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Completed Phase 2 Interventional Results available

Safety and Efficacy of Voxilaprevir Plus Sofosbuvir/Velpatasvir Fixed Dose Combination in Adults With Chronic Genotype 1 HCV Infection

ClinicalTrials.gov ID: NCT02378935

Public ClinicalTrials.gov record NCT02378935. 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 17, 2026, 2:58 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 2, Global, Multicenter, Open-Label Study to Investigate the Safety and Efficacy of GS-9857 Plus Sofosbuvir/GS-5816 Fixed Dose Combination in Subjects With Chronic Genotype 1 HCV Infection

Brief summary

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

This primary objectives of the study are to evaluate the safety, tolerability, and efficacy of voxilaprevir (VOX) plus sofosbuvir/velpatasvir (SOF/VEL) fixed dose combination (FDC) ± ribavirin (RBV) in adults with chronic genotype 1 hepatitis C virus (HCV) infection.

Study identification

NCT ID
NCT02378935
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Gilead Sciences
Industry
Enrollment
205 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 17, 2015 (Actual)
Primary completion
Feb 1, 2016 (Actual)
Completion
Apr 12, 2016 (Actual)
Last update posted
Mar 6, 2020

2015 – 2016

United States locations

U.S. sites
31
U.S. states
18
U.S. cities
29
Facility City State ZIP Site status
Cedars Sinai Medical Center Los Angeles California — —
Stanford University Palo Alto California — —
Huntington Memorial Hospital Liver Center Pasadena California — —
Medical Associates Research Group, Inc. San Diego California — —
University of Colorado Denver Colorado — —
Borland-Groover Clinic Jacksonville Florida — —
University of Miami Miami Florida — —
Orlando Immunology center Orlando Florida — —
South Florida Center of Gastroenterology, P.A. Wellington Florida — —
Center for Hep C/Atlanta Medical Center Atlanta Georgia — —
Gastrointestinal Specialists of Georgia, PC Marietta Georgia — —
University of Chicago Chicago Illinois — —
Indiana University Indianapolis Indiana — —
Indianapolis Gastroenterology & Hepatology, Inc. Indianapolis Indiana — —
Beth Isreal Deconess Medical Center Boston Massachusetts — —
Massachusetts General Hospital Boston Massachusetts — —
Henry Ford Hospital and Health System Detroit Michigan — —
ID Care Hillsborough New Jersey — —
Southwest Care Center Santa Fe New Mexico — —
North Shore/Long Island Jewish PRIME Manhasset New York — —
Mount Sinai Beth Israel New York New York — —
Cumberland Research Associates, LLC Fayetteville North Carolina — —
Digestive Health Specialists, PA Winston-Salem North Carolina — —
University of Pennsylvania Health Systems Philadelphia Pennsylvania — —
UPMC Center for Liver Diseases Pittsburgh Pennsylvania — —
Medical University of South Carolina Charleston South Carolina — —
Gastro One Germantown Tennessee — —
Nashville Gastrointestinal Specialists, Inc. Nashville Tennessee — —
Texas Liver Institute San Antonio Texas — —
Liver Institute of Virginia Richmond Virginia — —
Swedish Medical Center 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 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02378935, 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 6, 2020 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02378935 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →