A phase 2B study of MK-7009 (vaniprevir) in patients with genotype 1 HCV infection who have failed previous pegylated interferon and ribavirin treatment

Eric Lawitz, Maribel Rodriguez-Torres, Albrecht Stoehr, Edward J. Gane, Lawrence Serfaty, Sanhita Bhanja, Richard J. Barnard, Di An, Jacqueline Gress, Peggy Hwang, Niloufar Mobashery

Research output: Contribution to journalArticlepeer-review

29 Scopus citations

Abstract

Background & Aims: MK-7009 (vaniprevir) is a non-covalent competitive inhibitor of the hepatitis C virus (HCV) NS3/4A protease. This report presents the primary analysis results (safety and sustained viral response) of a phase 2b study of MK-7009 given in combination with peginterferon (PegIFN) alfa2a 180 μg weekly and ribavirin (RBV) 1000-1200 mg/day, for 24-48 weeks to non-cirrhotic patients who have failed previous PegIFN and RBV treatment. Methods: We present results of a randomized, placebo-controlled, double-blind study of MK-7009 administered for 24-48 weeks in combination with PegIFN and RBV in 4 regimens to at least 40 patients per arm. Stratification by prior response to PegIFN and RBV was as follows: null response, partial response, breakthrough and relapse. HCV RNA was determined by Roche Cobas Taqman with a lower limit of detection (LLoD) of 10 IU/ml and a lower limit of quantification (LLoQ) of 25 IU/ml. Results: SVR24 in patients on MK-7009 + PegIFN and ribavirin (P/R) was statistically superior to placebo + P/R in all treatment groups (p <0.001). MK-7009 at 300 mg b.i.d. and 600 mg b.i.d. is generally well tolerated for use for up to 48 weeks of therapy. Patients in MK-7009 regimens had higher rates of gastrointestinal adverse events as compared to control (mostly mild to moderate). There were no significant differences in rates of anemia and rash between the MK-7009 regimens and control. Conclusions: In conclusion, patients treated with MK-7009 plus P/R experienced significant improvement in SVR compared to P/R control in a population of GT 1 experienced patients.

Original languageEnglish (US)
Pages (from-to)11-17
Number of pages7
JournalJournal of Hepatology
Volume59
Issue number1
DOIs
StatePublished - Jul 1 2013
Externally publishedYes

Keywords

  • Direct-acting antivirals
  • HCV
  • Vaniprevir

ASJC Scopus subject areas

  • Hepatology

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