Viral kinetics in patients with chronic hepatitis C treated with the serine protease inhibitor BILN 2061

Antivir Ther. 2006;11(3):371-6.

Abstract

We analysed viral kinetics from a 2-day treatment with BILN 2061, a serine protease inhibitor of hepatitis C virus, in patients chronically infected with genotype 1 hepatitis C virus. The efficiency (E), describing inhibition of viral production, was above 99.45% in all patients with minor or moderate fibrosis receiving doses of 200mg and 500 mg twice daily and larger than in previous studies for interferon-based treatments. However, epsilon was slightly smaller in patients with cirrhosis given 200mg and markedly smaller in patients given 25 mg. Estimates of viral clearance and infected-cell loss support conclusions on these rates and on treatment mechanisms from previous studies on interferon-alpha-based treatments.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antiviral Agents / therapeutic use
  • Area Under Curve
  • Carbamates / administration & dosage
  • Carbamates / pharmacokinetics
  • Carbamates / therapeutic use*
  • Female
  • Hepacivirus / drug effects*
  • Hepatitis C, Chronic / drug therapy*
  • Hepatitis C, Chronic / virology
  • Humans
  • Interferon-alpha / therapeutic use
  • Kinetics
  • Macrocyclic Compounds / administration & dosage
  • Macrocyclic Compounds / pharmacokinetics
  • Macrocyclic Compounds / therapeutic use*
  • Male
  • Middle Aged
  • Models, Biological
  • Quinolines / administration & dosage
  • Quinolines / pharmacokinetics
  • Quinolines / therapeutic use*
  • RNA, Viral / blood*
  • Serine Proteinase Inhibitors / administration & dosage
  • Serine Proteinase Inhibitors / pharmacokinetics
  • Serine Proteinase Inhibitors / therapeutic use*
  • Thiazoles / administration & dosage
  • Thiazoles / pharmacokinetics
  • Thiazoles / therapeutic use*

Substances

  • Antiviral Agents
  • BILN 2061
  • Carbamates
  • Interferon-alpha
  • Macrocyclic Compounds
  • Quinolines
  • RNA, Viral
  • Serine Proteinase Inhibitors
  • Thiazoles