首页> 外文期刊>The Lancet >Efficacy and safety of 12 weeks versus 18 weeks of treatment with grazoprevir (MK-5172) and elbasvir (MK-8742) with or without ribavirin for hepatitis C virus genotype 1 infection in previously untreated patients with cirrhosis and patients with previous null response with or without cirrhosis (C-WORTHY): a randomised, open-label phase 2 trial
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Efficacy and safety of 12 weeks versus 18 weeks of treatment with grazoprevir (MK-5172) and elbasvir (MK-8742) with or without ribavirin for hepatitis C virus genotype 1 infection in previously untreated patients with cirrhosis and patients with previous null response with or without cirrhosis (C-WORTHY): a randomised, open-label phase 2 trial

机译:接受或未接受利巴韦林的格拉佐普韦(MK-5172)和依巴斯韦(MK-8742)治疗丙型肝炎病毒基因型1感染的12周和18周治疗对以前未经治疗的肝硬化患者和既往有或没有治疗无效的患者的疗效和安全性无肝硬化(C-WORTHY):一项随机,开放标签的2期临床试验

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摘要

Background There is a high medical need for an interferon-free, all-oral, short-duration therapy for hepatitis C virus (HCV) that is highly effective across diverse patient populations, including patients with cirrhosis or previous null response to pegylated interferon (peginterferon) plus ribavirin (PR-null responders). We aimed to assess the efficacy, safety, and effective treatment duration of grazoprevir (an HCV NS3/4A protease inhibitor) combined with elbasvir (an HCV NS5A inhibitor) with or without ribavirin in patients with HCV genotype 1 infection with baseline characteristics of poor response.
机译:背景技术迫切需要针对丙型肝炎病毒(HCV)的无干扰素,全口服,短期治疗,这种疗法在包括肝硬化患者或以前对聚乙二醇干扰素(peginterferon)无效的患者中有效)和利巴韦林(PR无效反应者)。我们的目的是评估格拉佐普韦(一种HCV NS3 / 4A蛋白酶抑制剂)联合elbasvir(一种HCV NS5A抑制剂)联合或不联合利巴韦林在有HCV基因型1型感染且基线反应较差的患者中的疗效,安全性和有效治疗时间。

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