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
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Clinical Trial
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Antiviral Agents / therapeutic use
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Area Under Curve
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Carbamates / administration & dosage
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Carbamates / pharmacokinetics
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Carbamates / therapeutic use*
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Female
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Hepacivirus / drug effects*
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Hepatitis C, Chronic / drug therapy*
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Hepatitis C, Chronic / virology
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Humans
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Interferon-alpha / therapeutic use
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Kinetics
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Macrocyclic Compounds / administration & dosage
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Macrocyclic Compounds / pharmacokinetics
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Macrocyclic Compounds / therapeutic use*
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Male
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Middle Aged
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Models, Biological
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Quinolines / administration & dosage
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Quinolines / pharmacokinetics
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Quinolines / therapeutic use*
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RNA, Viral / blood*
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Serine Proteinase Inhibitors / administration & dosage
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Serine Proteinase Inhibitors / pharmacokinetics
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Serine Proteinase Inhibitors / therapeutic use*
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Thiazoles / administration & dosage
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Thiazoles / pharmacokinetics
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Thiazoles / therapeutic use*
Substances
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Antiviral Agents
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BILN 2061
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Carbamates
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Interferon-alpha
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Macrocyclic Compounds
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Quinolines
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RNA, Viral
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Serine Proteinase Inhibitors
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Thiazoles