Sofosbuvir-velpatasvir successful in hep C regardless of genotype
Jordan J. Feld, M.D., M.P.H., from the Toronto Western Hospital Liver Centre, and colleagues conducted a phase 3 study involving patients with HCV genotypes 1, 2, 4, 5, or 6, who were randomized to receive sofosbuvir and velpatasvir or matching placebo. The researchers found that among the 624 patients receiving sofosbuvir-velpatasvir, the rate of sustained virologic response was 99 percent at 12 weeks after the end of therapy; two patients had a virologic relapse.
Michael P. Curry, M.D., from the Beth Israel Deaconess Medical Center in Boston, and colleagues conducted a phase 3 study involving 267 patients with HCV genotypes 1 through 6 who had decompensated cirrhosis. Participants were randomized to 12 weeks of sofosbuvir-velpatasvir or sofosbuvir-velpatasvir plus ribavirin, or to 24 weeks of sofosbuvir-velpatasvir. The researchers found that the overall sustained virologic response was 83, 94, and 86 percent, respectively, with no significant between-group differences. In a third study, Graham R. Foster, Ph.D., from the Queen Mary University of London, and colleagues found that 12 weeks of sofosbuvir-velpatasvir treatment resulted in superior rates of sustained virologic response versus sofosbuvir-ribavirin among patients with HCV genotype 2 or 3.
"These studies indicate that this drug regimen can achieve high rates of HCV cure regardless of genotype," write the authors of an accompanying editorial.
All three studies were funded by Gilead Sciences, the manufacturer of sofosbuvir-velpatasvir.
Abstract - Curry
Abstract - Foster
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