跳至主要内容
临床试验/EUCTR2011-006132-24-HU
EUCTR2011-006132-24-HU
进行中(未招募)
不适用

A multi-centre 3-year follow-up study to assess the viral activity in patients who failed to achieve sustained virologic response in Novartis-sponsored alisporivir studies for chronic hepatitis C patients

ovartis Pharma Services AG0 个研究点目标入组 650 人2012年4月17日

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
未指定
发起方
ovartis Pharma Services AG
入组人数
650
状态
进行中(未招募)
最后更新
12年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2012年4月17日
结束日期
待定
最后更新
12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

  • \-Written informed consent must be obtained before any assessment is performed
  • \-Males or females aged 18 or greater
  • \-Have previously completed a Novartis\-sponsored hepatitis C study and received alisporivir or a direct antiviral agent
  • \-Have not acheived SVR24
  • \-Be 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 650
  • F.1\.3 Elderly (\>\=65 years) yes

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
  • \-Previous use of any course of hepatitis C therapy since the end of the Novartis\-sponsored hepatitis C study

结局指标

主要结局

未指定

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