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    • 8. 发明申请
    • Combination therapy for hyperproliferative disease
    • 过度增生性疾病的联合治疗
    • US20070197517A1
    • 2007-08-23
    • US10643546
    • 2003-08-19
    • Jitesh JaniJean BeebeTracey SchaefferDiane HealeyKaren FerranteJames O'Leary
    • Jitesh JaniJean BeebeTracey SchaefferDiane HealeyKaren FerranteJames O'Leary
    • A61K31/41A61K31/35A61K31/53C07D239/42
    • A61K31/282A61K31/337A61K31/425A61K31/427A61K31/454A61K31/473A61K31/4745A61K31/496A61K31/513A61K31/555A61K31/704A61K31/7048A61K2300/00
    • This invention relates a method of treating hyperproliferative diseases. More particularly, the present invention relates to a method of treating hyperproliferative diseases, such as cancer, comprising the step of administering to a mammal in need of such treatment, either simultaneously or sequentially, (i) a therapeutically effective amount of a taxane derivative, a platinium coordination complex selected from the group consisting of carboplatin, tetraplatin, and topotecan, a nucleoside analog selected from the group consisting of gemcitabine hydrochloride and 5-FU, an anthracycline, a topoisomerase selected from the group consisting of etoposide, teniposide, amsacrine, topotecan, and Camptosar®, an aromatase inhibitor; and (ii) a therapeutically effective amount of an isothiazole derivative. The combinations of the present invention may optionally include an anti-hypertensive agent. This invention also relates to pharmaceutical compositions useful in the treatment of hyperproliferative diseases in mammals, containing such combinations. The present invention also relates to kits having a first compartment with a compound of formula 1 and a second compartment containing a taxane derivative, a platinum coordination complex, a nucleoside analog, an anthracycline, a topoisomerase inhibitor, or an aromatase inhibitor and a third compartment containing an anti-hypertensive agent.
    • 本发明涉及一种治疗过度增殖性疾病的方法。 更具体地说,本发明涉及治疗过度增殖性疾病如癌症的方法,其包括以下步骤:同时或依次给予需要这种治疗的哺乳动物,(i)治疗有效量的紫杉烷衍生物, 选自卡铂,四铂和托泊替康的铂配位络合物,选自盐酸吉西他滨和5-FU的核苷类似物,蒽环类,拓扑异构酶,其选自依托泊苷,替尼泊苷,安吖啶, 拓扑替康和Camptosar(芳香酶抑制剂); 和(ii)治疗有效量的异噻唑衍生物。 本发明的组合可以任选地包括抗高血压剂。 本发明还涉及可用于治疗哺乳动物中含有这种组合的过度增殖性疾病的药物组合物。 本发明还涉及具有具有式1化合物的第一隔室和含有紫杉烷衍生物,铂配位络合物,核苷类似物,蒽环类,拓扑异构酶抑制剂或芳香酶抑制剂和第三隔室的第二隔室的试剂盒 含有抗高血压药。