
30% of antisticking agent, with respect to the total weight of the
first coating layer; a controlled release layer with a weight
percentage, relative to the total weight of the pharmaceutical
composition, between 5.0 and 40%, and containing 60 to 75% of
controlled release copolymer, 3 to 5% of binder, 25 to 35% of
antisticking agent, respective to the total weight of the
controlled release layer; and an external phase containing a
processing aid agent at level of 0.25 to 1.0% respective to the
total weight of the composition.
[0109] In a particular embodiment, the present invention relates to
a pharmaceutical composition comprising
a neutral microcrystalline core having an average particle size
between 75 .mu.m and 1400 .mu.m; a first layer with a weight
percentage, relative to the neutral core, between 0.25% and 150%,
and containing Levetiracetam, as active ingredient, and 1 to 35% of
hydroxyl-propylmethylcellulose, 0 to 40% of talc with respect to
the total weight of the first coating layer; a controlled release
layer with a weight percentage, relative to the total weight of the
pharmaceutical composition, between 1.0 and 60%, and containing 30
to 100% of ethylacrylate-methylmethacrylate copolymer, 1 to 15% of
hydroxypropylmethyl-cellulose, 0 to 50% of talc, respective to the
total weight of the controlled release layer; and an external phase
containing colloidal anhydrous silica at level of 0.0 to 3.0%
respective to the total weight of the composition.
[0110] In a particular embodiment, the present invention relates to
a pharmaceutical composition comprising
a neutral microcrystalline core having an average particle size
between 400 .mu.m and 1100 .mu.m; a first layer with a weight
percentage, relative to the neutral core, between 0.5% and 120%,
and containing Levetiracetam as active ingredient and 2 to 25% of
hydroxyl-propylmethylcellulose, 5 to 35% of talc with respect to
the total weight of the first coating layer; a controlled release
layer with a weight percentage, relative to the total weight of the
pharmaceutical composition, between 2.0 and 50%, and containing 40
to 90% of ethylacrylate-methylmethacrylate copolymer, 1 to 10% of
hydroxypropylmethyl-cellulose, and 10 to 45% of talc respective to
the total weight of the controlled release layer and an external
phase containing colloidal anhydrous silica at level of 0.0 to 2.0%
respective to the total weight of the composition.
[0111] More particularly the present invention relates to a
pharmaceutical composition comprising
a neutral core having an average particle size between 500 .mu.m
and 1000 .mu.m; a first layer with a weight percentage, relative to
the neutral core, between 1.0% and 100%, and containing
Levetiracetam as active ingredient and 5 to 15% of
hydroxyl-propylmethylcellulose, 10 to 30% of talc, with respect to
the total weight of the first coating layer; a controlled release
layer with a weight percentage, relative to the total weight of the
pharmaceutical composition, between 5.0 and 40%, and containing 60
to 75% of ethylacrylate-methylmethacrylate copolymer, 3 to 5% of
hydroxypropylmethyl-cellulose, 25 to 35% of talc, respective to the
total weight of the controlled release layer; and an external phase
containing colloidal anhydrous silica at level of 0.25 to 1.0%
respective to the total weight of the composition.
[0112] The pharmaceutical composition of the invention can be
manufactured by any process according to conventional methods known
to the man skilled in the art, such as compression, extrusion, wet
or dry granulation, by binding of powders, by means of spray
processes, rotor granulation or fluidized bed granulation.
[0113] Optionally, the controlled release layer could require to be
cured at a temperature comprised between 20.degree. C. and
75.degree. C., for a duration comprised between 1 h and 5 days.
Preferably, the controlled release layer could require to be cured
at a temperature comprised between 30.degree. C. and 70.degree. C.,
for a duration comprised between 2 h and 3 days. More preferably,
the controlled release layer could require to be cured at a
temperature comprised between 40.degree. C. and 65.degree. C., for
a duration comprised between 8 h and 1 day.
[0114] In a further particular embodiment, the present invention
relates to a pharmaceutical composition comprising 0.20 to 70% per
weight of Brivaracetam, with respect to the total weight of the
composition.
[0115] Usually, in this further particular embodiment, the present
invention relates to a pharmaceutical composition comprising 0.40
to 60% per weight of Brivaracetam with respect to the total weight
of the composition.
