EUCTR2006-006529-25-PT进行中（未招募）不适用
ong-Term Follow-Up of Subjects in a Phase 1, 2, or 3 CLinical Trial in Which Boceprevir or Narlaprevir was Administered for the Treatment of Chronic Hepatitis C
Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.0 个研究点目标入组 2,800 人开始时间: 2010年11月22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
- 2,800
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
- •-Subject must be willing to give written informed consent.
- •-Subject must have received at least one dose of any study medication
- •(peginterferon, ribavirin, boceprevir or narlaprevir) in a previous SPRI Phase
- •1, 2, or 3 clinical study in which boceprevir or narlaprevir was administered.
- •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
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •-Concurrent participation in any other clinical study for the treatment of chronic
- •hepatitis C.
- •-Retreatment with any antiviral or immunomodulatory drug for chronic hepatitis C
- •after completion of, or discontinuation from, the SPRI Phase 1, 2, or 3 clinical
- •study in which the subject previously participated.
- •-Any condition which in the opinion of the Investigator would make the subject
- •unsuitable for enrollment.
研究者
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