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Completed Phase 3 Interventional Results available

Safety and Efficacy of SOF/VEL/VOX FDC for 12 Weeks and SOF/VEL for 12 Weeks in DAA-Experienced Adults With Chronic HCV Infection Who Have Not Received an NS5A Inhibitor

ClinicalTrials.gov ID: NCT02639247

Public ClinicalTrials.gov record NCT02639247. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 11:04 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Global, Multicenter, Randomized, Open-Label Study to Investigate the Safety and Efficacy of Sofosbuvir/Velpatasvir/GS-9857 Fixed-Dose Combination for 12 Weeks and Sofosbuvir/Velpatasvir for 12 Weeks in Direct-Acting Antiviral-Experienced Subjects With Chronic HCV Infection Who Have Not Received an NS5A Inhibitor

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objectives of the study are to evaluate the efficacy, safety, and tolerability of treatment with sofosbuvir/velpatasvir/voxilaprevir (Vosevi®; SOF/VEL/VOX) fixed-dose combination (FDC) for 12 weeks and of sofosbuvir/velpatasvir (Epclusa®; SOF/VEL) FDC for 12 weeks in direct-acting antiviral (DAA)-experienced adults with chronic hepatitis C virus (HCV) infection with or without cirrhosis who have not received prior treatment with a regimen containing an inhibitor of the HCV NS5A protein.

Study identification

NCT ID
NCT02639247
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Gilead Sciences
Industry
Enrollment
333 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 23, 2015 (Actual)
Primary completion
Oct 5, 2016 (Actual)
Completion
Jan 18, 2017 (Actual)
Last update posted
Mar 5, 2019

2015 – 2017

United States locations

U.S. sites
43
U.S. states
23
U.S. cities
43
Facility City State ZIP Site status
Not listed Long Beach California — —
Not listed Los Angeles California — —
Not listed Palo Alto California — —
Not listed Pasadena California — —
Not listed Rialto California — —
Not listed San Diego California — —
Not listed San Francisco California — —
Not listed Aurora Colorado — —
Not listed Englewood Colorado — —
Not listed Washington D.C. District of Columbia — —
Not listed Gainesville Florida — —
Not listed Miami Florida — —
Not listed Orlando Florida — —
Not listed Wellington Florida — —
Not listed Atlanta Georgia — —
Not listed Marietta Georgia — —
Not listed Chicago Illinois — —
Not listed Indianapolis Indiana — —
Not listed Bastrop Louisiana — —
Not listed Baltimore Maryland — —
Not listed Catonsville Maryland — —
Not listed Boston Massachusetts — —
Not listed Ann Arbor Michigan — —
Not listed Detroit Michigan — —
Not listed Kansas City Missouri — —
Not listed St Louis Missouri — —
Not listed Hillsborough New Jersey — —
Not listed New York New York — —
Not listed Asheville North Carolina — —
Not listed Fayetteville North Carolina — —
Not listed Philadelphia Pennsylvania — —
Not listed Pittsburgh Pennsylvania — —
Not listed Providence Rhode Island — —
Not listed Germantown Tennessee — —
Not listed Nashville Tennessee — —
Not listed Houston Texas — —
Not listed San Antonio Texas — —
Not listed Murray Utah — —
Not listed Falls Church Virginia — —
Not listed Norfolk Virginia — —
Not listed Richmond Virginia — —
Not listed Seattle Washington — —
Not listed Madison Wisconsin — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 35 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02639247, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 5, 2019 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02639247 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →