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临床试验/JPRN-jRCT2080223369
JPRN-jRCT2080223369未知1 期

A Phase 1 Study of the Safety and Tolerability of BMS-986012 in Subjects With Small Cell Lung Cancer

Bristol-Myers Squibb K.K.0 个研究点目标入组 18 人开始时间: 2016年11月8日最近更新:
适应症

试验速览

阶段
1 期
入组人数
18

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 Endpoint Classification: Safety Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment

入排标准

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

入选标准

  • Histological or cytological confirmed small cell lung cancer (SCLC)
  • Eastern Cooperative Oncology Group Performance Status 0-1
  • at least one measurable lesion that is not amenable to resection.
  • Adequate organ function

排除标准

  • Symptomatic central nervous system (CNS) metastases
  • Greater than or equal to Grade 2 peripheral neuropathy
  • Uncontrolled or significant cardiac disease
  • Active or chronic infection with Human Immunodeficiency Virus(HIV), Hepatitis B Virus (HBV), or Hepatitis C Virus (HCV)

研究者

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