Ontology highlight
ABSTRACT: Background
In study TMC647055HPC2001, a 3-direct-acting-antiviral (DAA) regimen combining NS3/4A protease inhibitor simeprevir (SMV), non-nucleoside NS5B inhibitor TMC647055/ritonavir (RTV) and NS5A inhibitor JNJ-56914845 resulted in high sustained virologic response 12 weeks after actual end of treatment (SVR12) in chronic hepatitis C virus (HCV) genotype 1-infected patients. SVR12 rates were generally lower in the 2-DAA regimen SMV + TMC647055/RTV with or without ribavirin. The objective of this study was to identify and characterise pre-existing and emerging resistance-associated variants (RAVs) in patients enrolled in study TMC647055HPC2001.Methods
HCV population sequencing analyses were performed on baseline isolates from all patients (n = 90) and post-baseline isolate
SUBMITTER: Vijgen L
PROVIDER: S-EPMC5452362 | biostudies-literature | 2017 May
REPOSITORIES: biostudies-literature