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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 Oct 25, 2026, 6:06 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, 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

Brief summary

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

This study will evaluate the efficacy, safety, and tolerability of sofosbuvir (SOF; GS-7977) plus ribavirin (RBV) in adults with chronic genotypes 1, 2, and 3 HCV infection who are coinfected with HIV-1.

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

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
Jul 2012 (Type not available)
Primary completion
Nov 2013 (Actual)
Completion
Feb 2014 (Actual)
Last update posted
Nov 21, 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 21, 2014 · Synced Oct 25, 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 public registry record, listed eligibility criteria, and available contact information for NCT01667731 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →