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Completed Phase 3 Interventional Results available

Phase 3 Efficacy and Safety Study of Peginterferon Lambda-1a and Ribavirin With Telaprevir

ClinicalTrials.gov ID: NCT01598090

Public ClinicalTrials.gov record NCT01598090. 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 11, 2026, 12:09 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 Blinded Randomized Study of Peginterferon Lambda-1a and Ribavirin Compared to Peginterferon Alfa-2a and Ribavirin, Each Administered With Telaprevir in Subjects With Genotype-1 Chronic Hepatitis C Who Are Treatment-naive or Relapsed on Prior Treatment With Peginterferon Alfa-2a and Ribavirin

Brief summary

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

The purpose of this study is to determine whether Peginterferon Lambda-1a (Lambda) combined with Ribavirin (RBV) and Telaprevir (TVR) is effective in the treatment of chronic Hepatitis C (CHC) compared to Peginterferon Alfa-2a (alfa-2a) combined with RBV and Telaprevir.

Study identification

NCT ID
NCT01598090
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
881 participants

Conditions and interventions

Interventions

Biological · Drug

Eligibility (public fields only)

Age range
Not listed
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 13, 2012
Primary completion
Feb 3, 2015
Completion
May 14, 2015
Last update posted
Jul 30, 2019

2012 – 2015

United States locations

U.S. sites
28
U.S. states
12
U.S. cities
23
Facility City State ZIP Site status
Birmingham Gastroenterology Associates, P.C. Birmingham Alabama 35209
The Kirklin Clinic Birmingham Alabama 35294
The University Of Alabama Of Birmingham Birmingham Alabama 35294
Anaheim Clinical Trials Llc Anaheim California 92801
Sc Clinical Research, Inc. Garden Grove California 92844
Va Long Beach Healthcare System Long Beach California 90822
Cedars Sinai Medical Center Los Angeles California 90048
Va Greater Los Angeles Healthcare System Los Angeles California 90073
University Of California, San Francisco/Sf General Hospital San Francisco California 94110
South Bay Ge Medical Group Torrance California 90505
Orlando Va Medical Center Orlando Florida 32803
Orlando Clinical Research Center Orlando Florida 32809
Infectious Disease Research Institute, Inc. Tampa Florida 33614
Gastrointestinal Specialists Of Georgia Pc Marietta Georgia 30060
Mercy Medical Center Baltimore Maryland 21202
Saint Luke'S Transplant Specialists Kansas City Missouri 64111
Saint Louis University St Louis Missouri 63104
Carolinas Medical Center Charlotte North Carolina 28204
Options Health Research, Llc Tulsa Oklahoma 74104
Healthcare Research Consultants Tulsa Oklahoma 74135
Gastro One Germantown Tennessee 38138
Texas Clinical Research Institute Arlington Texas 76012
Brooke Army Medical Center Fort Sam Houston Texas 78234
Alamo Medical Research San Antonio Texas 78215
Clinical Research Centers Of America Murray Utah 84123
Metropolitan Research Annandale Virginia 22003
Bon Secours St. Mary'S Hospital Of Richmond, Inc. Newport News Virginia 23602
Digestive And Liver Disease Specialists Norfolk Virginia 23502

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 76 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01598090, 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 Jul 30, 2019 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01598090 live on ClinicalTrials.gov.

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