跳至主要内容
临床试验/EUCTR2006-001865-41-IT
EUCTR2006-001865-41-IT进行中(未招募)1 期

A phase III, Multicentre, Randomised, Double-Blind, Placebo controlled study to determine the efficacy and safety of lenalidomide (Revlimid in combination with Melphalan and Prednisone versus placebo plus melphalan and prednisone in subjects with newly diagnosed multiple myeloma who are 65 years of age or older - CC-5013-MM-015

Celgene0 个研究点目标入组 450 人开始时间: 2007年5月9日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
Celgene
入组人数
450

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

  • Able to understand and sign the ICF Aged at least 65 at time of ICF signature Newly diagnosed MM (according to three criteria)
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Previous treatment with antimyeloma therapy Any severe medical condition while in the study Pregnant or breastfeeding mothers

研究者

发起方
Celgene

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