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临床试验/EUCTR2014-002485-70-GB
EUCTR2014-002485-70-GB进行中(未招募)1 期

A Phase I/IIa Study of BMS 986148, a Mesothelin Directed Antibody Drug Conjugate, in Subjects with Select Advanced Solid Tumors

Bristol-Myers Squibb International Corporation0 个研究点目标入组 301 人开始时间: 2016年4月19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
301

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

  • Must have pancreatic, ovarian, gastric, non-small cell cancer or mesothelioma. For dose expansion, must have tumor that is positive for mesothelin
  • Expected to have life expectancy of at least 3 months
  • Men and women 18 years old or older
  • Must have measurable tumor per Response Evaluation Criteria In Solid Tumors (RECIST) or modified RECIST for malignant pleural mesothelioma
  • ECOG of 0 to 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 117
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 184

排除标准

  • Cancer metastases in the brain
  • Moderate eye disorders
  • Active infection or past hepatitis B or C infection
  • Major surgery less than 1 month before the start of the study
  • Uncontrolled heart disease
  • Impaired liver or bone marrow function

研究者

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