[0116] Particularly, in this further particular embodiment, the
present invention relates to a pharmaceutical composition
comprising 0.60 to 50% per weight of Brivaracetam with respect to
the total weight of the composition.
[0117] The pharmaceutical composition according to the present
invention is preferably administered orally.
[0118] The pharmaceutical composition according to the present
invention is preferably administered in the form of a capsule, a
sachet or a tablet.
[0119] Optionally, the pharmaceutical composition according to the
present invention may contain an external diluent or a processing
aid, such as (but not limited to) starch, lactose, microcrystalline
cellulose, talc.
[0120] Optionally, the pharmaceutical composition according to the
present invention may contain a sweetening agent such as sucrose or
saccharine, a coloring agent or a flavoring agent.
[0121] Optionally, the pharmaceutical composition according to the
present invention may comprise a taste-masking agent. In another
further particular embodiment, the present invention relates to a
pharmaceutical composition comprising 0.20 to 70% per weight of
Seletracetam, with respect to the total weight of the
composition.
[0122] Usually, in this further particular embodiment, the present
invention relates to a pharmaceutical composition comprising 0.40
to 60% per weight of Seletracetam with respect to the total weight
of the composition.
[0123] Particularly, in this further particular embodiment, the
present invention relates to a pharmaceutical composition
comprising 0.60 to 50% per weight of Seletrecetam with respect to
the total weight of the composition.
[0124] The pharmaceutical composition according to the present
invention is preferably administered orally.
[0125] The pharmaceutical composition according to the present
invention is preferably administered in the form of a capsule, a
sachet or a tablet Optionally, the pharmaceutical composition
according to the present invention contains an external diluent or
a processing aid, such as (but not limited to) starch, lactose,
microcrystalline cellulose, talc.
[0126] Optionally, the pharmaceutical composition according to the
present invention contains a sweetening agent such as sucrose or
saccharine, a coloring agent or a flavoring agent.
[0127] Optionally, the pharmaceutical composition according to the
present invention comprises a taste-masking agent.
[0128] The present invention also concerns a use of a
pharmaceutical composition for the treatment of disease.
[0129] In another aspect the present invention relates to a
pharmaceutical composition comprising an active ingredient useful
for the treatment or prevention of a disease.
[0130] By the term "disease", we understand a disease selected from
the group consisting of epileptogenesis, seizure disorders,
convulsions, Parkinson's disease, dyskinesia induced by dopamine
replacement therapy, tardive dyskinesia induced by administration
of neuroleptic drugs, Huntington Chorea, and other neurological
disorders including bipolar disorders, mania, depression, anxiety,
attention deficit hyperactivity disorder (ADHD), migraine,
trigeminal and other neuralgia, chronic pain, neuropathic pain,
cerebral ischemia, cardiac arrhythmia, myotonia, cocaine abuse,
stroke, myoclonus, tremor, essential tremor, simple or complex
tics, Tourette syndrome, restless leg syndrome and other movement
disorders, neonatal cerebral haemorrhage, amyotrophic lateral
sclerosis, spasticity and degenerative diseases.
[0131] The term "treatment" as used herein, includes curative
treatment and prophylactic treatment.
[0132] By "curative" is meant efficacy in treating a current
symptomatic episode of a disorder or condition.
[0133] By "prophylactic" is meant prevention of the occurrence or
recurrence of a disorder or condition.
[0134] The present invention concerns also a method for treatment
of a human patient by using the pharmaceutical composition.
[0135] The present invention concerns also the pharmaceutical
composition for use as a medicament for curing the said
disease.
[0136] The present invention concerns also the use of the
pharmaceutical composition for the manufacture of a medicament for
a therapeutic application in the said disease.
[0137] Preferably said disease is selected from the group
consisting essentially of epilepsy, Parkinson's disease,
dyskinesia, migraine, tremor, essential tremor, bipolar disorders,
chronic pain, neuropathic pain. More preferably said disease is
epilepsy.
[0138] The present invention concerns also a method for
manufacturing a medicament intended for therapeutic application in
the said disease, characterized in that the pharmaceutical
composition according to the present invention is used.
