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Completed Phase 3 Interventional Results available

Sofosbuvir/Velpatasvir Fixed Dose Combination for 12 Weeks in Adults With Chronic HCV Infection

ClinicalTrials.gov ID: NCT02201940

Public ClinicalTrials.gov record NCT02201940. 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, 9:15 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, Double-Blind, Placebo-Controlled Study to Investigate the Efficacy and Safety of Sofosbuvir/GS-5816 Fixed Dose Combination for 12 Weeks in Subjects With Chronic HCV

Study identification

NCT ID
NCT02201940
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Gilead Sciences
Industry
Enrollment
741 participants

Conditions and interventions

Interventions

  • Placebo 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
May 31, 2015
Completion
Aug 31, 2015
Last update posted
Nov 14, 2018

2014 – 2015

United States locations

U.S. sites
34
U.S. states
16
U.S. cities
30
Facility City State ZIP Site status
Not listed Little Rock Arkansas
Not listed Long Beach California
Not listed Los Angeles California 90027
Not listed Los Angeles California 90036
Not listed Los Angeles California 90048
Not listed Palo Alto California
Not listed Sacramento California
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
Not listed Miami Florida
Not listed Orlando Florida
Not listed Wellington Florida
Not listed Atlanta Georgia 30308
Not listed Marietta Georgia
Not listed Chicago Illinois 60611
Not listed Indianapolis Indiana 46237
Not listed Baltimore Maryland
Not listed Lutherville Maryland 21093
Not listed Boston Massachusetts 02215
Not listed Detroit Michigan 48188
Not listed New York New York 10021
Not listed The Bronx New York 10468
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
Not listed Nashville Tennessee
Not listed San Antonio Texas 78215
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 46 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02201940, 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 14, 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 NCT02201940 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →