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临床试验/EUCTR2016-003536-21-ES
EUCTR2016-003536-21-ES进行中(未招募)1 期

Randomized, Open-Label, Phase 3 Trial of Nivolumab and Ipilimumab versus Platinum-Doublet Chemotherapy in Early Stage NSCLC - CheckMate 816: CHECKpoint pathway and nivoluMAb clinical Trial Evaluation 816

Bristol-Myers Squibb International Corporation0 个研究点目标入组 326 人开始时间: 2016年12月27日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
326

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

  • Early stage (IB - IIIA), operable non-small cell lung cancer, confirmed in tissue.
  • Lung function capacity capable of tolerating the proposed lung surgery
  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1
  • Available tissue of primary lung tumor.
  • 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 126
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 200

排除标准

  • Presence of locally advanced, inoperable or metastatic disease.
  • Participants with active, known or suspected autoimmune disease.
  • Prior treatment with any drug that targets T cell co-stimulations pathways (such as checkpoint inhibitors).

研究者

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