Glecaprevir/pibrentasvir for the treatment of chronic hepatitis C virus infection

被引:12
|
作者
Mensa, Federico J. [1 ]
Lovell, Sandra [2 ]
Pilot-Matias, Tami [3 ]
Liu, Wei [4 ]
机构
[1] AbbVie Inc, Dept Clin Dev Infect Dis, N Chicago, IL 60064 USA
[2] AbbVie Inc, Dept Stat, N Chicago, IL 60064 USA
[3] AbbVie Inc, Dept Clin Virol, N Chicago, IL 60064 USA
[4] AbbVie Inc, Dept Pharmacokinet, N Chicago, IL 60064 USA
关键词
chronic HCV infection; chronic kidney disease; cirrhosis; glecaprevir; HCV; hepatitis C virus; HIV; NS3; 4A protease inhibitor; NS5A inhibitor; pibrentasvir; HCV GENOTYPE 1; COMPENSATED CIRRHOSIS; RESISTANCE ANALYSIS; NEXT-GENERATION; SAFETY; EFFICACY; PIBRENTASVIR; PHARMACOKINETICS; GLECAPREVIR; ADULTS;
D O I
10.2217/fmb-2018-0233
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:89 / 110
页数:22
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