Sofosbuvir/Velpatasvir Fixed-Dose Combination and Ribavirin for 12 or 24 Weeks in Participants With Chronic Genotype 1 or 2 Hepatitis C Virus Infection Who Have Previously Failed a Direct-Acting Antiviral-Containing Regimen

PHASE3CompletedINTERVENTIONAL
Enrollment

117

Participants

Timeline

Start Date

July 25, 2016

Primary Completion Date

June 2, 2017

Study Completion Date

August 25, 2017

Conditions
Hepatitis C Virus Infection
Interventions
DRUG

SOF/VEL

400/100 mg tablet administered orally once daily

DRUG

RBV

Capsules administered orally in a divided daily dose according to package insert weight-based dosing recommendations (≤ 60 kg = 600 mg, \> 60 kg to ≤ 80 kg = 800 mg, and ≥ 80 kg = 1000 mg)

Trial Locations (18)

Unknown

Ehime

Hiroshima

Ichikawa-shi

Iruma-gun

Kashihara

Kurume-shi

Kyoto

Maebashi

Musashino-shi

Nagoya

Nishinomiya

Okayama

Ōgaki

Ōmura

Sapporo

Suita

Takamatsu

Yamagata

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Gilead Sciences

INDUSTRY