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Completed Phase 3 Interventional Results available

Efficacy and Safety of Sofosbuvir Plus Ribavirin in Chronic Genotype 1, 2 and 3 Hepatitis C Virus (HCV) and Human Immunodeficiency Virus (HIV) Co-infected Adults

ClinicalTrials.gov ID: NCT01667731

Public ClinicalTrials.gov record NCT01667731. 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 22, 2026, 9:45 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, Open-label Study to Investigate the Efficacy and Safety of GS-7977 Plus Ribavirin in Chronic Genotype 1, 2 and 3 Hepatitis C Virus (HCV) and Human Immunodeficiency Virus (HIV) Co-infected Subjects

Study identification

NCT ID
NCT01667731
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Gilead Sciences
Industry
Enrollment
224 participants

Conditions and interventions

Interventions

  • SOF Drug
  • RBV 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, 2012
Primary completion
Oct 31, 2013
Completion
Jan 31, 2014
Last update posted
Nov 20, 2014

2012 – 2014

United States locations

U.S. sites
26
U.S. states
15
U.S. cities
26
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Coronado California
Not listed Los Angeles California
Not listed Lutherville California
Not listed Oakland California
Not listed Sacramento California
Not listed San Francisco California
Not listed Torrance California
Not listed Washington D.C. District of Columbia
Not listed Miami Florida
Not listed Orlando Florida
Not listed Tampa Florida
Not listed Chicago Illinois
Not listed Springfield Massachusetts
Not listed Kansas City Missouri
Not listed Hillsborough New Jersey
Not listed Santa Fe New Mexico
Not listed New York New York
Not listed Chapel Hill North Carolina
Not listed Durham North Carolina
Not listed Allentown Pennsylvania
Not listed Philadelphia Pennsylvania
Not listed Providence Rhode Island
Not listed Dallas Texas
Not listed Houston Texas
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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01667731, 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 20, 2014 · Synced Jul 22, 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 NCT01667731 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →