Pharmaceutical formulation comprising a 2-aminoacetamide...

Drug – bio-affecting and body treating compositions – Solid synthetic organic polymer as designated organic active... – Ion exchange resin

Reexamination Certificate

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Details

C514S974000

Reexamination Certificate

active

06193962

ABSTRACT:

The present invention relates to novel formulations, in particular a formulation comprising an anticonvulsant and an ion-exchange resin.
European Patent Application No. 279937 describes a group of compounds which are NMDA antagonists and are indicated as anticonvulsants. EPA 279937 discloses the compound 2-amino-N-(1,2-diphenyl-1-methylethyl)acetamide hydrochloride (which has the INN remacemide hydrochloride). This compound is useful for the treatment of, inter alia, epilepsy, Parkinson's disease and Huntingdons disease.
Conventional liquid formulations of the above compound have a bitter and unpleasant taste which is a particular disadvantage for paediatric administration. Therefore there is a need for formulations containing remacemide which overcome this problem. Pharmaceutical formulations comprising a vasodilator in combination with an ion-exchange resins are known in the art, for example from EPA 501 763. There is no mention of other medicaments in combination with an ion-exchange resin. It has now surprisingly been found that if remacemide is combined with an ion-exchange resin the bitter taste of the resulting formulation is substantially eliminated. In addition to having a pleasant taste and mouthfeel, the formulations of the invention show good bioavailability.
In a first aspect the present invention therefore provides formulation comprising a compound of formula (I) or a salt thereof:
where:
R
1
and R
2
are independently phenyl or 4fluorophenyl;
R
3
is hydrogen, C
1-6
alkyl or methoxycarbonyl;
R
4
is hydrogen or methyl; in association with an ion-exchange resin and optionally further pharmaceutically acceptable carriers or excipients.
The preferred compound of formula (I) is 2-amino-N-(1,2-diphenyl-1-methylethyl)acetamide (remacemide) or a salt thereof, preferably the hydrochloride salt.
Examples of suitable ion exchange resins include acidic low cross-linked carboxylic acid resins prepared from methacrylic acid and divinyl benzene such as Amberlite IRP 64, IRP 69 and IRP 88. Preferably the ion exchange resin is Amberlite IRP64, Amberlite IRP-88, Purolite C115 KMR or Purolite C115 HMR. More preferably the ion exchange resin is Amberlite IRP-64 or Purolite C115 HMR, most preferably Amberlite IRP64. In the acidic conditions of the stomach the resin becomes fully un-ionised resulting in rapid release of the compound of formula (I). Preferably the level of resin present in the final suspension is about 3.0% w/v for a remacemide concentration of about 10 mg/ml, and about 6.0% w/v for a remacemide concentration of about 20 mg/ml.
In a further aspect the invention provides a compound of formula (I), in particular remacemide or a salt thereof, in the form of a complex with an ion exchange resin.
The formulations of the invention can be in the form of a suspension or a reconstitutable formulation suitable for reconstitution with a convenient volume of water or other palatable aqueous medium.
The viscosity of permanent suspensions of the invention can be increased by the addition of one or more hydrophillic polymers (viscosifiers). The addition of such polymers facilitates administration by improving mouthfeel and maintaining the suspension after shaking which ensures homogeneity and dose reproducibility. Preferred polymers are those that provide the desired rheological properties and give a good mouthfeel, including xanthan gum and microcrystalline cellulose/sodium carboxymethyl cellulose (Avicel). Additionally a protective colloid can be included in the formulation, for example xanthan gum, carboxymethyl cellulose or Methocel 90HG (hydroxypropylmethylcellulose). Preferably the colloid is added at about 15-20% of the hydrophillic polymer.
The suspensions of the invention can also contain a flocculant to prevent the resin forming a sediment which is non-redispersible. Preferred flocculants include cationic polymeric materials such as chitosan (Protosan).
Preferably the formulations of the invention are in the form of a reconstitutable formulation. The formulations of the invention are preferably supplied in dry powder form in individual bottles for reconstitution by the pharmacist.
Reconstitutable formlations of the invention can also contain viscosifiers as described above. Particularly suitable viscosifiers include Avicel and Keltrol.
If desired the resin can be milled to a selected the mean particle size, using, for example, centrifugal ball milling. However one advantage of the formulations of the invention is that milling of the resin is unecessary if the formulations contains an agent to improve mouthfeel, that is to say, eliminate the gritty texture of the resinate. If the need for milling is eliminated this is highly advantageous, since the resin can be difficult to mill on a large scale, and milling tends to increase methacrylic acid monomer levels in the case of Amberlite resin which is not desirable from a safety viewpoint. Suitable agents which improve mouthfeel include polyvinylpyrrolidine, in particular Kollidon 90F. The mouthfeel enhancer can be present in the range of about 0.1 to about 10% w/v, preferably about 1% to about 6% with a preferred maximum of about 2% for a paediatric formulation.
In a further aspect the invention therefore provides a pharmaceutical formulation comprising polyvinylpyrrolidine whereby the polyvinylpyrrolidine reduces the grittiness of the suspended particles enhancing palatability of the formulation.
The formulations of the invention can contain other pharmaceutically acceptable carriers or excipients.
Preservatives can be added to the formulations of the invention. Any preservative compatible with the formulation is suitable. Preferred preservatives include esters of hydroxybenzoic acid, in particular the commercial blend of methyl, ethyl and propyl esters known as Niasept. Niasept sodium is desirable for reconstitutable formulations since it is preferable that the formulation is cold water soluble.
The formulations of the invention can contain one or more flavourings. The flavouring substance may be any edible flavouring substance which is acceptable and approved for use with pharmaceutical formulations. Very many such substances are known. The flavouring substance may for example be a natural or artificial flavouring, such as of a fruit, vegetable or confectionery taste. Additionally or alternatively the flavouring substance may comprise a sweetener, such as sugar, or an artificial sweetner such as sodium saccharin or aspartame. In the case of paediatric formulations an artificial sweetner is preferred.
The formulations of the invention are suitable for the treatment or prophylaxis of disease conditions where administration of an NMDA antagonist is beneficial. Such conditions are listed in EPA 279937, EPA 356035, EPA 427 427, EPA 637956 and EPA 648489. In a further aspect the invention therefore provides a formulation as defined herein for use in therapy, and particularly for the treatment and prophylaxis of epilepsy, Parkinson's disease and Huntingdons disease. Preferably the formulations of the invention are used for the treatment and prophylaxis of epilepsy. As mentioned above, the reconstitutable formulations of the invention are particularly suitable for paediatric administration.
The invention also provides a formulation as defined herein for the treatment or prophylaxis of epilepsy. Suitable daily dose ranges are from about 1.0 mg/kg to about 50 mg/kg. Unit doses may be administered once or more than once a day, for example, 2, 3, or 4 times a day, more usually 1 or 2 times a day.


REFERENCES:
patent: 3100738 (1963-08-01), Cavallito
patent: 4714620 (1987-12-01), Bunick et al.
patent: 5334378 (1994-08-01), Mitani et al.
patent: 5626879 (1997-05-01), Anaebonam et al.
patent: 5643560 (1997-07-01), Bergwitz-Larsen et al.
patent: 0 279 937 A1 (1988-08-01), None
patent: 0 279 937 (1988-08-01), None
patent: 0 427 427 A2 (1991-05-01), None
patent: 0 435 684 A1 (1991-07-01), None
patent: 0 501 763 A1 (1992-09-01), None
patent: 0 564 154 A1 (1993-10-01), None
patent: 2 676 364 (1992-11-01), None
patent: 857194 (196

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