跳至主要内容
临床试验/EUCTR2005-004105-28-GR
EUCTR2005-004105-28-GR进行中(未招募)不适用

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

PDL BioPharma, Inc.0 个研究点目标入组 300 人开始时间: 2007年2月15日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
300

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

  • 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.

研究者

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