| Literature DB >> 31230974 |
John O Link1, James G Taylor2, Alejandra Trejo-Martin2, Darryl Kato2, Ashley A Katana2, Evan S Krygowski2, Zheng-Yu Yang2, Sheila Zipfel2, Jeromy J Cottell2, Elizabeth M Bacon2, Chinh V Tran2, Cheng Y Yang3, Yujin Wang3, Kelly W Wang3, Guangyu Zhao3, Guofeng Cheng4, Yang Tian4, Ruoyu Gong4, Yu-Jen Lee4, Mei Yu4, Eric Gorman5, Erik Mogalian5, Jason K Perry6.
Abstract
Direct-acting antiviral inhibitors have revolutionized the treatment of hepatitis C virus (HCV) infected patients. Herein is described the discovery of velpatasvir (VEL, GS-5816), a potent pan-genotypic HCV NS5A inhibitor that is a component of the only approved pan-genotypic single-tablet regimens (STRs) for the cure of HCV infection. VEL combined with sofosbuvir (SOF) is Epclusa®, an STR with 98% cure-rates for genotype 1-6 HCV infected patients. Addition of the pan-genotypic HCV NS3/4A protease inhibitor voxilaprevir to SOF/VEL is the STR Vosevi®, which affords 97% cure-rates for genotype 1-6 HCV patients who have previously failed another treatment regimen.Entities:
Keywords: DAA; Direct-acting-antiviral; Epclusa(®); GS-5816; HCV; Hepatitis C Virus; NS5A; Non-structural protein 5A; Rule-of-five; SVR; Single-tablet regimen; Sofosbuvir; Sustained viral response; Velpatasvir
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Year: 2019 PMID: 31230974 DOI: 10.1016/j.bmcl.2019.04.027
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823