Prolonged release formulations comprising an 2-oxo-1-pyrrolidine derivate
View Patent ↗The present invention relates to a pharmaceutical composition comprising Brivaracetam or Seletracetam as active ingredient, the invention relates specifically to a prolonged release formulation made of granules containing the active ingredient in their inner core.
1. A sustained release pharmaceutical composition comprising a granulate which contains an active ingredient and which is coated with a controlled release layer, wherein the active ingredient is brivaracetam or seletracetam.
2. The pharmaceutical composition according to claim 1 , wherein the active ingredient is brivaracetam.
3. The pharmaceutical composition according to claim 1 , wherein the weight percentage of the controlled release layer is comprised 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 contains at least a polymer consisting 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.
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 of 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 comprised 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 granulate is an active core which comprises the active ingredient and at least one excipient.
8. The pharmaceutical composition according to claim 7 , wherein the active core has a sphericity degree of between 0.5 and 1.0 and the average particle size of the active core is between 75 and 1400 μm.
9. The pharmaceutical composition according to claim 1 , wherein the granulate is coated with an intermediate layer.
10. The pharmaceutical composition according to claim 1 , wherein the granulate coated with the controlled release layer is further coated with the final layer.
11. The pharmaceutical composition according to claim 1 , further comprising an external phase.
12. The pharmaceutical composition according to claim 6 , wherein the excipient is a co-binder, an anti-sticking agent, an antifoam agent, a flavoring agent, a pigment, a plasticizer, an emulsifier, or a stabilizer.
13. The pharmaceutical composition according to claim 3 , wherein the active ingredient is brivaracetam.
14. The pharmaceutical composition according to claim 5 , wherein the active ingredient is brivaracetam.
15. The pharmaceutical composition according to claim 9 , wherein the active ingredient is brivaracetam.
16. The pharmaceutical composition according to claim 1 , wherein the release of the active ingredient in in vitro dissolution (USP<711>apparatus no2) in a buffered aqueous media is no more than 40% after 1 hour, 25%-80% after 4 hours, and no less than 80% after 16 hours.
17. The pharmaceutical composition according to claim 2 , wherein the release of the active ingredient in in vitro dissolution (USP<711>apparatus no2) in a buffered aqueous media is no more than 40% after 1 hour, 25%-80% after 4 hours, and no less than 80% after 16 hours.
18. The pharmaceutical composition according to claim 13 , wherein the release of the active ingredient in in vitro dissolution (USP<711>apparatus no2) in a buffered aqueous media is no more than 40% after 1 hour, 25%-80% after 4 hours, and no less than 80% after 16 hours.
19. The pharmaceutical composition according to claim 14 , wherein the release of the active ingredient in in vitro dissolution (USP<711>apparatus no2) in a buffered aqueous media is no more than 40% after 1 hour, 25% -80% after 4 hours, and no less than 80% after 16 hours.
20. The pharmaceutical composition according to claim 15 , wherein the release of the active ingredient in in vitro dissolution (USP<711>apparatus no2) in a buffered aqueous media is no more than 40% after 1 hour, 25% -80% after 4 hours, and no less than 80% after 16 hours.