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临床试验/EUCTR2015-004816-39-NL
EUCTR2015-004816-39-NL进行中(未招募)1 期

A Phase 1/2a Study of BMS-986178 Administered Alone or in Combination with Nivolumab and/or Ipilimumab in subjects with Advanced Solid Tumors.

Bristol-Myers Squibb International Corporation0 个研究点目标入组 166 人开始时间: 2016年7月28日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
166

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

  • Subjects must be refractory to or intolerant of established therapy known to provide clinical benefit for their condition, i.e., subjects must not be candidates for regimens known to provide clinical benefit
  • ECOG (Eastern Cooperative Oncology Group) 0-1
  • Men and women 18 years old or older
  • At least one measurable lesion at baseline by CT (computed tomography) or MRI (magnetic resonance imaging) as per RECIST (Response Evaluation Criteria In Solid Tumors) v1.1
  • 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 247
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 357

排除标准

  • Known central nervous system metastases or central nervous system as the only source of disease
  • Concomitant malignancies
  • Active known or suspected autoimmune disease
  • Uncontrolled or significant cardiovascular disease
  • Major surgery less than 4 weeks before the start of the study

研究者

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