[0139] A large dose range can be covered by varying the quantity of
the pharmaceutical composition of the invention and the active
ingredient load. Either immediate release (IR) or prolonged release
(PR) behavior can be achieved, as IR compositions are preliminary
to the PR compositions. Finally, the dissolution profile can be
easily modulated by varying the thickness of the PR coating.
Moreover, prolonged release multi-particulate forms generally offer
an enhanced robustness and reliability on the release profile of
the active ingredient.
[0140] The pharmaceutical composition of the invention releases at
least 50% of the active ingredient in less than 8 hours in order to
achieve acceptable drug absorption in vivo.
[0141] The following examples illustrate the invention without
however limiting its scope.
Example 1. Seletracetam Formulation
[0142] Low drug load pellets were prepared according to the
composition given in Table 1.
TABLE-US-00001 TABLE 1 Core compositions of Seletracetam pellets
with low drug load Step Material Quantity Step 1 First Cellets 700
98.5% layer Seletracetam 1.0% Disodium edetate 0.01% Pharmacoat 603
0.1% Talc 0.3% Step 2 Intermediate Pellets from step 1 90.9% layer
Pharmacoat 603 6.4% Talc 1.9% Polyethylene 0.7% glycol 6000 Step 3
Controlled Pellets from step 2 89.3% release Eudragit NE 30D 7.2%
coating Talc 3.1% Pharmacoat 606 0.4% Step 4 External Colloidal
anhydrous 0.50% relative process silica to final aid agent pellets
weight Step 5 Curing Pellets from step 4 are placed at 60.degree.
C. for 24 h
[0143] Microcrystalline core pellets (MCC spheres) are sold under
trade name Cellet.RTM.. The grade " 700 refers to a average
particle size ranging between 700 and 1000 .mu.m. Hydropropyl
methylcellulose (HPMC) sold under the trademark Pharmacoat.RTM. is
used as a binder agent. The grade 603 and 606 are preferred. Talc
is an antisticking agent. Disodium edetate is used as a
preservative agent. Polyethyleneglycol (PEG 6000) is a plasticiser
of Hydropropyl methylcellulose. The grade "6000" is preferred for
the application. It refers to an average molecular weight of 6000
da. Ethylacrylate-methylmethacrylate copolymer is sold under the
trademark Eudragit.RTM. NE 30D. Anhydrous colloidal silica is sold
under the trademark Aerosil.RTM. 200. it is used as antisticking
and gliding agent.
[0144] The obtained pellets show a sustained release profile for
Seletracetam, what comply with the in vitro dissolution
requirements.
TABLE-US-00002 TABLE 2 results in % Time Hours 1.00.00 4.00.00
16.00.00 Low drug load 21 53 100 pellets
[0145] The in vitro dissolution profiles in water were determined
according to the USP <711> (apparatus no 2, 50 rpm, aqueous
medium 500 ml) over an interval of time of 16 h. The dissolution
was conducted at 37.degree. C. in a pH 6.4 phosphate buffer.
Example 2. Seletracetam Formulation
[0146] Medium drug load pellets were prepared according to the
composition given in Table 3.
TABLE-US-00003 TABLE 3 Core compositions of Seletracetam pellets
with medium drug load Step Material Quantity Step 1 First Cellets
700 90.2% layer Seletracetam 7.0% Disodium edetate 0.1% Pharmacoat
603 0.7% Talc 2.1% Step 2 Intermediate Pellets from step 1 90.9%
layer Pharmacoat 603 6.4% Talc 1.9% Polyethylene 0.7% glycol 6000
Step 3 Controlled Pellets from step 2 88.9% release Eudragit NE 30D
7.5% coating Talc 3.2% Pharmacoat 606 0.4% Step 4 External
Colloidal anhydrous 0.50% relative process silica to final aid
agent pellets weight Step 5 Curing Pellets from step 4 are placed
at 60.degree. C. for 24 h
[0147] Microcrystalline core pellets are sold under trade name
Cellet.RTM.. The grade 700 refers to a average particle size
ranging between 700 and 1000 .mu.m. Hydropropyl methylcellulose
sold under the trademark Pharmacoat.RTM. is used as a binder agent.
The grade 603 and 606 are preferred. Talc is an antisticking agent.
Disodium edetate is used as a preservative agent.
