Faldaprevir for the treatment of hepatitis C

Drugs Today (Barc). 2015 May;51(5):289-301. doi: 10.1358/dot.2015.51.5.2321008.

Abstract

Enormous progress has been made in the understanding of the hepatitis C virus and the development of novel therapeutic agents since the identification of the virus, from initial interferon monotherapy to PEGylated interferon in combination with ribavirin for 48-72 weeks that used to be the standard of care in hepatitis C virus therapy. However, this combination has limited efficacy and a significant side effect profile including flu-like symptoms, anemia, leukopenia, autoimmune disorders and depression, so it is often poorly tolerated. Recently, direct-acting antiviral agents, such as the first-generation NS3/4A protease inhibitors, have been added to this combination, improving the percentage of successful treatments. Faldaprevir is a first-generation, second wave, protease inhibitor that, when combined with PEGylated interferon and ribavirin, has been shown to increase treatment success with shorter treatment duration. Various direct-acting antiviral agent combinations in interferon-free regimens have been effective in over 95% of patients and are now in licensed use.

Keywords: BI-201335; Faldaprevir; HCV NS3 NS4A protease inhibitors; PEGylated interferon; Ribavirin.

Publication types

  • Review

MeSH terms

  • Aminoisobutyric Acids
  • Animals
  • Antiviral Agents / administration & dosage
  • Antiviral Agents / adverse effects
  • Antiviral Agents / pharmacokinetics
  • Antiviral Agents / therapeutic use*
  • Clinical Trials as Topic
  • Dose-Response Relationship, Drug
  • Drug Discovery*
  • Drug Interactions
  • Hepatitis C / drug therapy*
  • Humans
  • Leucine / analogs & derivatives
  • Molecular Structure
  • Oligopeptides / administration & dosage
  • Oligopeptides / adverse effects
  • Oligopeptides / pharmacokinetics
  • Oligopeptides / therapeutic use*
  • Proline / analogs & derivatives
  • Quinolines
  • Thiazoles / administration & dosage
  • Thiazoles / adverse effects
  • Thiazoles / pharmacokinetics
  • Thiazoles / therapeutic use*
  • Tissue Distribution
  • Treatment Outcome
  • Viral Nonstructural Proteins / antagonists & inhibitors*

Substances

  • Aminoisobutyric Acids
  • Antiviral Agents
  • NS3 protein, hepatitis C virus
  • Oligopeptides
  • Quinolines
  • Thiazoles
  • Viral Nonstructural Proteins
  • faldaprevir
  • Proline
  • Leucine