EUCTR2010-019584-10-GB进行中（未招募）不适用
A Randomized, Open label, Multicenter, Dose and DurationFinding Study to Evaluate the Sustained Virologic Response ofthe HCV Protease Inhibitor Danoprevir (RO5190591) Boostedwith Low Dose Ritonavir (danoprevir/r) in Combination withPegasys® and Copegus® versus Pegasys® and Copegus® alonein Treatment-Naive Patients with Chronic Hepatitis C Genotype1 or 4 Virus Infection.
F.Hoffmann-La Roche0 个研究点目标入组 405 人开始时间: 2010年8月27日最近更新:
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
- 405
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
- •- Adults patients, >/=18 years of age
- •- Chronic Hepatitis C, Genotype 1 and 4
- •- HCV RNA >/=50,000 IU/mL
- •- treatment-naive
- •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 380
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 25
排除标准
- •- Patients with cirrhosis or incomplete/transition to cirrhosis
- •- Patients with other forms of liver disease, HIV infection, hepatocellular carcinoma or severe cardiac disease
研究者
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