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临床试验/JPRN-jRCT2080223357
JPRN-jRCT2080223357未知1 期

A Phase 1 Study of the Safety and Tolerability of BMS 986148 in Subjects With Advanced and/or Metastatic Solid Tumors

Bristol-Myers Squibb K.K.0 个研究点目标入组 15 人开始时间: 2016年10月24日最近更新:
适应症

试验速览

阶段
1 期
入组人数
15

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

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

入选标准

  • Subject with advanced and/or metastatic solid tumors which are expected to express mesothelin who received the previous treatment
  • Must have measurable tumor per Response Evaluation Criteria in Solid Tumors
  • (RECIST) or modified RECIST for malignant pleural mesothelioma
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1

排除标准

  • Cancer metastases in the brain
  • Uncontrolled or significant cardiovascular disease
  • Moderate eye disorders
  • Moderate peripheral neuropathy
  • Known past or active hepatitis B or C infection

研究者

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