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临床试验/EUCTR2005-004105-28-IE
EUCTR2005-004105-28-IE
进行中(未招募)
1 期

An Observational Follow-up Study for Subjects Receiving Salvage Therapy After Previous Treatment in a Visilizumab Study for Intravenous Steroid-Refractory Ulcerative Colitis.

PDL BioPharma, Inc.0 个研究点目标入组 300 人2006年2月10日

概览

阶段
1 期
干预措施
未指定
疾病 / 适应症
未指定
发起方
PDL BioPharma, Inc.
入组人数
300
状态
进行中(未招募)
最后更新
5年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2006年2月10日
结束日期
待定
最后更新
5年前
研究类型
Interventional clinical trial of medicinal product
性别
All

研究者

入排标准

入选标准

  • Eligible subjects will be considered for inclusion in this study if they meet all of the following criteria:
  • 1\) Previous participation in an IVSR\-UC visilizumab study.
  • 2\) Disease progression while enrolled in a previous visilizumab study, and subsequent treatment with salvage therapy.
  • 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) yes
  • F.1\.3\.1 Number of subjects for this age range

排除标准

  • 1\) Unable to understand the purpose and risks of the study, or unwilling or unable to provide signed and dated informed consent.
  • 2\) For U.S. sites, unwilling or unable to provide authorization to use protected health information.

结局指标

主要结局

未指定

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