CDK INHIBITOR SALTS
    82.
    发明授权
    CDK INHIBITOR SALTS 有权
    CDK抑制剂盐

    公开(公告)号:EP2424868B1

    公开(公告)日:2018-01-10

    申请号:EP10715240.7

    申请日:2010-04-23

    CPC分类号: C07D487/04

    摘要: The present invention relates to novel crystalline form(s) of water-soluble salts and of free base of a cdk inhibitor. Such crystal salts are for example fumarate, L-malate, maleate, succinate, adipate, malonate, glycolate, phosphate, mesylate, L-lactate, hydrochloride, di-hydrochloride, tri-hydrochloride. Hydrates and polymorphs of such new salt forms, a process for their preparation, their utility in therapy and to the pharmaceutical compositions containing them are also claimed and described in the present application.

    COMPOUNDS FOR TREATING PATIENTS WITH ROS1 MUTANT CANCER CELLS
    87.
    发明公开
    COMPOUNDS FOR TREATING PATIENTS WITH ROS1 MUTANT CANCER CELLS 审中-公开
    VERBINDUNGEN ZUR BEHANDLUNG VON PATIENTEN MIT MUTANTEN ROS1-KREBSZELLEN

    公开(公告)号:EP3107541A1

    公开(公告)日:2016-12-28

    申请号:EP15705613.6

    申请日:2015-02-19

    CPC分类号: A61K31/496

    摘要: Substituted indazole derivatives of formula (I) or formula 2.(I) and pharmaceutically acceptable salts thereof, as defined in the specification, process for their preparation and pharmaceutical compositions comprising them are disclosed; the compounds of the invention may be useful in therapy in the treatment of diseases associated with a deregulated protein kinase activity, like cancer.

    摘要翻译: 公开了本说明书中定义的式(I)或式(I)的取代的吲唑衍生物及其药学上可接受的盐,其制备方法和包含它们的药物组合物; 本发明的化合物可用于治疗与失调的蛋白激酶活性相关的疾病,如癌症。