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Completed Phase 3 Interventional Results available

Comparison of Sofosbuvir/Velpatasvir Fixed Dose Combination for 12 Weeks With Sofosbuvir and Ribavirin for 24 Weeks in Adults With Chronic Genotype 3 HCV Infection

ClinicalTrials.gov ID: NCT02201953

Public ClinicalTrials.gov record NCT02201953. 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 Apr 29, 2026, 9:09 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, Multicenter, Randomized, Open-Label Study to Compare the Efficacy and Safety of Sofosbuvir/GS-5816 Fixed Dose Combination for 12 Weeks With Sofosbuvir and Ribavirin for 24 Weeks in Subjects With Chronic Genotype 3 HCV Infection

Study identification

NCT ID
NCT02201953
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Gilead Sciences
Industry
Enrollment
558 participants

Conditions and interventions

Interventions

  • RBV Drug
  • SOF 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
Jun 30, 2014
Primary completion
Aug 31, 2015
Completion
Nov 30, 2015
Last update posted
Nov 15, 2018

2014 – 2015

United States locations

U.S. sites
25
U.S. states
15
U.S. cities
24
Facility City State ZIP Site status
Not listed Los Angeles California 90027
Not listed Los Angeles California 90048
Not listed Sacramento California
Not listed San Diego California
Not listed Aurora Colorado
Not listed Gainesville Florida
Not listed Jacksonville Florida
Not listed Miami Florida
Not listed Orlando Florida
Not listed Wellington Florida
Not listed Marietta Georgia
Not listed Chicago Illinois
Not listed Indianapolis Indiana
Not listed Lutherville Maryland
Not listed Boston Massachusetts
Not listed Detroit Michigan
Not listed New York New York
Not listed The Bronx New York
Not listed Durham North Carolina
Not listed Philadelphia Pennsylvania
Not listed Pittsburgh Pennsylvania
Not listed Germantown Tennessee
Not listed San Antonio Texas
Not listed Norfolk Virginia
Not listed Richmond Virginia

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 51 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02201953, 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 Nov 15, 2018 · Synced Apr 29, 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 NCT02201953 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →