跳至主要内容
临床试验/EUCTR2011-001878-25-BG
EUCTR2011-001878-25-BG进行中(未招募)不适用

A Randomized, Double-Blind Study to Evaluate the Safety and Antiviral Activity of IDX184 in Combination with Pegylated Interferon and Ribavirin for 12 Weeks in Treatment-Naïve Subjects with Genotype 1 Chronic Hepatitis C Infection

Idenix Pharmaceuticals, Inc.0 个研究点目标入组 100 人开始时间: 2011年11月9日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
100

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

  • Males and females with documented genotype 1, chronic hepatitis C infection.
  • Subjects must agree to use double-barrier method of birth control for at least 6 months after the last dose of study drugs.
  • Written informed consent by subject.
  • 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 100
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Prior HCV treatment.
  • Pregnant or breastfeeding.
  • Co-infected with hepatitis B virus (HBV; hepatitis B surface antigen (HBsAg) positive) and/or human immunodeficiency virus (HIV).

研究者

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