The NS5A replication complex inhibitor, BMS-790052, inhibits hepatitis C virus (HCV) replication with picomolar potency in preclinical assays. This potency translated in vivo to a substantial antiviral effect in a single-ascending dose study and a 14-day multiple-ascending dose (MAD) monotherapy stu
Multiple ascending dose study of BMS-790052, a nonstructural protein 5A replication complex inhibitor, in patients infected with hepatitis C virus genotype 1
โ Scribed by Richard E. Nettles; Min Gao; Marc Bifano; Ellen Chung; Anna Persson; Thomas C. Marbury; Ronald Goldwater; Michael P. DeMicco; Maribel Rodriguez-Torres; Apinya Vutikullird; Ernesto Fuentes; Eric Lawitz; Juan Carlos Lopez-Talavera; Dennis M. Grasela
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 282 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0270-9139
No coin nor oath required. For personal study only.
โฆ Synopsis
Abbreviations: AE, adverse event; AUC, area under the plasma concentration time curve; AUC (TAU) , AUC over 12-hour dosing interval for 30 mg twice daily; C min , minimum observed plasma concentration; C max , maximum observed plasma concentration; C trough , trough concentrations; CLT/F, apparent total body clearance; CV, coefficient of variation; DAA, direct-acting antiviral; ECG, electrocardiogram; HCV, hepatitis C virus; ISG, interferon-stimulated gene; NS5A, nonstructural protein 5A; PCR, polymerase chain reaction; PEG-IFN, pegylated interferon; PK, pharmacokinetics; daily; RBV, ribavirin; T max , time of maximum observed plasma concentration; T 1/2 , half life.
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