EUCTR2011-000945-19-EE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
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 10,470
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
- •1. Willing and able to provide written informed consent;
- •2. Have previously participated in a Gilead-sponsored hepatitis C study and received at least one Gilead OAV;
- •3. Have achieved SVR in a Gilead-sponsored study, as defined in the original treatment protocol;
- •4. 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 10000
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 470
排除标准
- •1. 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.
- •2. 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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