Abstract
In 247 subjects with hepatitis C virus genotype 1 infection treated with the interferon-free regimen of ABT-450/ritonavir, ombitasvir, and dasabuvir plus ribavirin, concordance of a sustained virologic response at 12 and 24 weeks supports the use of the earlier time point as a primary efficacy endpoint for trials of this interferon-free regimen.
Keywords:
concordance; direct-acting antivirals; hepatitis C; sustained virologic response.
© The Author 2014. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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2-Naphthylamine
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Adult
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Anilides / therapeutic use*
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Antiviral Agents / therapeutic use
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Carbamates / therapeutic use*
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Cyclopropanes
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Drug Resistance, Viral / genetics
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Drug Therapy, Combination
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Genotype
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Hepacivirus / drug effects*
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Hepacivirus / genetics
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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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Interferons
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Lactams, Macrocyclic
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Macrocyclic Compounds / therapeutic use*
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Male
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Proline / analogs & derivatives
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RNA, Viral / genetics
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Recurrence
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Ribavirin / therapeutic use*
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Ritonavir / therapeutic use*
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Sulfonamides / therapeutic use*
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Uracil / analogs & derivatives*
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Uracil / therapeutic use
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Valine
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Viral Load
Substances
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Anilides
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Antiviral Agents
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Carbamates
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Cyclopropanes
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Lactams, Macrocyclic
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Macrocyclic Compounds
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RNA, Viral
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Sulfonamides
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ombitasvir
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Ribavirin
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Uracil
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Interferons
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Proline
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2-Naphthylamine
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dasabuvir
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Valine
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Ritonavir
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paritaprevir