Polyethyleneglycol (PEG 6000) is a plasticiser of hydropropyl
methylcellulose. The grade "6000" is preferred for the application.
It refers to an average molecular weight of 6000 da.
Ethylacrylate-methylmethacrylate copolymer is sold under the
trademark Eudragit.RTM. NE 30D. Anhydrous colloidal silica is sold
under the trademark Aerosil) 200. it is used as antisticking and
gliding agent.
[0148] The obtained pellets show a sustained release profile for
Seletracetam, what comply with the in vitro dissolution
requirements.
TABLE-US-00004 TABLE 4 results in % Time Hours 1.00.00 4.00.00
16.00.00 Medium drug load 27 63 101 pellets
[0149] The in vitro dissolution profiles in water were determined
according to the USP <711> (apparatus no 2, 50 rpm, aqueous
medium 900 ml) over an interval of time of 16 h. The dissolution
was conducted at 37.degree. C. in a pH 6.4 phosphate buffer.
Example 3. Seletracetam Formulation
[0150] High drug load pellets were prepared according to the
composition given in Table 5.
TABLE-US-00005 TABLE 5 Core compositions of Seletracetam pellets
with high drug load Step Material quantity Step 1 First Cellets 500
61.1% layer Seletracetam 27.5% Disodium edetate 0.4% Pharmacoat 603
2.8% Talc 8.3% Step 2 Intermediate Pellets from step 1 90.9% layer
Pharmacoat 603 6.4% Talc 1.9% Polyethylene 0.7% glycol 6000 Step 3
Controlled Pellets from step 2 81.3% release Eudragit NE 30D 12.5%
coating Talc 5.4% Pharmacoat 606 0.8% Step 4 External Colloidal
anhydrous 0.50% relative process silica to final aid agent pellets
weight Step 5 Curing Pellets from step 4 are paced at 60.degree. C.
for 24 h
[0151] Microcrystalline core pellets are sold under trade name
Cellet.RTM.. The grade 500 refers to a average particle size
ranging between 500 and 710 .mu.m. Hydropropyl methylcellulose sold
under the trademark Pharmcoat.RTM. is used as a binder agent. The
grade 603 and 606 are preferred. Talc is an antisticking agent.
Disodium edetate is used as a preservative agent.
Polyethyleneglycol (PEG 6000) is a plasticiser of hydropropyl
methylcellulose. The grade "6000" is preferred for the application.
It refers to an average molecular weight of 6000 da.
Ethylacrylate-methylmethacrylate copolymer is sold under the
trademark Eudragit.RTM. NE 30D. Anhydrous colloidal silica is sold
under the trademark Aerosil.RTM. 200. it is used as antisticking
and gliding agent.
[0152] The obtained pellets show a sustained release profile for
Seletracetam, what comply with the in vitro dissolution
requirements.
TABLE-US-00006 TABLE 6 results in % Time Hours 1.00.00 4.00.00
16.00.00 high drug load 16 65 100 pellets
[0153] The in vitro dissolution profiles in water were determined
according to the USP <711> (apparatus no 2, 50 rpm, aqueous
medium 900 ml) over an interval of time of 16 h. The dissolution
was conducted at 37.degree. C. in a pH 6.4 phosphate buffer.
Example 4: Brivaracetam Sustained Release Formulation
[0154] Brivaracetam pellets were prepared according to the
composition given in Table 7.
TABLE-US-00007 TABLE 7 Core compositions of Brivaracetam pellets
Step Material Quantity Step 1 Core Cellets 700 72% First
Brivaracetam 20.0% layer Pharmacoat 603 2.0% Talc 6.0% Step 2
Controlled Pellets from 83.3% step 2 release Eudragit NE 30D 11.2%
coating Talc 4.8% Pharmacoat 606 0.7% Step 3 External Colloidal
anhydrous 0.50% relative process silica to final aid agent pellets
weight Step 4 Curing Pellets from step 3 are placed at 50.degree.
C. for 24 h
[0155] Microcrystalline core pellets are sold under trade name
Cellet.RTM.. The grade 700 refers to a average particle size
ranging between 700 and 1000 .mu.m. Hydropropyl methylcellulose
sold under the trademark Pharmacoat.RTM. is used as a binder agent.
The grade 603 and 606 are preferred. Talc is an antisticking agent.
