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临床试验/JPRN-jRCT2080223478
JPRN-jRCT2080223478已完成1 期

Phase 1/2a First-In-Human Study of BMS-986207 Monoclonal Antibody Alone and in Combination With Nivolumab in Advanced Solid Tumors

Bristol-Myers Squibb K.K.0 个研究点目标入组 170 人开始时间: 2017年3月14日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
170

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-Randomized Intervention Model: Parallel Assignment Masking: No masking Primary Purpose: Treatment

入排标准

年龄范围
>= 18age old 至 ot applicable(—)
性别
All

入选标准

  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Must have received and progressed on or failed one standard/approved treatment for cancer type, if available
  • At least 4 weeks since any previous treatment for cancer
  • Subject must consent to pretreatment and on treatment tumor biopsies
  • At least one lesion with measurable disease at baseline

排除标准

  • Patients with primary brain tumors or primary tumors with central nervous system metastases as only location of disease. Controlled brain metastases are permitted
  • Prior organ transplant
  • Participants with second/other active cancers requiring current treatment
  • Uncontrolled/significant heart disease
  • History of chronic hepatitis, Positive test for Hepatitis B virus surface antigen or Hepatitis C antibody (except participants with liver cancer) or Human Immunodeficiency Virus/Acquired Immunodeficiency Syndrome(HIV/AIDS)
  • Active/uncontrolled autoimmune disease
  • Active infection

研究者

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