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临床试验/JPRN-jRCT2080223582
JPRN-jRCT2080223582已完成1 期

A Phase 1 Study of Cabiralizumab (BMS-986227, FPA008) Administered Alone or in Combination with Nivolumab (BMS-936558) in Advanced Malignancies

Bristol-Myers Squibb K.K.0 个研究点目标入组 36 人开始时间: 2017年7月5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
36

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
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • Performance status 0-1
  • Adequate organ function
  • Cohort M1, 2 and C1: Measurable disease
  • Cohort M1, M2 and C1: Subjects must have histologic or cytologic confirmation of an advanced (metastatic and/or unresectable) malignant solid tumor
  • Cohort C2: Documented refractory or relapsed multiple myeloma
  • Subjects must be refractory to or have relapsed after standard therapies, or have no known effective treatment

排除标准

  • Cohort M1, M2, and C1: Untreated or active central nervous system (CNS) or leptomeningeal metastases
  • Cohort M1, M2, and C1: Subjects with hepatocellular carcinoma (HCC)
  • Cohort C2: Subjects with solitary bone or extramedullary plasmacytoma as the only evidence of plasma cell dyscrasia

研究者

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