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临床试验/EUCTR2015-004914-79-ES
EUCTR2015-004914-79-ES进行中(未招募)1 期

A Phase 1/2a Study of BMS-986205 Administered in Combination With Nivolumab (BMS-936558, Anti-PD-1 Monoclonal Antibody) in Advanced Malignant Tumors

Bristol-Myers Squibb International Corporation0 个研究点目标入组 288 人开始时间: 2016年8月5日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
288

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

  • Patients must have been diagnosed with cancer and had at least 1 prior standard treatment
  • Must be able to swallow pills or capsules
  • Eastern Cooperative Oncology Group(ECOG) Performance Status 0-1
  • 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 173
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 115

排除标准

  • Any prior ongoing clinical study with Nivolumab with overall survival as an endpoint
  • Requirement for daily supplemental oxygen
  • Myocardial infarction or stroke/transient ischemic attack within the past 6 months
  • Uncontrolled angina within the past 3 months
  • History of any chronic Hepatitis, active Hepatitis B or C, human immunodeficiency virus(HIV), or acquired immune deficiency syndrome(AIDS)

研究者

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