发明名称 Combination antitumor therapy
摘要 The present disclosure relates to methods of treating cancers that are responsive to antimetabolite or antimitotic anti-cancer agents. The methods involve the use of at least one anti-cancer agent selected from antimetabolite anti-cancer agents, antimitotic anti-cancer agents, and combinations thereof, and a superoxide dismutase mimetic to potentiate the therapeutic effect of the anti cancer agent(s).
申请公布号 US9198893(B2) 申请公布日期 2015.12.01
申请号 US200912993140 申请日期 2009.05.22
申请人 GALERA LABS, LLC 发明人 Keene Jeffery L.;Riley Dennis P.;Beardsley Robert A.
分类号 A01N55/02;A61K31/28;A61K31/337;A61K45/06;A61K31/555 主分类号 A01N55/02
代理机构 Bryan Cave LLP 代理人 Bryan Cave LLP
主权项 1. A method of treating a cancer that is responsive to an antimetabolite or antimitotic anti-cancer agent in a mammalian subject afflicted with the cancer, the method comprising: administering to the subject at least one anti-cancer agent selected from antimetabolite anti-cancer agents, antimitotic anti-cancer agents, and combinations thereof, and a selective superoxide dismutase mimetic to potentiate the therapeutic effect of the anti-cancer agent(s); wherein the antimetabolite anti-cancer agent is selected from the group consisting of 2-fluorodeoxycytidine, 3′-azido-3′-deoxythymidine, 3′-deoxy-3′-deoxythymidin-2′-ene, 3′-dideoxycytidin-2′-ene, 3-fluoro-3′-deoxythymidine, 5-fluorocytosine, 5-fluorouracil, 5-methylcytosine, 5-propynylcytosine, 5-propynylthymine, 5-propynyluracil, 6-azauridine, 6-mercaptopurine, 8-aza-adenosine, 8-aza-guanosine, 8-fluoro-adenosine, acyclovir, allopurinol, ancitabine, arabinosyl adenine, azacitidine, azathiprine, bromouracil, capecitabine, carmofur, chlorouracil, cladribine, cytarabine, cytosine arabinoside, denopterin, deoxycoformycin, dideoxyuridine, dihydrouracil, doxifluridine, enocitabine, floxuridine, fludarabine, gancylovir, gemcitabine, methotrexate, pemetrexed, pentostatin, pteropterin, raltitrexed, thiamiprine, thioguanine, trimetrexate, salts thereof, and combinations thereof; the antimitotic anti-cancer agent is selected from the group consisting of docetaxel, epothilone A, epothilone B, epothilone C, epothilone D, epothilone E, epothilone F, paclitaxel, vinblastine, vincristine, vindesine, vinorelbine, salts thereof, and combinations thereof; wherein the selective superoxide dismutase mimetic has no significant activity toward hydrogen peroxide and corresponds to Formula (4419): wherein X and Y are ligands.
地址 St. Louis MO US