Ethylacrylate-methylmethacrylate copolymer is sold under the
trademark Eudragit.RTM. NE 30D. Anhydrous colloidal silica is sold
under the trademark Aerosil.RTM. 200. it is used as antisticking
and gliding agent.
[0156] The obtained pellets show a sustained release profile for
Brivaracetam what comply with the in vitro dissolution
requirements.
TABLE-US-00008 TABLE 8 results in % Time Hours 1.00.00 4.00.00
16.00.00 Brivaracetam 38 77 95 pellets
[0157] The in vitro dissolution profiles in water were determined
according to the USP <711> (apparatus no 2, 50 rpm, aqueous
medium 900 ml) over an interval of time of 16 h. The dissolution
was conducted at 37.degree. C. in a pH 6.4 phosphate buffer.
Example 5: Levetiracetam
[0158] Levetiracetam pellets were prepared according to the
composition given in Table 9
TABLE-US-00009 TABLE 9 Core compositions of Levetiracetam pellets
Step Material quantity Step 1 Core Cellets 700 72% First
Levetiracetam 20.0% layer Pharmacoat 603 2.0% Talc 6.0% Step 2
Controlled Pellets from step 2 80% release Eudragit NE 30D 13.9%%
coating Talc 5.4%% Pharmacoat 606 0.7%% Step 3 External Colloidal
anhydrous 0.50% relative process silica to final aid agent pellets
weight Step 4 Curing Pellets from step 3 are placed at 50.degree.
C. for 24 h
[0159] Microcrystalline core pellets are sold under trade name
Cellet.RTM.. The grade 700 refers to a average particle size
ranging between 700 and 1000 .mu.m. Hydropropyl methylcellulose
sold under the trademark Pharmacoat.RTM. is used as a binder agent.
The grade 603 and 606 are preferred. Talc is an antisticking agent.
Ethylacrylate-methylmethacrylate copolymer is sold under the
trademark Eudragit) NE 30D.
[0160] Anhydrous colloidal silica is sold under the trademark
Aerosil) 200. it is used as antisticking and gliding agent.
[0161] The obtained pellets show a sustained release profile for
Levetiracetam what comply with the in vitro dissolution
requirements.
TABLE-US-00010 TABLE 10 results in % Time Hours 1.00.00 4.00.00
16.00.00 Levetiracetam 1% 28% 99% pellets
[0162] The in vitro dissolution profiles in water were determined
according to the USP <711> (apparatus no 2, 50 rpm, aqueous
medium 900 ml) over an interval of time of 16 h. The dissolution
was conducted at 37.degree. C. in a pH 6.4 phosphate buffer.
Example 6: Pharmacological Data--: All Experiments were Performed
in Accordance with the Guidelines of the Local Ethical Committee
for Animal Experimentation
[0163] Epileptiform responses in hippocampal slices: Levetiracetam
reduces epileptiform responses induced in rat hippocampal slices by
high-K+/Iow-Ca2+ concentrations in the perfusion fluid and induced
by bicuculline. The effect of brivaracetam on epileptiform
responses induced by high-K+/Iow-Ca2+ concentrations or by
bicuculline was examined in transverse hippocampal slices prepared
from Sprague-Dawley rats according to previously reported standard
procedures. The epileptiform responses were induced by passing from
a normal perfusion of artificial cerebrospinal fluid (ACSF) (K+ 3
mM; Ca2+ 2.4 mM) to either high-K+/low-Ca2+ fluid (HKLCF) (K+ 7.5
mM; Ca2+ 0.5 mM) or to 5 M bicuculline methiodide (BMI)-containing
ACSF.
[0164] Extracellular field potentials (FPs) were recorded in the
CA3 area of the slices with 2 M NaCl-filled glass microelectrodes.
The evoked FPs were recorded at 10-min intervals in response to
fimbrial stimulation with constant current rectangular pulses that
elicit a single population spike (PS) of 50-75% of the maximal
amplitude when the slice is in ACSF. In the HKLCF model, 2 min of
spontaneous activity were also recorded, in the middle of each
10-min interval between the recordings of evoked responses.
