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      HCV direct-acting antiviral agents: the best interferon-free combinations

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          Abstract

          For HCV infection, there have been major advancements during last several years with large numbers of ongoing trials with various direct-acting antivirals (DAA) showing high potency, favourable tolerability profile, higher barrier to resistance, shortened treatment duration, all oral regimen, pangenotypic, fewer drug interactions and reduced pill burden. By 2014, several DAAs are anticipated to complete successful phase III trials and will be commercially available. Initially, a wave of IFN-based regimen (sofosbuvir, faldaprevir and simeprevir) will be available for treatment of HCV genotype 1. In the near future, combination of antiviral agents with additive potency that lack cross-resistance with good safety profile will likely be the new recommended regimens, making HCV, the first chronic viral infection to be eradicated worldwide with a finite duration of combination DAA therapy without IFN or ribavirin. The aim of this review was to summarize the results obtained from recent DAA combination studies without IFN.

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          Author and article information

          Journal
          101160857
          30291
          Liver Int
          Liver Int
          Liver international : official journal of the International Association for the Study of the Liver
          1478-3223
          1478-3231
          8 December 2020
          February 2014
          15 December 2020
          : 34
          : Suppl 1
          : 69-78
          Affiliations
          [1 ]Center for AIDS Research, Emory University School of Medicine and Veterans Affairs Medical Center, Decatur, GA, USA
          [2 ]Internal Medicine and Infectious Diseases Department, Hôpital Europeen and Laboratoire Alphabio Marseille, Marseille, France
          [3 ]Hepatology Department, AP-HP, University Paris Diderot 7 and INSERM U773, CRB3, Beaujon Hospital, Clichy, France
          Author notes
          Correspondence: Raymond F. Schinazi, PhD, DSc, Center for AIDS Research, Emory University School of Medicine and Veterans Affairs Medical Center, Decatur, Georgia 30033, USA, Tel: +1 404 727 1414, Fax: +1 404 727 1330, rschina@ 123456emory.edu , (or), Tarik Asselah, MD, PhD, Hepatology, Department, AP-HP, University Paris Diderot, 7 and INSERM U773, CRB3, Beaujon Hospital, 100 Bd du Général Leclerc, Clichy 92110, France, Tel: +33(0) 140875579, Fax: +33(0) 147309440, tarik.asselah@ 123456bjn.aphp.fr
          Article
          PMC7737539 PMC7737539 7737539 nihpa1652791
          10.1111/liv.12423
          7737539
          24373081
          87948b36-4d01-4c29-b028-2129672e4396
          History
          Categories
          Article

          simeprevir,asunaprevir,pegylated interferon,ribavirin,faldaprevir,sofosbuvir,daclatasvir

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