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Completed Phase 4 Interventional Results available

REPEAT Study - A Study of PEGASYS (Peginterferon Alfa-2a (40KD)) Therapy in Combination With COPEGUS (Ribavirin) in Patients With Chronic Hepatitis C (CHC) Who Did Not Respond to Previous PegIntron (Peginterferon Alfa-2b (12KD))/Ribavirin Combination Therapy

ClinicalTrials.gov ID: NCT00087646

Public ClinicalTrials.gov record NCT00087646. 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 3, 2026, 1:47 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 Randomized, Open-label Study of the Effect of PEGASYS Combined With Ribavirin on Sustained Virologic Response in Patients With Chronic Hepatitis C Who Did Not Respond to Previous Pegintron/Ribavirin Combination Therapy

Brief summary

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

This 4 arm study is designed for patients with CHC who have not responded to peginterferon alfa-2b (12KD)/ribavirin combination therapy. In these patients, the effects of lengthening the duration of treatment, as well as including an initial 12-week period of high-dose PEGASYS (360 micrograms sc), are compared with the standard combination therapy of PEGASYS (180 micrograms sc) and ribavirin (1000-1200mg po). The anticipated time on study treatment is 1-2 years and the target sample size is 500+ individuals.

Study identification

NCT ID
NCT00087646
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
948 participants

Conditions and interventions

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
Aug 31, 2003
Primary completion
Apr 30, 2008
Completion
Apr 30, 2008
Last update posted
Jan 13, 2016

2003 – 2008

United States locations

U.S. sites
36
U.S. states
22
U.S. cities
33
Facility City State ZIP Site status
Not listed Mobile Alabama 36693
Not listed Scottsdale Arizona 85259
Not listed Los Angeles California 90033
Not listed Pasadena California 91105
Not listed San Diego California 92123
Not listed Ukiah California 95482
Not listed Farmington Connecticut 06030
Not listed Bradenton Florida 34243
Not listed Hollywood Florida 33021
Not listed Jacksonville Florida 32256
Not listed Atlanta Georgia 30308
Not listed Atlanta Georgia 30309
Not listed Savannah Georgia 31404
Not listed Chicago Illinois 60611
Not listed Chicago Illinois 60612
Not listed Des Moines Iowa 50312
Not listed Baltimore Maryland 21224
Not listed Boston Massachusetts 02114
Not listed Boston Massachusetts 02215
Not listed Minneapolis Minnesota 55404-4565
Not listed Rochester Minnesota 55905
Not listed Kansas City Missouri 64131
Not listed St Louis Missouri 63110
Not listed Florham Park New Jersey
Not listed Albuquerque New Mexico 87131
Not listed Williamsville New York 14221
Not listed Lancaster Pennsylvania 17604-3200
Not listed Philadelphia Pennsylvania 19104
Not listed Cranston Rhode Island 02920
Not listed Memphis Tennessee 38120
Not listed Nashville Tennessee 37211
Not listed Austin Texas 78758
Not listed Houston Texas 77054
Not listed Salt Lake City Utah 84121
Not listed Burlington Vermont 05401
Not listed Richmond Virginia 23249

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 68 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00087646, 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 Jan 13, 2016 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00087646 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →