Directly acting antivirals for the treatment of patients with hepatitis C infection: a clinical development update addressing key future challenges.

Published

Journal Article (Review)

Current therapy for chronic hepatitis C virus (HCV) infection is effective in less than 50% of genotype 1-infected patients. Antiviral agents specifically targeting either the HCV protease or polymerase, or other targets, are now in clinical development. In general, direct antivirals are potent inhibitors of HCV replication and can result in rapid declines in serum HCV RNA levels. Yet these agents drive selection pressure for mutant viruses that can reduce susceptibility to any given drug. Using pegylated interferon (PEG-IFN) and ribavirin (RBV) in combination with direct antivirals can suppress viral breakthrough and increase the likelihood of sustained virologic response. Direct antivirals also result in adverse events in a proportion of patients, adding to concerns of tolerability that exist with PEG-IFN and RBV. Direct antivirals are very likely to become an integral part of treatment within the next decade, and already their use in clinical trials has raised important issues related to duration of treatment, early stopping rules, retreatment of previously treated patients, and how or when direct antivirals should be combined. Here, we provide current information regarding the effectiveness of direct antivirals in treating chronic HCV infection and discuss the key questions and challenges now facing the field.

Full Text

Duke Authors

Cited Authors

  • Thompson, A; Patel, K; Tillman, H; McHutchison, JG

Published Date

  • January 2009

Published In

Volume / Issue

  • 50 / 1

Start / End Page

  • 184 - 194

PubMed ID

  • 19022518

Pubmed Central ID

  • 19022518

International Standard Serial Number (ISSN)

  • 0168-8278

Digital Object Identifier (DOI)

  • 10.1016/j.jhep.2008.10.011

Language

  • eng

Conference Location

  • Netherlands