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临床试验/EUCTR2018-000416-21-ES
EUCTR2018-000416-21-ES进行中(未招募)1 期

A Phase 1/2 First-in-Human Study of BMS-986249 Alone and in Combination with Nivolumab in Advanced Solid Tumors

Bristol-Myers Squibb International Corporation0 个研究点目标入组 300 人开始时间: 2018年8月10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
300

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

  • _Participants must be at least 18 years old;
  • _have histologic or cytologic confirmation of a solid tumor that is advanced (metastatic, recurrent, and/or unresectable) with measurable disease
  • _Have at least 1 lesion accessible for biopsy;
  • _Eastern Cooperative Oncology Group Performance Status of 0 or 1;
  • _Participants must have received, and then progressed, relapsed, or been intolerant to, at least 1 standard treatment regimen in the advanced or metastatic setting according to solid tumor histologies.
  • 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 225
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 75

排除标准

  • _Participants with primary CNS malignancies or tumors with CNS metastases as the only site of disease;
  • _Participants with other active malignancy requiring concurrent intervention;

研究者

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A Phase 1/2 First-in-Human Study of BMS-986249 Alone... | 临床试验