EUCTR2011-006132-24-ES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 Farmaceutica, S.A.0 个研究点目标入组 650 人开始时间: 2012年4月12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）
- 发起方
- 入组人数
- 650
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 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
- •F.1.3.1 Number of subjects for this age range 65
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
研究者
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