Safety and Pharmacokinetics of Glecaprevir/Pibrentasvir in Adults With Chronic Genotype 1–6 Hepatitis C Virus Infections and Compensated Liver Disease
Author(s) -
Edward Gane,
Fred Poordad,
Neddie Zadeikis,
Joaquin Valdes,
Chih-Wei Lin,
Wei Liu,
Armen Asatryan,
Stanley Wang,
Catherine Stedman,
Susan Greenbloom,
Tuan Nguyen,
Magdy Elkhashab,
MarcusAlexander Wörns,
Albert Tran,
Jean-Pierre Mulkay,
Carolyn M. Setze,
Yao Yu,
Edward Tam,
Ariel Porcalla,
Federico Mensa
Publication year - 2019
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1093/cid/ciz022
Subject(s) - genotype , pharmacokinetics , medicine , liver disease , hepatitis c virus , disease , virology , virus , gastroenterology , biology , genetics , gene
Untreated, chronic hepatitis C virus (HCV) infection may lead to progressive liver damage, which can be mitigated by successful treatment. This integrated analysis reports the safety, efficacy, and pharmacokinetics (PK) of the ribavirin-free, direct-acting, antiviral, fixed-dose combination of glecaprevir/pibrentasvir (G/P) in patients with chronic HCV genotype 1-6 infections and compensated liver disease, including patients with chronic kidney disease stages 4 or 5 (CKD 4/5).
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