Expert Opinion on Pharmacotherapy · 2015 · 33 citations · 15 references
MedicinePharmacologyPharmacotherapyMolecular PharmacologyMolecular VirologyVirologyAntiviral AgentsAntiviral PharmacologyAntiviral PharmacotherapyAntiviral TherapyViral HepatitisViral Hepatitis TreatmentAntiviral TherapeuticsDirect-acting Antiviral AgentsDirect-acting AntiviralsNon-nucleoside AntiviralsNon-nucleoside InhibitorsNucleoside AnalogsRna-dependent Rna Polymerase FunctionViral Rna Synthesis
INTRODUCTION: Treatment of hepatitis C virus (HCV) infection with direct-acting antivirals (DAAs) has revolutionized the care of infected patients. Among these novel compounds are non-nucleoside analogs, which bind viral RNA-dependent RNA polymerase resulting in a conformational change inhibiting RNA synthesis. AREAS COVERED: Efficacy and tolerability of treatment regimens containing the non-nucleoside analog polymerase inhibitor dasabuvir (ABT-333). EXPERT OPINION: Dasabuvir-containing regimens achieve high rates of sustained virologic response in HCV genotype 1a and 1b-infected patients when combined with other DAAs, namely paritaprevir (ABT-450), ritonavir and ombitasvir (ABT-267). In the populations studied, dasabuvir seems to be well tolerated and safe. The major limitations of this novel drug are its genotype-restricted activity, the necessity to include ribavirin for HCV genotype 1a and the emergence of resistance if not combined with other DDAs.
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Evolving epidemiology of hepatitis C virus
Daniel Lavanchy · Clinical Microbiology and Infection · 2010 · 1.3K citations · Full text
ABT-450/r–Ombitasvir and Dasabuvir with or without Ribavirin for HCV
Péter Ferenci, David Bernstein, Jacob Lalezari et al. · New England Journal of Medicine · 2014 · 695 citations · Full text