Abstract | INTRODUCTION: Hepatitis C virus (HCV) therapy continues to evolve rapidly. ABT-450 is a novel potent inhibitor of the non-structural 3/4A protease that has been studied in combination with several agents, allowing shorter duration of therapy and interferon-free/ ribavirin-free all-oral regimens. Preliminary data from studies evaluating these new regimens are impressive with sustained virological response (SVR) rates of 88 - 100% after 12 weeks of therapy in patients with previously untreated HCV genotype 1 infection. SVR rates in treatment-experienced patients are also encouraging. AREAS COVERED: Efficacy and tolerability of antiviral regimens containing ABT-450 boosted with ritonavir ( ABT-450/r). Results from published studies and abstracts from recent meetings are presented. EXPERT OPINION:
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Authors | Andres F Carrion, Julio Gutierrez, Paul Martin |
Journal | Expert opinion on pharmacotherapy
(Expert Opin Pharmacother)
Vol. 15
Issue 5
Pg. 711-6
(Apr 2014)
ISSN: 1744-7666 [Electronic] England |
PMID | 24517400
(Publication Type: Journal Article, Review)
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Chemical References |
- Antiviral Agents
- Cyclopropanes
- Lactams, Macrocyclic
- Macrocyclic Compounds
- NS3 protein, hepatitis C virus
- Sulfonamides
- Viral Nonstructural Proteins
- Ribavirin
- Proline
- Ritonavir
- paritaprevir
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Topics |
- Antiviral Agents
(therapeutic use)
- Cyclopropanes
- Drug Therapy, Combination
- Genotype
- Hepacivirus
(drug effects, genetics)
- Hepatitis C
(drug therapy)
- Hepatitis C, Chronic
(drug therapy)
- Humans
- Lactams, Macrocyclic
- Macrocyclic Compounds
(therapeutic use)
- Proline
(analogs & derivatives)
- Ribavirin
(therapeutic use)
- Ritonavir
(therapeutic use)
- Sulfonamides
- Viral Nonstructural Proteins
(antagonists & inhibitors)
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