US2016250147A1PendingUtilityA1
Solid Pharmaceutical Compositions Containing Pregabalin
Est. expiryNov 2, 2025(expired)· nominal 20-yr term from priority
Inventors:Howard N. BockbraderYun Hyung ChoSteven Diaz SantiagoMajid MahjourThomas Daniel ReynoldsPushpa Ganapathi ShaoZezhi Jesse ShaoJiansheng Wan
A61P 25/36A61P 25/18A61P 25/20A61P 29/00A61P 25/22A61P 25/00A61P 25/32A61P 25/08A61P 25/04A61P 25/24A61P 25/02A61P 1/00A61P 1/04A61K 9/141A61K 9/2027A61K 47/32A61K 31/197A61K 9/146A61K 47/34A61K 2039/542A61K 9/0053A61K 9/0065A61K 47/30A61K 9/20
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Abstract
A solid pharmaceutical composition containing pregabalin is described. The composition includes a matrix forming agent and a swelling agent and is suitable for once daily oral administration. Exemplary matrix forming agents include mixtures of polyvinyl acetate and polyvinylpyrrolidone, and exemplary swelling agents include cross-linked polymers of polyvinylpyrrolidone.
Claims
exact text as granted — not AI-modified1 - 15 . (canceled)
16 . A pharmaceutical composition comprising an active pharmaceutical ingredient and excipients, the active pharmaceutical ingredient comprising pregabalin, or a pharmaceutically acceptable complex, salt, solvate or hydrate thereof, and the excipients comprising a matrix forming agent and a swelling agent, the matrix forming agent comprising polyvinyl acetate and polyvinylpyrrolidone, and the swelling agent comprising crosslinked polyvinylpyrrolidone, wherein the pharmaceutical composition is adapted for once-daily oral dosing; wherein the pregabalin comprises from about 5% to about 60% of the pharmaceutical composition by weight; the matrix forming agent comprises from about 5% to about 45% of the pharmaceutical composition by weight, and the swelling agent comprises from about 15% to about 70% of the pharmaceutical composition by weight.
17 . The pharmaceutical composition according to claim 16 in which:
a) said matrix forming agent comprises about 20% to about 35% of the pharmaceutical composition by weight, and;
b) said swelling agent comprises about 20% to about 55% of the pharmaceutical composition by weight.
18 . The formulation according to claim 16 in which the polyvinyl acetate is present in the quantity of about 60% to about 90% by weight based on the total weight of the polyvinyl acetate and polyvinylpyrrolidone.
19 . The formulation according to claim 16 in which the polyvinyl acetate is present in the quantity of about 70% to about 90% by weight based on the total weight of the polyvinyl acetate and polyvinylpyrrolidone.
20 . A pharmaceutical formulation suitable for once-a-day administration comprising:
a) pregabalin, or a pharmaceutically acceptable complex, salt, solvate or hydrate thereof, present in the quantity of from about 5% to about 60%, based on the total weight of the formulation; b) a matrix of polyvinyl acetate and polyvinylpyrrolidone, in which the polyvinyl acetate is present in the quantity of about 70% to about 90% based on the total weight of the polyvinyl acetate and polyvinylpyrrolidine and the matrix is present in the quantity of about 20% to 35% by weight, based on the total weight of the formulation, and; c) cross linked polyvinylpyrrolidone, present in the quantity of about 10% to about 35% by weight, based on the total weight of the formulation.
21 . The formulation according to claim 20 in which the cross linked polyvinylpyrrolidone is present in the quantity of from about 20% to about 30% by weight, based on the total weight of the formulation.Cited by (0)
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