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

Liver Int. 2014 Feb;34 Suppl 1(Suppl 1):69-78. doi: 10.1111/liv.12423.

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.

Keywords: asunaprevir; daclatasvir; faldaprevir; pegylated interferon; ribavirin; simeprevir; sofosbuvir.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Aminoisobutyric Acids
  • Antiviral Agents / pharmacology
  • Antiviral Agents / therapeutic use*
  • Carbamates
  • Clinical Trials as Topic
  • Disease Eradication / methods
  • Disease Eradication / trends*
  • Drug Discovery / methods*
  • Drug Therapy, Combination / methods*
  • Drug Therapy, Combination / trends
  • Hepacivirus / drug effects*
  • Hepacivirus / genetics
  • Hepatitis C / drug therapy*
  • Heterocyclic Compounds, 3-Ring
  • Humans
  • Imidazoles
  • Interferon-alpha
  • Isoquinolines
  • Leucine / analogs & derivatives
  • Oligopeptides
  • Polyethylene Glycols
  • Proline / analogs & derivatives
  • Protease Inhibitors / pharmacology
  • Pyrrolidines
  • Quinolines
  • Recombinant Proteins
  • Ribavirin
  • Simeprevir
  • Sofosbuvir
  • Sulfonamides
  • Thiazoles
  • Uridine Monophosphate / analogs & derivatives
  • Valine / analogs & derivatives
  • Viral Nonstructural Proteins / antagonists & inhibitors
  • Virus Replication / drug effects
  • Virus Replication / physiology*

Substances

  • Aminoisobutyric Acids
  • Antiviral Agents
  • Carbamates
  • Heterocyclic Compounds, 3-Ring
  • Imidazoles
  • Interferon-alpha
  • Isoquinolines
  • Oligopeptides
  • Protease Inhibitors
  • Pyrrolidines
  • Quinolines
  • Recombinant Proteins
  • Sulfonamides
  • Thiazoles
  • Viral Nonstructural Proteins
  • Polyethylene Glycols
  • Ribavirin
  • faldaprevir
  • Proline
  • Simeprevir
  • Uridine Monophosphate
  • NS-5 protein, hepatitis C virus
  • Leucine
  • Valine
  • daclatasvir
  • peginterferon alfa-2a
  • asunaprevir
  • Sofosbuvir