Glecaprevir + pibrentasvir (ABT493 + ABT-530) for the treatment of Hepatitis C

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

Introduction: Glecaprevir (formerly ABT-493, pangenotypic NS3/4A protease inhibitor) and pibrentasvir (formerly ABT-530, pangenotypic NS5A inhibitor) are second generation direct acting antivirals (DAA) for the treatment of chronic Hepatitis C (HCV). It is a fixed dose ribavirin (RBV)-free regimen with activity against genotypes (GT) 1–6. In vitro the two antivirals have synergistic activity with a high barrier to resistance and potent activity against common polymorphisms. It is once daily oral dosing with minimal absorption, primary biliary excretion, and negligible renal excretion, making it safe for patients with renal impairment. This regimen is being reviewed because it is the first pangenotypic regimen suitable for those with renal impairment and prior DAA failure. Areas covered: The key phase 2 and 3 trials which investigated the efficacy and safety of glecaprevir/pibrentasvir are reviewed by methodology, primary end point, baseline demographic data, response rates, and adverse events. Literature search methodology involved reviewing key abstracts presented at the American Association for the Study of Liver Disease and European Association for the Study of Liver. Expert commentary: The advantages and limitations of glecaprevir/pibrentasvir will be reviewed in comparison to its competitor drug on the market.

Original languageEnglish (US)
Pages (from-to)9-17
Number of pages9
JournalExpert Review of Gastroenterology and Hepatology
Volume12
Issue number1
DOIs
StatePublished - Jan 2 2018

Keywords

  • Chronic Hepatitis C
  • direct acting antivirals
  • glecaprevir/pibrentasvir
  • renal impairment sustained virologic response

ASJC Scopus subject areas

  • Hepatology
  • Gastroenterology

Fingerprint Dive into the research topics of 'Glecaprevir + pibrentasvir (ABT493 + ABT-530) for the treatment of Hepatitis C'. Together they form a unique fingerprint.

Cite this