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临床试验/EUCTR2011-004810-41-DE
EUCTR2011-004810-41-DE进行中(未招募)不适用

An international, multicenter, open-label study evaluating sustained virological response and safety with Boceprevir in triple combination therapy with Peginterferon alfa-2a (40KD) and Ribavirin in treatment-naïve patients with genotype 1 chronic hepatitis C. - TRICO

F. Hoffmann-La Roche Ltd0 个研究点目标入组 150 人开始时间: 2012年6月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
150

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

  • Treatment-naïve adult women and men with chronic hepatitis C monoinfection, genotype 1 and compensated liver disease including cirrhosis
  • 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 142
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 8

排除标准

  • - Women with ongoing pregnancy or breast feeding
  • - Male partners of women who are pregnant

研究者

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