[0165] Either brivaracetam or levetiracetam was added to the
bathing fluid of the slices 20 min before shifting from ACSF to
either HKLCF or 5 M BMI-containing ACSF, and was kept in the
perfusion fluid throughout the experiment.
[0166] Audiogenic seizures in mice: Genetically sound-sensitive
male mice (16-28 g; n=10 per group), responding with wild running,
clonic and tonic convulsions to an acoustic stimulation, were used.
Audiogenic seizures were induced by an acoustic stimulus (90 dB,
10-20 kHz) applied for 30 s. The mice were pretreated with either
saline, brivaracetam (i.p., 30 min) or levetiracetam (i.p., 60
min), and the proportion of mice protected against clonic
convulsions was used as the end point to assess anticonvulsant
activity.
[0167] Chemically induced seizures in mice:Pentylenetetrazol, 83 mg
kg-1 s.c., was used to evaluate the anticonvulsant properties of
brivaracetam. The dose was selected based on dose-effect curves in
saline-treated animals as the convulsive dose inducing clonic
convulsions of all four extremities in 97% of the animals.
Immediately after administration of the chemoconvulsant, the mice
were placed individually in small plastic cages (25 13 8 cm) and
observed for the presence of clonic convulsions in all four
extremities, for 60 min. The occurrence of tonic convulsions
(hindlimb extension) and mortality was also recorded during this
interval. The proportion of mice protected against clonic
convulsions was calculated and used as the end point for
anticonvulsant activity.
[0168] Results
[0169] Epileptiform responses in hippocampal slices: Changing the
perfusion of rat hippocampal slices from the normal ACSF to HKLCF
produced increasingly epileptiform FPs in the CA3 area in response
to constant-current fimbrial stimulation. In control slices exposed
to HKLCF alone, the PS1 amplitude progressively increased, reaching
plateau values within 20 min (4.250.77 mV), nearly twofold higher
than those recorded under ACSF perfusion (2.180.15 mV; means.d. for
n=10 slices). Also, constant-current single stimuli-evoked bursts
of repetitive PSs (that is, PS2, PS3 and so on) increased markedly
in number in the first 30 min of HKLCF perfusion from the single
PS1 to an average of 7.62.3 PS per evoked burst, and continued to
increase slightly up to the end of the records, reaching an average
of 8.81.6 PS per evoked burst after 80-min perfusion of HKLCF. Both
brivaracetam and levetiracetam reduced these epileptiform
responses. Upon 15-min perfusion of HKLCF, spontaneous field bursts
occurred in 4 out of the 10 control slices exposed to HKLCF alone,
whereas from 25 min in HKLCF to the end of the records, all control
slices presented regular field bursting. Brivaracetam (3.2 M), but
not levetiracetam (32 M), reduced the rate of this spontaneous
bursting.
[0170] In vivo studies: In fully amygdala-kindled rats,
brivaracetam induced a significant suppression in motor-seizure
severity from a dose of 21.2 mg kg-1, whereas levetiracetam induced
a similar effect from a dose of 170 mg kg-1. Brivaracetam also
significantly reduced the after-discharge duration at the highest
dose tested (212.3 mg kg-1), whereas levetiracetam was inactive on
this parameter up to 1700 mg kg-1.
[0171] Audiogenic seizure-susceptible mice were protected against
the expression of clonic convulsions by brivaracetam and
levetiracetam; ED50 values are shown in Table 2. Brivaracetam,
administered i.p. 30 min before seizure induction in mice, also
protected against clonic convulsions induced by pentylenetetrazol
and against tonic hindlimb extension induced by a maximal
electroshock in mice, although with higher ED50 values.
[0172] Brivaracetam significantly suppressed spontaneous SWDs in
GAERS rats from a dose of 2.1 mg kg-1 with complete inhibition
appearing at the highest dose tested (67.9 mg kg-1). Levetiracetam,
on the other hand, induced significant suppression of SWDs from a
dose of 5.4 mg kg-1.
[0173] Pretreatment with brivaracetam during corneal kindling of
mice resulted in a significant reduction in the incidence of
generalized motor seizures, and a similar incidence reduction was
observed with levetiracetam at higher doses. Continued corneal
stimulations following termination of treatment showed a persistent
reduction in the incidence of generalized motor seizures in the
group previously treated with the highest dose of brivaracetam.
* * * * *