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Completed Phase 3 Interventional Results available

Safety and Efficacy of SOF/VEL/VOX FDC for 8 Weeks and SOF/VEL for 12 Weeks in Adults Chronic Genotype 3 HCV Infection and Cirrhosis

ClinicalTrials.gov ID: NCT02639338

Public ClinicalTrials.gov record NCT02639338. 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 Jul 21, 2026, 6:43 PM 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 8 Weeks and Sofosbuvir/Velpatasvir for 12 Weeks in Subjects With Chronic Genotype 3 HCV Infection and Cirrhosis

Study identification

NCT ID
NCT02639338
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Gilead Sciences
Industry
Enrollment
220 participants

Conditions and interventions

Interventions

  • SOF/VEL/VOX Drug
  • SOF/VEL Drug

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 22, 2015
Primary completion
Oct 11, 2016
Completion
Jan 1, 2017
Last update posted
Mar 4, 2019

2015 – 2017

United States locations

U.S. sites
30
U.S. states
19
U.S. cities
30
Facility City State ZIP Site status
Not listed Long Beach California
Not listed Los Angeles California
Not listed Palo Alto California
Not listed Rialto California
Not listed San Diego California
Not listed San Francisco California
Not listed Aurora Colorado
Not listed Miami Florida
Not listed Wellington Florida
Not listed Atlanta Georgia
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 Hillsborough New Jersey
Not listed New York New York
Not listed The Bronx New York
Not listed Asheville North Carolina
Not listed Fayetteville North Carolina
Not listed Pittsburgh Pennsylvania
Not listed Providence Rhode Island
Not listed Nashville Tennessee
Not listed San Antonio Texas
Not listed Murray Utah
Not listed Norfolk Virginia
Not listed Richmond Virginia
Not listed Seattle Washington

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 40 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02639338, 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 4, 2019 · Synced Jul 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02639338 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →