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临床试验/EUCTR2016-003881-14-NO
EUCTR2016-003881-14-NO进行中(未招募)1 期

A Phase 3, Open-label, Randomized Study of Nivolumab Combined with Ipilimumab, or with Standard of Care Chemotherapy, versus Standard of Care Chemotherapy in Participants with Previously Untreated Unresectable or Metastatic Urothelial Cancer+ Protocol Amendment 07 specific to Norway dated 15-Dec-2017 - CheckMate 901: CHECKpoint pathway and nivoluMAb clinical Trial Evaluation 901

Bristol-Myers Squibb International Corporation0 个研究点目标入组 1,792 人开始时间: 2017年9月14日最近更新:
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试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
1,792

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • -Histological or cytological evidence of metastatic or surgically inoperable transitional cell cancer (TCC) of the urothelium involving the renal pelvis, ureter, bladder or urethra
  • -No prior systemic chemotherapy for metastatic or surgically inoperable urothelial cancer (UC)
  • -Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 or 1
  • -Women and men must agree to follow specific methods of contraception, if applicable
  • Other protocol-defined inclusion criteria apply
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 269
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 1523

排除标准

  • -Disease that is suitable for local therapy administered with curative intent
  • -Any serious or uncontrolled medical disorder in the opinion of the investigator that may increase the risk associated with study participation or study drug administration or interfere with the interpretation of study results
  • -Prior treatment with an anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or anti CTLA-4 antibody, or any other antibody or drug specifically targeting T-cell costimulation or checkpoint pathways
  • Other protocol-defined exclusion criteria apply

研究者

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