Publication

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

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Last modified
  • 05/22/2025
Type of Material
Authors
    Raymond Schinazi, Emory UniversityPhilippe Halfon, Hôpital Europeen and Laboratoire Alphabio MarseillePatrick Marcellin, University Paris Diderot 7 and INSERM U773Tarik Asselah, University Paris Diderot 7 and INSERM U773
Language
  • English
Date
  • 2014-02-01
Publisher
  • WILEY
Publication Version
Copyright Statement
  • 2014
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 34
Issue
  • SUPPL1
Start Page
  • 69
End Page
  • 78
Grant/Funding Information
  • This work was supported in part by CFAR NIH grant 2P30AI-050409 (to RFS) and by the Department of Veterans Affairs (to RFS). We thank Judy Mathew and Steve Coats for proofing this manuscript. Dr. Schinazi is the founder and a major shareholder of RFS Pharma, LLC.
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, pan-genotypic, 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. © 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
Author Notes
  • Raymond F. Schinazi, PhD, DSc.
Keywords
Research Categories
  • Health Sciences, General
  • Engineering, Biomedical

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