| Literature DB >> 30499343 |
Federico J Mensa1, Sandra Lovell2, Tami Pilot-Matias3, Wei Liu4.
Abstract
In recent years, management of chronic hepatitis C virus (HCV) infection has been revolutionized by the availability of oral direct-acting antivirals (DAAs), which have significantly better efficacy and safety profiles than interferon-containing regimens. Simple, short-duration DAA therapies will facilitate expansion of HCV treatment to nonspecialist providers, which will be vital to achieve the WHO target of eliminating chronic HCV as a major public health threat by 2030. Coformulated glecaprevir/pibrentasvir is the only 8-week, pan-genotypic, 2-DAA regimen recommended by international guidelines as a first-line regimen in treatment-naive, noncirrhotic HCV genotype 1-6 patients. This review provides a comprehensive summary of the pharmacodynamic and pharmacokinetic parameters, efficacy, safety and place in the HCV treatment paradigm for glecaprevir/pibrentasvir.Entities:
Keywords: HCV; HIV; NS3/4A protease inhibitor; NS5A inhibitor; chronic HCV infection; chronic kidney disease; cirrhosis; glecaprevir; hepatitis C virus; pibrentasvir
Mesh:
Substances:
Year: 2018 PMID: 30499343 DOI: 10.2217/fmb-2018-0233
Source DB: PubMed Journal: Future Microbiol ISSN: 1746-0913 Impact factor: 3.165