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临床试验/EUCTR2014-003282-19-DE
EUCTR2014-003282-19-DE进行中(未招募)1 期

An Open Label, Randomized Phase 2 Trial of Pomalidomide/Dexamethasone With or Without Elotuzumab in relapsed and refractory Multiple Myeloma.

Bristol-Myers Squibb International Corporation0 个研究点目标入组 150 人开始时间: 2016年2月29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
150

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

  • (1) = 2 prior lines of therapy which must have included at least 2 consecutive cycles of lenalidomide and a proteosome inhibitor alone or in combination.
  • (2) Documented refractory or relapsed and refractory multiple myeloma
  • (3) Refractory to proteosome inhibitor and lenalidomide, and to their last treatment
  • (4) Relapsed and refractory patients had achieved at least a partial response to previous treatment with proteosome inhibitor or lenalidomide, or both, but progressed within 6 months, and were refractory to their last treatment.
  • (5) Measurable disease at screening
  • (6) Eastern Cooperative Oncology Group (ECOG) performance status = 2
  • 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 86
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 64

排除标准

  • (1) Active plasma cell leukemia
  • (2) Prior treatment with pomalidomide
  • (3) Unable to tolerate thromboembolic prophylaxis while on the study
  • (4) Prior autologous stem cell transplant within 12 weeks
  • (5) Known Human Immunodeficiency Virus (HIV) infection or active hepatitis A, B, or C

研究者

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