Faldaprevir for the treatment of genotype-1 hepatitis C virus

Expert Rev Gastroenterol Hepatol. 2015 Mar;9(3):277-88. doi: 10.1586/17474124.2015.1001742. Epub 2015 Jan 29.

Abstract

Historically, pegylated interferon in combination with ribavirin was the standard of care in hepatitis C virus; however, this combination is often poorly tolerated, has a significant side-effect profile and is of limited efficacy in hepatitis C virus genotype-1. More recently, pegylated interferon/ribavirin has been combined with direct acting antiviral agents such as the first generation NS3/4A protease inhibitors. Faldaprevir, a first generation, second-wave protease inhibitor, when used with a pegylated interferon/ribavirin regimen, has also been shown to increase treatmentsuccess while shortening treatment duration; however, second generation direct acting antiviral agents offer even betterefficacy and tolerability. Various direct acting antiviral agent combinations in interferon-free regimens have been effective in over 95% of patients and are now in licensed use. While faldaprevir was a pioneering drug, by the time it reached late phase development it was superseded by newer agents.

Keywords: boceprevir; faldaprevir; hepatitis C; liver transplantation; pegylated interferon; ribavirin; simeprevir; telaprevir.

Publication types

  • Review

MeSH terms

  • Aminoisobutyric Acids
  • Antiviral Agents / adverse effects
  • Antiviral Agents / therapeutic use*
  • Clinical Trials as Topic
  • Drug Therapy, Combination
  • Genotype
  • Hepacivirus / genetics*
  • Hepatitis C / drug therapy*
  • Hepatitis C / virology
  • Humans
  • Interferons / therapeutic use
  • Leucine / analogs & derivatives
  • Oligopeptides / adverse effects
  • Oligopeptides / therapeutic use*
  • Polyethylene Glycols / therapeutic use
  • Proline / analogs & derivatives
  • Protease Inhibitors / therapeutic use
  • Quinolines
  • Ribavirin / therapeutic use
  • Thiazoles / adverse effects
  • Thiazoles / therapeutic use*

Substances

  • Aminoisobutyric Acids
  • Antiviral Agents
  • Oligopeptides
  • Protease Inhibitors
  • Quinolines
  • Thiazoles
  • Polyethylene Glycols
  • Ribavirin
  • Interferons
  • faldaprevir
  • Proline
  • Leucine