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临床试验/EUCTR2014-002407-25-BE
EUCTR2014-002407-25-BE进行中(未招募)1 期

A Phase 4 long-term follow-up study to define the safety profile of radium-223 dichloride - Radium-223 dichloride long-term follow-up program

Bayer AG0 个研究点目标入组 800 人开始时间: 2018年9月10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)
发起方
Bayer AG
入组人数
800

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. Subject was previously enrolled in a selected company-sponsored feeder trial, and has received at least 1 dose of radium-223 dichloride or placebo in the feeder trial.
  • 2. Written informed consent.
  • 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 400
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 400

排除标准

  • Not applicable for this study

研究者

发起方
Bayer AG

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