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临床试验/EUCTR2008-001823-71-IT
EUCTR2008-001823-71-IT进行中(未招募)不适用

Phase II study of the combination of Lenalidomide and Alemtuzumab as consolidation in patients who responded to a previus chemotherapeutic regimen administered for relapsed or refractory Chronic Lymphocytic Leukemia (CLL) - len-cam

Associazione Malattie Sangue ONLUS0 个研究点开始时间: 2008年5月20日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

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

  • - signed written informed consent
  • - age 18 years or older
  • - WHO performance status 0-II
  • - life expectancy > 6 months
  • - confirmation BCLL
  • - no major infection
  • 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
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - any serious medical condition or psychiatric illness
  • - pregnant or lactating women
  • - active secondary malignancy
  • - negativity for CD52 marker
  • - previous autologous or allogeneic stem cell transplant

研究者

发起方
Associazione Malattie Sangue ONLUS

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