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Completed Phase 4 Interventional Results available

A Study of PEGASYS (Peginterferon Alfa-2a (40KD)) in Combination With Ribavirin in Patients With Chronic Hepatitis C (CHC) Previously Treated With PEG-Intron + Ribavirin

ClinicalTrials.gov ID: NCT00087568

Public ClinicalTrials.gov record NCT00087568. 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, 4:08 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, Multicenter, Efficacy and Safety Study of Pegasys® Plus Ribavirin in Patients With Chronic HCV Infection Who Are Unable to Tolerate or Who Do Not Respond to 12 Weeks of Therapy With PEGIntron ® Plus Ribavirin

Brief summary

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

This study will evaluate the efficacy, safety and tolerability of PEGASYS plus ribavirin in patients with CHC who could not tolerate or were not responsive to 12 weeks of therapy with PEG-Intron plus ribavirin. The anticipated time on study treatment is 1-2 years, and the target sample size is \>100 individuals.

Study identification

NCT ID
NCT00087568
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
57 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
Dec 31, 2002
Primary completion
Feb 28, 2006
Completion
Feb 28, 2006
Last update posted
Jun 7, 2016

2003 – 2006

United States locations

U.S. sites
25
U.S. states
13
U.S. cities
25
Facility City State ZIP Site status
Not listed Bakersfield California 93301
Not listed Pasadena California 91105
Not listed San Diego California 92123
Not listed San Mateo California 94403
Not listed Bradenton Florida 34209
Not listed Miami Florida 33136-1051
Not listed Orlando Florida 32806
Not listed Austell Georgia 30106
Not listed Annapolis Maryland 21401
Not listed Baltimore Maryland 21229
Not listed Boston Massachusetts 02114
Not listed Kansas City Missouri 64131
Not listed Bayside New York 11358
Not listed Brooklyn New York 11219
Not listed Manhasset New York 11030
Not listed New York New York 10032
Not listed Valhalla New York 10595
Not listed Statesville North Carolina 28677
Not listed Cincinnati Ohio 45219
Not listed Knoxville Tennessee 37920
Not listed Memphis Tennessee 38120
Not listed Houston Texas 77054
Not listed Fairfax Virginia 22031
Not listed Richmond Virginia 23298
Not listed Tacoma Washington 98405

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 NCT00087568, 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 Jun 7, 2016 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00087568 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →