Simeprevir: A macrocyclic hcv protease inhibitor

R. Talwani, E. L. Heil, B. L. Gilliam, Zelalem Temesgen

Research output: Contribution to journalReview article

18 Scopus citations

Abstract

Simeprevir is a macrocyclic NS3/4A HCV protease inhibitor with potent activity against genotypes 1, 2, 4, 5 and 6 of the hepatitis C virus (HCV). Phase II and III studies of simeprevir combined with pegylated interferon (peg-IFN) and ribavirin (RBV) demonstrated that the combination was safe and effective in HCV genotype 1 patients, with more than 75% of treatment-naive patients attaining a sustained virological response (SVR). Simeprevir is administered once daily as a single 150-mg capsule. It has a moderate drug interaction potential, but less than that of the first-generation HCV protease inhibitors. Based on positive results from the product's phase III clinical program, simeprevir was approved and launched in Japan, the U.S. and Canada in late 2013 for use in combination with peg-IFN/RBV in HCV genotype 1 infections. Phase II interferon-free studies of simeprevir are ongoing.

Original languageEnglish (US)
Pages (from-to)769-779
Number of pages11
JournalDrugs of Today
Volume49
Issue number12
DOIs
StatePublished - Dec 1 2013

Keywords

  • GT-1
  • Hepatitis C virus
  • Macrolide
  • Simeprevir
  • TMC-435

ASJC Scopus subject areas

  • Pharmacology
  • Pharmacology (medical)

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