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Dual daclatasvir and sofosbuvir for treatment of genotype 3 chronic hepatitis C virus infection

  • Vinay Sundaram
  • , Kris V. Kowdley

Research output: Contribution to journalReview articlepeer-review

12 Scopus citations

Abstract

Chronic hepatitis C virus (HCV) infection is one of the most common etiologies of liver-related mortality throughout the world. Traditionally, therapy has been focused on pegylated interferon in combination with ribavirin, with clinical trials demonstrating that HCV genotype 1 had the lowest response rate (40-50%), while genotype 3 had an intermediate response rate (60- 70%). Recently, significant advances have been made with all-oral direct-acting antiviral (DAA) therapy, which have significantly improved cure rates for HCV genotype 1. Accordingly, HCV genotype 3 is now potentially the most difficult to treat. One of the most potent DAA medications is sofosbuvir, a pan-genotypic nucleotide analogue that inhibits the NS5B polymerase of HCV. Daclatasvir, a pan-genotypic inhibitor of the HCV NS5A replication complex, was recently approved in the United States for treatment of HCV genotype 3 in conjunction with sofosbuvir. This combination may provide a powerful tool in the treatment of HCV genotype 3.

Original languageEnglish
Pages (from-to)13-20
Number of pages8
JournalExpert Review of Gastroenterology and Hepatology
Volume10
Issue number1
DOIs
StatePublished - Jan 1 2016

Keywords

  • Direct-acting antiviral
  • Genotype 1
  • Pegylated interferon
  • Ribavirin

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