发明名称 |
Pharmaceutical compositions of selective factor Xa inhibitors for oral administration |
摘要 |
The present invention provides pharmaceutical compositions for oral administration comprising a therapeutically effective amount of a selective factor Xa inhibitor or a pharmaceutically acceptable salt thereof and an enhancer, wherein the enhancer is a medium chain fatty acid or a salt, ester, ether, or derivative of a medium chain fatty acid and has a carbon chain length of from about 4 to about 20 carbon atoms. The present invention also provides a method for obtaining a reproducible bioavailability of selective factor Xa inhibitor in an object after oral administration comprising orally administering a pharmaceutical composition as described above. |
申请公布号 |
US9089484(B2) |
申请公布日期 |
2015.07.28 |
申请号 |
US201113073202 |
申请日期 |
2011.03.28 |
申请人 |
Merrion Research III Limited |
发明人 |
Leonard Thomas W.;Coughlan David C.;Cullen Alan |
分类号 |
A61K8/21;A61K8/30;A61Q11/00;A61K9/107;A61K9/00;A61K31/715;A61K31/727;A61K47/12 |
主分类号 |
A61K8/21 |
代理机构 |
Myers Bigel Sibley & Sajovec, P.A. |
代理人 |
Myers Bigel Sibley & Sajovec, P.A. |
主权项 |
1. A method for obtaining a reproducible bioavailability of fondaparinux or a pharmaceutically acceptable salt thereof in a subject after oral administration, comprising orally administering to said subject a pharmaceutical composition comprising a therapeutically effective amount of fondaparinux or a pharmaceutically acceptable salt thereof and an enhancer, wherein the enhancer is a medium chain fatty acid salt and has a carbon chain length of from about 8 to about 14 carbon atoms, and wherein the bioavailability of fondaparinux or a pharmaceutically acceptable salt thereof has a coefficient of variation of no more than about 60%. |
地址 |
Dublin IE |