Sofosbuvir/Velpatasvir: A Review in Chronic Hepatitis C

被引:53
作者
Greig, Sarah L. [1 ]
机构
[1] Springer, Private Bag 65901, Auckland 0754, New Zealand
关键词
DRUG-DRUG INTERACTION; PATIENT-REPORTED OUTCOMES; FIXED-DOSE COMBINATION; GENOTYPE; VIRUS-INFECTION; INTERACTION PROFILE; NS5A INHIBITOR; HCV; VELPATASVIR; SOFOSBUVIR;
D O I
10.1007/s40265-016-0648-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A once-daily, single-tablet, pangenotypic regimen comprising the hepatitis C virus (HCV) NS5B polymerase inhibitor sofosbuvir and the HCV NS5A inhibitor velpatasvir (sofosbuvir/velpatasvir; Epclusa(A (R))) was recently approved for the treatment of adults with chronic HCV genotype 1, 2, 3, 4, 5 or 6 infection in the USA, EU and Canada. In the phase III ASTRAL trials, once-daily oral sofosbuvir/velpatasvir for 12 weeks provided very high rates of sustained virological response at 12 weeks post treatment (SVR12) in treatment-naive and -experienced patients with chronic HCV genotype 1-6 infection, including those with compensated cirrhosis or HIV-1 co-infection. High SVR12 rates were also observed with sofosbuvir/velpatasvir plus ribavirin for 12 weeks in patients with chronic HCV genotype 1-6 infection and decompensated cirrhosis. Sofosbuvir/velpatasvir was generally well tolerated, with low rates of adverse events. Thus, sofosbuvir/velpatasvir represents a valuable treatment option in adults with chronic HCV genotype 1-6 infection, including those with compensated or decompensated cirrhosis, previous treatment experience or HIV-1 co-infection.
引用
收藏
页码:1567 / 1578
页数:12
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