GRAZOPREVIR POTASSIUM HCV NS3 NS4A protease inhibitor Anti-hepatitis C virus drug

被引:2
作者
Majumdar, A.
Gilliam, B. L. [1 ]
机构
[1] Univ Maryland, Sch Med, Inst Human Virol, 725 West Lombard St, Baltimore, MD 21201 USA
关键词
Grazoprevir; MK-5172; Hepatitis C virus; Macrocyclic protease inhibitor; HEPATITIS-C VIRUS; TREATMENT-NAIVE PATIENTS; GENOTYPE; INFECTION; PROTEASE INHIBITOR; ELBASVIR MK-8742; NS3/4A PROTEASE; COMBINATION THERAPY; MK-5172; RIBAVIRIN; EFFICACY;
D O I
10.1358/dof.2016.041.02.2382555
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Grazoprevir is a second-generation macrocyclic NS3/NS4A hepatitis C virus (HCV) protease inhibitor with broad activity across multiple genotypes of the HCV. Results of phase II and III studies have been promising across various patient populations, including HIV/HCV coinfected patients, patients with and without cirrhosis who have failed prior therapy, and patients with chronic kidney disease. Grazoprevir is administered once daily as a 100-mg dose and will be available as a fixed-dose combination with elbasvir 50 mg. This review outlines in vivo and in vitro studies, pharmacodynamics and safety, and relevant clinical studies for this promising drug.
引用
收藏
页码:85 / 109
页数:25
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