EUCTR2011-000945-19-IT进行中（未招募）1 期
A long term follow-up registry for subjects who achieve a sustained virologic response to treatment in Gilead Sponsored Trials in subjects with chronic hepatitis C infection
GILEAD SCIENCE INC.0 个研究点目标入组 740 人开始时间: 2012年3月8日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 740
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
- •Willing and able to provide written informed consent; Have previously participated in a Gilead-sponsored hepatitis C study and received at least one Gilead OAV; Have achieved SVR in a Gilead-sponsored study, as defined in the original treatment protocol; Be willing and able to comply with the visit schedule and protocol-mandated procedures.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 666
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 74
排除标准
- •Subject plans to start a new course of hepatitis C therapy including any investigational drug or device during the course of the follow-up Registry. History of clinically-significant illness or any other major medical disorder that may interfere with subject follow-up, assessments or compliance with the protocol.
研究者
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