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Characterization of HCV resistance from a 3-day monotherapy study of voxilaprevir, a novel pangenotypic NS3/4A protease inhibitor.
Antiviral Therapy ( IF 1.2 ) Pub Date : 2017-10-25 , DOI: 10.3851/imp3202
Eric Lawitz 1 , Jenny C Yang 2 , Luisa M Stamm 2 , James G Taylor 2 , Guofeng Cheng 2 , Diana M Brainard 2 , Michael D Miller 2 , Hongmei Mo 2 , Hadas Dvory-Sobol 2
Affiliation  

Voxilaprevir (VOX; GS-9857) is a pangenotypic HCV NS3/4A protease inhibitor (PI) with potent antiviral activity against HCV genotypes (GTs) 1-6 and improved coverage of GT1 NS3 resistance-associated substitutions (RAS) associated with other HCV PIs. In a 3-day Phase Ib monotherapy study in patients infected with HCV GT1a, 1b, 2, 3 and 4, VOX was well-tolerated and resulted in maximal mean viral load reduction >3 log10 IU/ml at the 100 mg dose across all genotypes evaluated. This report characterizes the HCV NS3 RAS in the study.

中文翻译:

新型泛基因型NS3 / 4A蛋白酶抑制剂voxilaprevir为期3天的单药治疗研究表明,HCV耐药。

Voxilaprevir(VOX; GS-9857)是一种全基因型HCV NS3 / 4A蛋白酶抑制剂(PI),具有针对HCV基因型(GTs)1-6的有效抗病毒活性,并改善了与其他HCV相关的GT1 NS3耐药相关取代(RAS)的覆盖范围效绩指标。在一项为期3天的Ib期单药治疗研究中,HCV GT1a,1b,2、3和4感染的患者对VOX的耐受性良好,在100 mg剂量范围内,最大平均病毒载量降低> 3 log 10 IU / ml评估所有基因型。该报告表征了研究中的HCV NS3 RAS。
更新日期:2020-08-21
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