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临床试验/EUCTR2017-000367-33-FR
EUCTR2017-000367-33-FR进行中(未招募)1 期

Phase 1/2 Study to Evaluate the Safety and Preliminary Efficacy of Nivolumab Combined with Daratumumab in Participants with Advanced or Metastatic Solid Tumors

Bristol-Myers Squibb International Corporation0 个研究点目标入组 105 人开始时间: 2017年7月27日最近更新:
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试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
105

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

  • - Patients must have metastatic or advanced solid tumors.
  • - Women with histologically or cytologically confirmed triple negative breast carcinoma.
  • - Participants with histologically confirmed pancreatic adenocarcinoma.
  • - Participants must have histologic or cytologic confirmation of Non Small Cell Lung Cancer (NSCLC).
  • 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 66
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 94

排除标准

  • -Active brain metastases or leptomeningeal metastases.
  • - Any serious or uncontrolled medical disorder.
  • - Prior malignancy active within the previous 3 years.

研究者

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