跳至主要内容
临床试验/EUCTR2008-007969-23-IT
EUCTR2008-007969-23-IT进行中(未招募)1 期

A Phase 3 Study to Evaluate the Efficacy and Safety of Docetaxel and Prednisone with or without Lenalidomide in Subjects with Castrate-Resistant Prostate Cancer (CRPC)

Celgene Corporation0 个研究点目标入组 1,059 人开始时间: 2009年12月14日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
1,059

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
Male

入选标准

  • Screening and recruitment was completed under protocol amendment 2
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 317
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 742

排除标准

  • Screening and recruitment was completed under protocol amendment 2

研究者

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