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临床试验/EUCTR2016-001514-20-CZ
EUCTR2016-001514-20-CZ进行中(未招募)1 期

A Randomized Phase 3 Study of Nivolumab plus Ipilimumab or Nivolumab Combined with Fluorouracil plus Cisplatin versus Fluorouracil plus Cisplatin in Subjects with Unresectable Advanced, Recurrent or Metastatic Previously Untreated Esophageal Squamous Cell Carcinoma - CheckMate 648

Bristol-Myers Squibb International Corporation0 个研究点目标入组 1,127 人开始时间: 2016年10月17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
1,127

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

  • - Must have histologically confirmed squamous cell carcinoma or adenosquamous cell carcinoma of esophagus
  • - Male or Female at least 18 years of age
  • - Must have esophageal cancer that cannot be operated on, or treated with definitive chemoradiation with curative intent, that is advanced, reoccurring or has spread out
  • - Must have full activity or, if limited, must be able to walk and carry out light activities such as light house work or office work
  • - Must agree to provide tumor tissue sample, either from a previous surgery or biopsy within 6 months or fresh, prior to the start of treatment
  • in this study
  • 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 451
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 676

排除标准

  • - Presence of tumor cells in the brain or spinal cord which are symptomatic or require treatment.
  • - Active known or suspected autoimmune disease
  • - Any serious or uncontrolled medical disorder or active infection
  • - Known history of positive test for human immunodeficiency virus (HIV) or known acquired immunodeficiency syndrome (AIDS)
  • - Any positive test result for hepatitis B or C indicating acute or chronic infection and/or detectable virus.

研究者

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