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Completed Phase 3 Interventional Results available

A Study of Pegasys (Peginterferon Alfa-2a) Administered Alone or in Combination With Copegus (Ribavirin) in Patients With Chronic Hepatitis C Who Have Participated in Previous Pegasys Trials

ClinicalTrials.gov ID: NCT01853254

Public ClinicalTrials.gov record NCT01853254. 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 Oct 20, 2026, 4:51 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 Protocol Providing Pegylated Interferon Alfa-2a (Pegasys®) as Monotherapy or in Combination With Ribavirin (Copegus®) for Patients With Chronic Hepatitis C Who Have Participated in Previous Roche or Roche Partner Protocols

Brief summary

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

This open-label, non-randomized, single arm study will provide treatment or re-treatment with Pegasys (peginterferon alfa-2a) as monotherapy or in combination with Copegus (ribavirin) to patients with chronic hepatitis C infection. Patients who have received prior Pegasys monotherapy or combination therapy or who were considered eligible for treatment with Pegasys in previous donor protocols will be eligible to participate in this study. Treatment will be on investigator's decision according to the approved label for up to 48 weeks, with a 24-week safety follow-up.

Study identification

NCT ID
NCT01853254
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
272 participants

Conditions and interventions

Interventions

Drug

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
Sep 2003 (Type not available)
Primary completion
Sep 2011 (Actual)
Completion
Sep 2011 (Actual)
Last update posted
Sep 4, 2013

2003 – 2011

United States locations

U.S. sites
49
U.S. states
24
U.S. cities
44
Facility City State ZIP Site status
Not listed Birmingham Alabama 35295-0005 —
Not listed La Jolla California 92037-1030 —
Not listed Long Beach California 90822 —
Not listed San Diego California 92123 —
Not listed San Diego California 92154 —
Not listed San Francisco California 94115 —
Not listed Aurora Colorado 80045 —
Not listed Gainesville Florida 32610-0214 —
Not listed Gainesville Florida 32610 —
Not listed Jacksonville Florida 32209 —
Not listed Miami Florida 33136-1051 —
Not listed Orlando Florida 32803 —
Not listed Orlando Florida 32809 —
Not listed Sarasota Florida 34243 —
Not listed Wellington Florida 33414 —
Not listed Atlanta Georgia 30308 —
Not listed Atlanta Georgia 30309 —
Not listed Marietta Georgia 30060 —
Not listed Honolulu Hawaii 96817 —
Not listed Boise Idaho 83702 —
Not listed Indianapolis Indiana 46202 —
Not listed Iowa City Iowa 52242 —
Not listed Kansas City Kansas 66160 —
Not listed Baltimore Maryland 21205 —
Not listed Framingham Massachusetts 01702 —
Not listed Worcester Massachusetts 01655 —
Not listed Plymouth Minnesota 55446 —
Not listed Newark New Jersey 07102 —
Not listed Vineland New Jersey 08360 —
Not listed Binghamton New York 13903 —
Not listed Manhasset New York 11030 —
Not listed New York New York 10016 —
Not listed New York New York 10021 —
Not listed Poughkeepsie New York 12601 —
Not listed Durham North Carolina 27710 —
Not listed Statesville North Carolina 28677 —
Not listed Cleveland Ohio 44106 —
Not listed Portland Oregon 97201 —
Not listed Lancaster Pennsylvania 17604-3200 —
Not listed Philadelphia Pennsylvania 19104 —
Not listed Providence Rhode Island 02905 —
Not listed Germantown Tennessee 38138 —
Not listed Dallas Texas 75203 —
Not listed Houston Texas 77030 —
Not listed San Antonio Texas 78215 —
Not listed Charlottesville Virginia 22906-0013 —
Not listed Bellevue Washington 98004 —
Not listed Seattle Washington 98133 —
Not listed Tacoma Washington 98403 —

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 18 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01853254, 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 Sep 4, 2013 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01853254 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →