Solid dosage form of HIV protease inhibitors
    1.
    发明公开
    Solid dosage form of HIV protease inhibitors 审中-公开
    Feste Dosierungsformen von HIV-Proteaseinhibitoren

    公开(公告)号:EP2564832A1

    公开(公告)日:2013-03-06

    申请号:EP11179139.8

    申请日:2011-08-29

    申请人: Hexal AG

    摘要: A pharmaceutical dosage form suitable for oral administration comprising a solid dispersion of at least one HIV protease inhibitor, at least one first pharmaceutically acceptable water-soluble polymer (A), at least one second pharmaceutically acceptable water-soluble polymer (B), and optionally at least one pharmaceutically acceptable surfactant,wherein the at least one first pharmaceutically acceptable water-soluble polymer (A) has a glass transition temperature (Tg) of at least 50°C and is present in an amount of 10% to 49% by weight of the dosage form and is not polyvinylpyrrolidone (PVP) or hydroxypropyl methylcellulose (HPMC), and wherein the at least one second pharmaceutically acceptable water-soluble polymer (B) has a Tg of less than 50°C.

    摘要翻译: 适合于口服给药的药物剂型,其包含至少一种HIV蛋白酶抑制剂,至少一种第一药学上可接受的水溶性聚合物(A),至少一种第二药学上可接受的水溶性聚合物(B)和任选地 至少一种药学上可接受的表面活性剂,其中所述至少一种第一药学上可接受的水溶性聚合物(A)的玻璃化转变温度(Tg)为至少50℃,并且以10重量%至49重量% 并且不是聚乙烯吡咯烷酮(PVP)或羟丙基甲基纤维素(HPMC),并且其中所述至少一种第二药学上可接受的水溶性聚合物(B)的Tg小于50℃。