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临床试验/EUCTR2014-002372-89-BE
EUCTR2014-002372-89-BE进行中(未招募)1 期

A Phase 1/2 Multicenter Study of BMS-986012 in Subjects with Relapsed/Refractory Small Cell Lung Cancer

Bristol-Myers Squibb International Corporation0 个研究点目标入组 170 人开始时间: 2016年3月7日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
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 clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Histological or cytological confirmed SCLC
  • Performance Status 0-1
  • Adequate organ function
  • Measurable disease
  • 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 85
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 85

排除标准

  • Known or suspected brain metastasis
  • Small cell cancer not lung in origin
  • Significant or acute medical illness
  • Uncontrolled or significant cardiac disease
  • Infection
  • > Grade 2 peripheral neuropathy
  • Concomitant malignancies
  • HIV related disease or known or suspected HIV+
  • Hepatitis B or C infection
  • ECG abnormalities as defined by the protocol
  • Allergies or hypersensitivities to monoclonal antibodies, BMS-986012 or related compounds, including fucosyl-GM1 vaccine

研究者

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