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临床试验/EUCTR2012-004502-93-PL
EUCTR2012-004502-93-PL进行中(未招募)1 期

An Open-Label, Randomized, Phase 3 Trial of Nivolumab versus Investigator's Choice Chemotherapy as First-Line Therapy for Stage IV or Recurrent PD-L1+ Non-Small Cell Lung Cancer - CheckMate 026: CHECKpoint pathway and nivoluMAb clinical Trial Evaluation 026

Bristol-Myers Squibb International Corporation0 个研究点目标入组 1,571 人开始时间: 2014年6月9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
1,571

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

入选标准

  • ECOG PS = 1
  • Histologically confirmed Stage IV, or Recurrent NSCLC with no prior systemic anticancer therapy
  • Measurable disease by CT or MRI per RECIST 1.1 criteria
  • PD-L1+ on immunohistochemistry testing performed by central lab
  • Men and women, ages = 18 years of age
  • 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 943
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 628

排除标准

  • Known EFGR mutations which are sensitive to available targeted inhibitor therapy
  • Known ALK translocations
  • Untreated CNS metastases
  • Previous malignancies
  • Active, known or suspected autoimmune disease

研究者

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