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临床试验/EUCTR2021-003208-42-BE
EUCTR2021-003208-42-BE进行中(未招募)1 期

A Phase 3, Open Label, Randomized, Non-Inferiority Pharmacokinetic Study of Nivolumab Subcutaneous (Nivo SC) Versus Intravenous (Nivo IV) Administration in Participants with Stage IIIA/B/C/D or Stage IV Adjuvant Melanoma Following Complete Resection - CheckMate-6GE: CHECKpoint pathway and nivoluMAb clinical Trial Evaluation 6GE

Bristol-Myers Squibb International Corporation0 个研究点目标入组 379 人开始时间: 2022年3月17日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
379

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • Not applicable per Protocol Amendment 01 (as of 24-Feb-2023, enrollment in this study has closed).
  • 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 276
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 103

排除标准

  • Not applicable per Protocol Amendment 01 (as of 24-Feb-2023, enrollment in this study has closed).

研究者

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