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Efficacy and safety of danoprevir-ritonavir plus peginterferon alfa-2a-ribavirin in hepatitis C virus genotype 1 prior null responders

  • Edward J. Gane
  • , Régine Rouzier
  • , Alicja Wiercinska-Drapalo
  • , Dominique G. Larrey
  • , Peter N. Morcos
  • , Barbara J. Brennan
  • , Sophie Le Pogam
  • , Isabel Nájera
  • , Rosemary Petric
  • , Jonathan Q. Tran
  • , Rohit Kulkarni
  • , Ying Zhang
  • , Patrick Smith
  • , Ellen S. Yetzer
  • , Nancy S. Shulman
  • Auckland Clinical Studies
  • CAP Center
  • Medical University of Warsaw
  • CHU Montpellier
  • Hoffmann-La Roche Inc.
  • Celgene Corporation
  • Biogen IDEC
  • Genentech, Inc
  • Guardian Analytics
  • Yingstat Consulting LLC
  • AbbVie

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

Danoprevir (DNV) is a hepatitis C virus (HCV) protease inhibitor that achieves high sustained virologic response (SVR) rates in combination with peginterferon alfa-2a-ribavirin in treatment-naive HCV genotype 1 (G1)-infected patients. This study explored the efficacy and safety of ritonavir-boosted DNV (DNVr) plus peginterferon alfa-2a-ribavirin in G1-infected prior peginterferon- ribavirin null responders. Null responders (<2-log10 reduction in HCV RNA level at week 12) were given an open-label combination of 100 mg of ritonavir and 100 mg of DNV (100/100 mg DNVr) every 12 h (q12h) plus peginterferon alfa-2a-ribavirin for 12 weeks. All patients achieving an early virologic response (EVR;>2-log10 decrease in HCV RNA by week 12) continued treatment with peginterferon alfa-2a-ribavirin; those without an EVR discontinued all study drugs. Twenty-four prior null responders were enrolled; 16 patients (67%) were infected with HCV G1b, and 8 (33%) were infected with G1a. Ninety-six percent of patients had an IL28B non-CC genotype. A sustained virologic response at 24 weeks posttreatment (SVR24) was achieved in 67% of patients, with a higher rate in G1b-infected (88%) than G1a-infected (25%) patients. Resistance-related breakthrough occurred in 4/8 G1a and 1/16 G1b patients through the DNV resistance-associated variant (RAV) NS3 R155K. NS3 R155K was also detected in 2/2 G1a patients who relapsed. Treatment was well tolerated. Two patients withdrew prematurely from study medications due to adverse events. Two serious adverse events were reported; both occurred after completion of DNVr therapy and were considered unrelated to treatment. No grade 3 or 4 alanine aminotransferase (ALT) elevations were observed. DNVr plus peginterferon alfa-2a-ribavirin demonstrated high SVR24 rates in HCV G1b-infected prior null responders and was well tolerated. (This study has been registered at ClinicalTrials.gov under registration no. NCT01185860.).

Original languageEnglish
Pages (from-to)1136-1145
Number of pages10
JournalAntimicrobial Agents and Chemotherapy
Volume58
Issue number2
DOIs
StatePublished - Feb 2014

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