跳至主要内容
临床试验/EUCTR2011-006131-38-GB
EUCTR2011-006131-38-GB进行中(未招募)不适用

A multi-centre 3-year follow-up study to assess the durability of sustained virologic response in alisporivir treated chronic hepatitis C patients - NA

ovartis Pharma Services AG0 个研究点目标入组 2,000 人开始时间: 2012年5月10日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
2,000

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

  • -Written informed consent must be obtained before any assessment is performed
  • -Males or females must be aged 18 years or older
  • -Have previously completed a Novartis-sponsored hepatitis C study and received alisporivir
  • -Have achieved SVR24
  • -Are able to comply with visit schedule
  • 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 2000
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • -Use of any investigational drugs within 5 half-lives of enrollment, or within 30 days of that medication, whichever is longer
  • -Use or planned use to start a new course of hepatitis C therapy

研究者

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