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COMBINED THERAPY, INCLUDING VEMURAFENIB AND INTERFERON, FOR USE IN TREATMENT OF CANCER

机译:联合治疗,包括维莫非尼和干扰素,用于癌症治疗

摘要

1. A pharmaceutical product containing (A) a first component that contains, as an active agent, {3- [5- (4-chloro-phenyl) -1H-pyrrolo [2,3-b] pyridin-3-carbonyl-2, 4-difluoro-phenyl] -amide} propan-1-sulfonic acid or a pharmaceutically acceptable salt thereof; and (B) a second component that contains interferon as an active agent; as a combined preparation for the simultaneous or sequential use in the treatment of a proliferative disease, in particular cancer, more specifically colorectal cancer, melanoma and thyroid cancer with b-Raf with a mutation V600.2. The pharmaceutical product of claim 1 for the simultaneous or sequential use in the treatment of a proliferative disease, in particular cancer, more specifically colorectal cancer, melanoma and thyroid cancer, with the presence of b-Raf with a mutation V600E. The pharmaceutical product according to claim 1 for simultaneous or sequential use in the treatment of melanoma containing b-Raf with a mutation V600E. The pharmaceutical product according to claim 1, wherein {3- [5- (4-chloro-phenyl) -1H-pyrrolo [2,3-b] pyridin-3-carbonyl-2,4-difluoro-phenyl] amide} propan-1-sulfonic acid or a pharmaceutically acceptable salt thereof is administered in an amount of from about 200 mg / day to about 3000 mg / day. The pharmaceutical product according to claim 1, wherein the {3- [5- (4-chloro-phenyl) -1H-pyrrolo [2,3-b] pyridin-3-carbonyl-2,4-difluoro-phenyl] amide propane -1-sulfonic acid or a pharmaceutically acceptable salt thereof is administered in an amount of from about 1700 mg / day to about 2100 mg / day. The pharmaceutical product according to claim 1, wherein said interferon is peginterferon alfa-2a. The pharmaceutical product according to claim 6, in which
机译:1.一种药物产品,其包含(A)第一成分,该第一成分包含{3- [5-(4-氯-苯基)-1H-吡咯并[2,3-b]吡啶-3-羰基- 2,4-二氟-苯基]-酰胺}丙-1-磺酸或其药学上可接受的盐; (B)第二成分,其含有干扰素作为活性剂;作为同时或相继用于治疗增生性疾病(尤其是癌症,更具体而言是大肠癌,黑素瘤和甲状腺癌)的突变型b-Raf的联合制剂,其突变V600.2。权利要求1的药物产品,用于同时或相继用于治疗具有突变V600E的b-Raf的增生性疾病,特别是癌症,尤其是结肠直肠癌,黑素瘤和甲状腺癌。 2.根据权利要求1的药物产品,用于同时或相继用于治疗含有突变为V600E的b-Raf的黑色素瘤。 2.根据权利要求1的药物,其中{3- [5-(4-氯-苯基)-1H-吡咯并[2,3-b]吡啶-3-羰基-2,4-二氟-苯基]酰胺}丙烷-1-磺酸或其药学上可接受的盐以约200mg /天至约3000mg /天的量施用。 2.根据权利要求1的药物,其中{3- [5-(4-氯-苯基)-1H-吡咯并[2,3-b]吡啶-3-羰基-2,4-二氟-苯基]酰胺丙烷-1-磺酸或其药学上可接受的盐的施用量为约1700 mg /天至约2100 mg /天。 2.根据权利要求1所述的药物,其中,所述干扰素为聚乙二醇干扰素α-2a。 7.根据权利要求6所述的药品,其中,

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