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Completed Phase 2 Interventional

GS-5885 Alone or in Combination With GS-9451 With Peginterferon Alfa 2a and Ribavirin in Treatment Chronic Genotype 1 Hepatitis C Virus

ClinicalTrials.gov ID: NCT01356160

Public ClinicalTrials.gov record NCT01356160. 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 Jun 26, 2026, 12:01 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 2b, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating Response Guided Therapy With GS-5885 Alone or in Combination With GS-9451 With Peginterferon Alfa 2a and Ribavirin in Treatment Naïve Subjects With Chronic Genotype 1 Hepatitis C Virus Infection

Study identification

NCT ID
NCT01356160
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Gilead Sciences
Industry
Enrollment
351 participants

Conditions and interventions

Interventions

  • GS-5885 Drug
  • GS-9451 Drug
  • peginterferon alfa-2a Biological
  • ribavirin tablet Drug
  • GS-9451 Placebo Drug

Drug · Biological

Eligibility (public fields only)

Age range
18 Years to 70 Years
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, 2011
Primary completion
May 31, 2013
Completion
May 31, 2013
Last update posted
Feb 2, 2014

2011 – 2013

United States locations

U.S. sites
21
U.S. states
13
U.S. cities
20
Facility City State ZIP Site status
Not listed Tucson Arizona 85724
Not listed Beverly Hills California 90211
Not listed Coronado California 92118
Not listed Costa Mesa California 92626
Not listed San Diego California 92123
Not listed Aurora Colorado 80045
Not listed Englewood Colorado 80110
Not listed Bradenton Florida 34209
Not listed Baltimore Maryland 21202
Not listed Baltimore Maryland 21229
Not listed Burlington Massachusetts 01805
Not listed Kansas City Missouri 64131
Not listed Forest Hills New York 11375
Not listed Manhasset New York 11030
Not listed Durham North Carolina 27710
Not listed Cincinnati Ohio 45267
Not listed Nashville Tennessee 37211
Not listed Arlington Texas 76012
Not listed Houston Texas 77030
Not listed San Antonio Texas 78215
Not listed Fairfax Virginia 22031

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01356160, 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 Feb 2, 2014 · Synced Jun 26, 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 NCT01356160 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →