SOLID TAPENTADOL IN NON-CRYSTALLINE FORM
    1.
    发明申请
    SOLID TAPENTADOL IN NON-CRYSTALLINE FORM 审中-公开
    非结晶形式的固体TAPENTADOL

    公开(公告)号:US20130116333A1

    公开(公告)日:2013-05-09

    申请号:US13695433

    申请日:2011-05-05

    IPC分类号: A61K31/137

    摘要: The invention relates to solid tapentadol in non-crystalline form together with a surface stabiliser in the form of a stable intermediate. In the intermediate of the invention, tapentadol is preferably present in amorphous form or in the form of a solid solution. The invention further relates to methods of producing tapentadol in a solid, non-crystalline form and to pharmaceutical formulations containing solid, non-crystalline tapentadol.

    摘要翻译: 本发明涉及非结晶形式的固体他喷他多与稳定中间体形式的表面稳定剂。 在本发明的中间体中,他喷他多优选以无定形形式或固体形式存在。 本发明还涉及制备固体,非结晶形式的他喷他多和含有固体,非结晶的他喷他多的药物制剂的方法。

    COMPOSITION COMPRISING FESOTERODINE AND FIBER
    2.
    发明申请
    COMPOSITION COMPRISING FESOTERODINE AND FIBER 审中-公开
    包含FESOTERODINE和FIBER的组合物

    公开(公告)号:US20120258171A1

    公开(公告)日:2012-10-11

    申请号:US13501489

    申请日:2010-10-28

    IPC分类号: A61K31/222 A61K9/28 A61P13/10

    CPC分类号: A61K9/205 A61K31/222

    摘要: The invention relates to a pharmaceutical composition containing (a) fesoterodine and/or fesoterodine metabolites and (b) fibers, wherein the weight ratio of components (a):(b) is in the range from 1:50 to 1:2; and oral dosage forms containing the pharmaceutical composition. The invention further relates to dry methods of preparing those dosage forms.

    摘要翻译: 本发明涉及含有(a)非索罗定和/或非索罗定代谢物和(b)纤维的药物组合物,其中组分(a):(b)的重量比在1:50至1:2的范围内; 和含有药物组合物的口服剂型。 本发明还涉及制备这些剂型的干法。

    ORAL FORM OF ADMINISTRATION COMPRISING ENTECAVIR
    5.
    发明申请
    ORAL FORM OF ADMINISTRATION COMPRISING ENTECAVIR 审中-公开
    包含ENTECAVIR的管理形式

    公开(公告)号:US20120308652A1

    公开(公告)日:2012-12-06

    申请号:US13517981

    申请日:2010-12-22

    摘要: The invention relates to pharmaceutical formulations, preferably in the form of an oral dosage form, for the treatment of chronic hepatitis-B virus infections, containing micronised Entecavir, and processes for preparing it. The invention further relates to intermediates containing micronised entecavir, in which the D50 value for the particle size distribution is less than 50 μm, and processes for preparing them.

    摘要翻译: 本发明涉及用于治疗含有微粉化恩替卡韦的慢性乙型肝炎病毒感染的口服剂型形式的药物制剂及其制备方法。 本发明还涉及含有微粉化恩替卡韦的中间体,其中粒度分布的D50值小于50μm,以及制备它们的方法。