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Completed Phase 3 Interventional Results available

Sofosbuvir/Velpatasvir Fixed-Dose Combination in Adults With Chronic HCV Infection

ClinicalTrials.gov ID: NCT02346721

Public ClinicalTrials.gov record NCT02346721. 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 Sep 2, 2026, 3:50 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

An Open Label Study of Sofosbuvir/GS-5816 Fixed-Dose Combination in Subjects With Chronic HCV Infection

Brief summary

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

The primary objectives of this study are to evaluate the efficacy, safety, and tolerability of treatment with sofosbuvir/velpatasvir (SOF/VEL) in participants with chronic genotype 1, 2, 4, 6 or indeterminate HCV infection who received placebo in the Gilead-sponsored study GS-US-342-1138.

Study identification

NCT ID
NCT02346721
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Gilead Sciences
Industry
Enrollment
111 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
Feb 22, 2015
Primary completion
Mar 22, 2016
Completion
Jun 14, 2016
Last update posted
Nov 15, 2018

2015 – 2016

United States locations

U.S. sites
25
U.S. states
11
U.S. cities
21
Facility City State ZIP Site status
Not listed Long Beach California 90822
Not listed Los Angeles California 90027
Not listed Los Angeles California 90036
Not listed Los Angeles California 90048
Not listed Palo Alto California 94304
Not listed Sacramento California 95817
Not listed San Diego California 92123
Not listed San Diego California 92154
Not listed Aurora Colorado 80045
Not listed Gainesville Florida 32610-0272
Not listed Jacksonville Florida 32256
Not listed Miami Florida 33136
Not listed Wellington Florida 33414
Not listed Atlanta Georgia 30308
Not listed Marietta Georgia 30066
Not listed Indianapolis Indiana 46237
Not listed Baltimore Maryland 21202
Not listed Boston Massachusetts 02129
Not listed Philadelphia Pennsylvania 19104
Not listed Pittsburgh Pennsylvania 15213
Not listed Pittsburgh Pennsylvania 15240
Not listed Providence Rhode Island 02905
Not listed Germantown Tennessee 38138
Not listed Nashville Tennessee 37211
Not listed Richmond Virginia 23226

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 36 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02346721, 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 Sep 2, 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 NCT02346721 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →