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Terminated Phase 4 Interventional Results available

Telaprevir, Peg-IFN-alfa-2a, and RBV in Treatment-Experienced Black/African American and Non-Black/African American Subjects With Genotype 1 Chronic Hepatitis C

ClinicalTrials.gov ID: NCT01467492

Public ClinicalTrials.gov record NCT01467492. 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 Sep 2, 2026, 1:40 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

An Open-Label, Phase 4 Study of Telaprevir, Peginterferon Alfa-2a (Pegasys®), and Ribavirin (Copegus®) in Treatment-Experienced Black/African American and Non-Black/African American Subjects With Genotype 1 Chronic Hepatitis C Who Have Not Achieved a Sustained Viral Response With a Prior Course of Interferon-Based Therapy

Brief summary

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

The purpose of this study is to evaluate the efficacy and safety of telaprevir in combination with pegylated interferon alfa 2a (Peg-IFN-alfa-2a) and ribavirin (RBV) in treatment-experienced Black/African American and non-Black/African American participants with Genotype 1 Chronic Hepatitis C (CHC), who have not achieved a sustained viral response with a prior course of interferon-based therapy.

Study identification

NCT ID
NCT01467492
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Enrollment
121 participants

Conditions and interventions

Conditions

Interventions

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
Dec 31, 2011
Primary completion
Apr 30, 2014
Completion
Apr 30, 2014
Last update posted
Aug 2, 2015

2012 – 2014

United States locations

U.S. sites
27
U.S. states
18
U.S. cities
27
Facility City State ZIP Site status
Alabama Birmingham Alabama
California San Francisco California
Connecticut New Haven Connecticut
Washington, DC Washington D.C. District of Columbia
Florida Miami Florida
Florida Orlando Florida
Florida Tampa Florida
Florida West Palm Beach Florida
Georgia Atlanta Georgia
Illinois Chicago Illinois
Louisiana Baton Rouge Louisiana
Louisiana New Orleans Louisiana
Louisiana Shreveport Louisiana
Maryland Baltimore Maryland
Massachusetts Boston Massachusetts
Michigan Detroit Michigan
New Jersey Vineland New Jersey
New York New York New York
New York The Bronx New York
North Carolina Charlotte North Carolina
North Carolina Durham North Carolina
Pennsylvania Philadelphia Pennsylvania
Texas Dallas Texas
Texas Houston Texas
Texas San Antoinio Texas
Virginia Norfolk Virginia
Washington 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01467492, 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 Aug 2, 2015 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01467492 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →