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Combined Therapy of anti-cd20 Antibody with an inhibitor of bcl-2, an inhibitor of MDM2, method of treatment, use

机译:抗cd20抗体与bcl-2抑制剂,MDM2抑制剂的联合疗法,治疗方法,用途

摘要

Combined Therapy of anti-cd20 Antibody with an inhibitor of bcl-2 and MDM2 inhibitor for the treatment of cancer, especially in the Combined Therapy of cancers that Express CD20 with an anti-cd20 Antibody of Type 1 or LY1 Humanized Antibody B - and not fucosilado inhibitor B CL - 2 and an inhibitor of MDM2.Claim 1: anti-cd20 Antibody for Cancer Treatment in combination with an inhibitor of bcl-2, an inhibitor of MDM2. Claim 5: Antibody according to any one of claims 1 to 4, characterized in that said not fucosilado anti-cd20 Antibody is an Antibody (LY1 Humanized.Claim 6: The Antibody according to any one of claims 1 to 5, characterized in that said anti-cd20 Antibody is not fucosilado obinutuzumab. Claim 7: Antibody according to any one of claims 1 to 5, characterized in that the anti-cd20 Antibody rituximab Type I is.Claim 8: The Antibody according to any one of claims 1 to 7, characterized in that the inhibitor of bcl-2 is 4 - (4 - [2 - (4-chlorophenyl) - 4.4 - dimetilciclohex - 1 - 1 - il] methyl} piperazin-1-yl) - 2 - (1h pyrrolo [2,3-b] pyridin - 5 - iloxi) - N - [4 - [(Tetrahydro - 2H - piran - 4 - methyl) amino] - 3 - [(trifluoromethyl) sulfonyl] phenyl] sulfonyl) benzamide.Claim no. 9: The Antibody according to any one of claims 1 to 7, characterized in that the MDM2 inhibitor is acid, 4 - [(2R, 3S, 4R, 5S) - 4 - (2 - Chloro - fluoro - phenyl) - 3 - (3 - Chloro - fluoro - 2 - cyano - 4 - phenyl) - 5 - (2,2-dimethyl - propyl) pyrrolidin-2-one carbonyl] amino} - 3 - metoxibienzoico.Claim 1: a Pharmaceutical composition comprising a combination of an anti-cd20 Antibody Type I or a B - LY1 Humanized Antibody that is without fucosilar fucose with a quantity of 60% or less of the total amount of Oligosaccharides (Sugars) in asn297, and 4 - (4 - [2 - (4 - clo Rofenil) - 4.4 - dimetilciclohex - 1 - 1 - il] methyl} piperazin-1-yl) - 2 - (1h pyrrolo [2,3 - B] pyridin - iloxi) - 5 - (N - (4 - [(Tetrahydro - 2H - piran - 4 - methyl) amino] - 3 - [(trifluoromethyl) sulfonyl] phenyl] sulfonyl) benzamide and acid, 4 - [(2R, 3S, 4R, 5S) - 4 - (4 - Chloro - fluoro - 2 - phenyl) - 3 - (3 - Chloro - fluoro - 2 - phenyl) - 5 - (4 - cyano - 2,2-dimethyl - propyl) pyrrolidin-2-one carbonyl] amino} - 3 - metoxibenzoico or a Salt of the same For the treatment of cancer.
机译:抗CD20抗体与bcl-2抑制剂和MDM2抑制剂的联合疗法,用于治疗癌症,尤其是在表达CD20与1型抗CD20抗体或LY1人源化抗体B的癌症的联合疗法中- fucosilado抑制剂B CL-2和MDM2抑制剂。声明1:抗cd20癌症治疗抗体与bcl-2抑制剂(MDM2抑制剂)联合使用。权利要求5:根据权利要求1至4中任一项所述的抗体,其特征在于,所述非岩藻抗cd20抗体是一种抗体(LY1人源化抗体)。权利要求6:根据权利要求1至5中任一项所述的抗体,其特征在于权利要求7:根据权利要求1至5中任一项的抗体,其特征在于抗CD20抗体I型利妥昔单抗是权利要求8:根据权利要求1至7中任一项的抗体。 ,其特征在于bcl-2的抑制剂是4-(4-[2--(4-氯苯基)-4.4-二甲氧基环己基-1-1-il]甲基}哌嗪-1-基)-2-(1h pyrrolo [ 2,3-b]吡啶-5-iloxi)-N-[4-[(四氢-2H-吡喃-4-甲基)氨基]-3-[[(三氟甲基)磺酰基]苯基]磺酰基)苯甲酰胺。 9.根据权利要求1至7中任一项所述的抗体,其特征在于,所述MDM2抑制剂是酸4-[(2R,3S,4R,5S)-4-(2-氯-氟-苯基)-3- (3-氯-氟-2-氰基-4-苯基)-5-(2,2-二甲基-丙基)吡咯烷基-2-一羰基]氨基}-3-甲氧西苯偶唑1.权利要求1:包含组合的药物组合物一种无fucosilar岩藻糖的I型抗cd20抗体或B-LY1人源化抗体,其含量为asn297中寡糖(糖)总量的60%或更少,以及4-(4-[2-( 4-clo Rofenil)-4.4-dimetilciclohex-1-1-il]甲基}哌嗪-1-基)-2-(1h吡咯并[2,3-B]吡啶-iloxi)-5-(N-(4- [(四氢-2H-吡喃-4-甲基)氨基]-3-[[(三氟甲基)磺酰基]苯基]磺酰基)苯甲酰胺和酸4-[((2R,3S,4R,5S)-4-(4-氯) -氟-2-苯基)-3-(3-氯-氟-2-苯基)-5-(4-氰基-2,2-二甲基-丙基)吡咯烷-2-酮[Onyl] amino}-3-metoxibenzoico或相同的盐用于治疗癌症。

著录项

  • 公开/公告号AR104735A1

    专利类型

  • 公开/公告日2017-08-09

    原文格式PDF

  • 申请/专利权人 F. HOFFMANN-LA ROCHE AG;

    申请/专利号AR2016P101500

  • 发明设计人

    申请日2016-05-24

  • 分类号A61K31/40;A61K31/496;A61K39/395;A61K45/06;A61P35;C07K16/28;C07K16/30;

  • 国家 AR

  • 入库时间 2022-08-21 13:40:58

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