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公开(公告)号:WO2006091529A2
公开(公告)日:2006-08-31
申请号:PCT/US2006/005944
申请日:2006-02-21
Applicant: ABBOTT LABORATORIES , ROSENBERG, Jöerg , REINHOLD, Ulrich , LIEPOLD, Bernd , BERNDL, Gunther , BREITENBACH, Jörg , ALANI, Laman , GHOSH, Soumojeet
Inventor: ROSENBERG, Jöerg , REINHOLD, Ulrich , LIEPOLD, Bernd , BERNDL, Gunther , BREITENBACH, Jörg , ALANI, Laman , GHOSH, Soumojeet
IPC: A61K31/513 , A61K31/426 , A61K9/20 , A61K9/28
CPC classification number: A61K9/1694 , A61K9/1617 , A61K9/1635 , A61K9/2009 , A61K9/2013 , A61K9/2018 , A61K9/2027 , A61K9/2031 , A61K9/204 , A61K9/2077 , A61K9/2095 , A61K9/2866 , A61K31/00 , A61K31/426 , A61K31/427 , A61K31/513 , A61K47/32 , A61K2300/00
Abstract: The present invention provides a pharmaceutical dosage formulation, and more particularly, to a pharmaceutical dosage formulation comprising an HIV protease inhibitor.
Abstract translation: 本发明提供药物剂型制剂,更具体地说,涉及包含HIV蛋白酶抑制剂的药物剂型。
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公开(公告)号:WO2005039551A2
公开(公告)日:2005-05-06
申请号:PCT/US2004/027401
申请日:2004-08-23
Applicant: ABBOTT LABORATORIES , ROSENBERG, Jöerg , REINHOLD, Ulrich , LIEPOLD, Bernd , DERNDL, Gunther , BREITENBACH, Jörg , ALANI, Laman , GHOSH, Soumojeet
Inventor: ROSENBERG, Jöerg , REINHOLD, Ulrich , LIEPOLD, Bernd , DERNDL, Gunther , BREITENBACH, Jörg , ALANI, Laman , GHOSH, Soumojeet
IPC: A61K31/00
CPC classification number: A61K31/425 , A61K9/146 , A61K9/2009 , A61K9/2013 , A61K9/2027 , A61K9/2866
Abstract: A solid pharmaceutical dosage form providing improved oral bioavailability is disclosed for inhibitors of HIV protease. In particular, the dosage form comprises a solid dispersion of at least one HIV protease inhibitor and at least one pharmaceutically acceptable water-soluble polymer and at least one pharmaceutically acceptable surfactant, said pharmaceutically acceptable water-soluble polymer having a Tg of at least about 50 °C. Preferably, the pharmaceutically acceptable surfactant has an HLB value of from about 4 to about 10.
Abstract translation: 公开了提供改善的口服生物利用度的固体药物剂型,用于HIV蛋白酶的抑制剂。 特别地,剂型包含至少一种HIV蛋白酶抑制剂和至少一种药学上可接受的水溶性聚合物和至少一种药学上可接受的表面活性剂的固体分散体,所述药学上可接受的水溶性聚合物的Tg至少为约50 C。 优选地,药学上可接受的表面活性剂具有约4至约10的HLB值。
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公开(公告)号:EP1855683A2
公开(公告)日:2007-11-21
申请号:EP06735552.9
申请日:2006-02-21
Applicant: ABBOTT LABORATORIES
Inventor: ROSENBERG, Jöerg , REINHOLD, Ulrich , LIEPOLD, Bernd , BERNDL, Gunther , BREITENBACH, Jörg , ALANI, Laman , GHOSH, Soumojeet
IPC: A61K31/513 , A61K31/426 , A61K9/20 , A61K9/28
CPC classification number: A61K9/1694 , A61K9/1617 , A61K9/1635 , A61K9/2009 , A61K9/2013 , A61K9/2018 , A61K9/2027 , A61K9/2031 , A61K9/204 , A61K9/2077 , A61K9/2095 , A61K9/2866 , A61K31/00 , A61K31/426 , A61K31/427 , A61K31/513 , A61K47/32 , A61K2300/00
Abstract: The present invention provides a pharmaceutical dosage formulation, and more particularly, to a pharmaceutical dosage formulation comprising an HIV protease inhibitor.
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公开(公告)号:EP1663183A2
公开(公告)日:2006-06-07
申请号:EP04816820.7
申请日:2004-08-23
Applicant: ABBOTT LABORATORIES
Inventor: ROSENBERG, Jöerg , REINHOLD, Ulrich , LIEPOLD, Bernd; , DERNDL, Gunther , BREITENBACH, Jörg , ALANI, Laman , GHOSH, Soumojeet
IPC: A61K31/00
CPC classification number: A61K31/425 , A61K9/146 , A61K9/2009 , A61K9/2013 , A61K9/2027 , A61K9/2866
Abstract: A solid pharmaceutical dosage form providing improved oral bioavailability is disclosed for inhibitors of HIV protease. In particular, the dosage form comprises a solid dispersion of at least one HIV protease inhibitor and at least one pharmaceutically acceptable water-soluble polymer and at least one pharmaceutically acceptable surfactant, said pharmaceutically acceptable water-soluble polymer having a Tg of at least about 50 °C. Preferably, the pharmaceutically acceptable surfactant has an HLB value of from about 4 to about 10.
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公开(公告)号:EP1663183B1
公开(公告)日:2011-07-13
申请号:EP04816820.7
申请日:2004-08-23
Applicant: ABBOTT LABORATORIES
Inventor: ROSENBERG, Jöerg , REINHOLD, Ulrich , LIEPOLD, Bernd , DERNDL, Gunther , BREITENBACH, Jörg , ALANI, Laman , GHOSH, Soumojeet
IPC: A61K9/14 , A61K31/425 , A61K9/20
CPC classification number: A61K31/425 , A61K9/146 , A61K9/2009 , A61K9/2013 , A61K9/2027 , A61K9/2866
Abstract: A solid pharmaceutical dosage form providing improved oral bioavailability is disclosed for inhibitors of HIV protease. In particular, the dosage form comprises a solid dispersion of at least one HIV protease inhibitor and at least one pharmaceutically acceptable water-soluble polymer and at least one pharmaceutically acceptable surfactant, said pharmaceutically acceptable water-soluble polymer having a Tg of at least about 50 °C. Preferably, the pharmaceutically acceptable surfactant has an HLB value of from about 4 to about 10.
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公开(公告)号:EP1663183B9
公开(公告)日:2012-06-13
申请号:EP04816820.7
申请日:2004-08-23
Applicant: ABBOTT LABORATORIES
Inventor: ROSENBERG, Jöerg , REINHOLD, Ulrich , LIEPOLD, Bernd , DERNDL, Gunther , BREITENBACH, Jörg , ALANI, Laman , GHOSH, Soumojeet
IPC: A61K9/14 , A61K31/425 , A61K9/20
CPC classification number: A61K31/425 , A61K9/146 , A61K9/2009 , A61K9/2013 , A61K9/2027 , A61K9/2866
Abstract: A solid pharmaceutical dosage form providing improved oral bioavailability is disclosed for inhibitors of HIV protease. In particular, the dosage form comprises a solid dispersion of at least one HIV protease inhibitor and at least one pharmaceutically acceptable water-soluble polymer and at least one pharmaceutically acceptable surfactant, said pharmaceutically acceptable water-soluble polymer having a Tg of at least about 50 °C. Preferably, the pharmaceutically acceptable surfactant has an HLB value of from about 4 to about 10.
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