Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Pegylated Interferon Alfa-2a Maintenance Therapy and Liver Disease Progression in People Infected With Both HIV and Hepatitis C Virus (HCV)

ClinicalTrials.gov ID: NCT00078403

Public ClinicalTrials.gov record NCT00078403. 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 27, 2026, 12:54 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Suppressive Long-Term Antiviral Management of Hepatitis C Virus (HCV) and HIV-1 Coinfected Subjects (SLAM-C)

Brief summary

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

Infection with both HIV and hepatitis C virus (HCV) may result in serious and sometimes fatal liver disease. The purpose of this study was to test the effectiveness of long-term pegylated interferon alfa-2a (PEG-IFN) and ribavirin treatment in slowing liver disease progression in people infected with both HIV and HCV.

Study identification

NCT ID
NCT00078403
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
333 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
Jul 2004 (Type not available)
Primary completion
May 2007 (Actual)
Completion
Feb 2009 (Actual)
Last update posted
Nov 8, 2021

2004 – 2009

United States locations

U.S. sites
36
U.S. states
18
U.S. cities
26
Facility City State ZIP Site status
Alabama Therapeutics CRS Birmingham Alabama 35924-2050 —
University of Southern California CRS Los Angeles California 90033-1079 —
UCLA CARE Center CRS Los Angeles California 90035 —
Stanford AIDS Clinical Trials Unit CRS Palo Alto California 94304-5350 —
UCSD Antiviral Research Center CRS San Diego California 92103 —
Ucsf Hiv/Aids Crs San Francisco California 94110 —
Santa Clara Valley Med. Ctr. San Jose California 95128 —
University of Colorado Hospital CRS Aurora Colorado 80045 —
Georgetown University CRS (GU CRS) Washington D.C. District of Columbia 20007 —
Univ. of Hawaii at Manoa, Leahi Hosp. Honolulu Hawaii 96816 —
Northwestern University CRS Chicago Illinois 60611 —
Indiana Univ. School of Medicine, Infectious Disease Research Clinic Indianapolis Indiana 46202-5250 —
Indiana Univ. School of Medicine, Wishard Memorial Indianapolis Indiana 46202-5250 —
Johns Hopkins University CRS Baltimore Maryland 21205 —
Massachusetts General Hospital CRS (MGH CRS) Boston Massachusetts 02114 —
Brigham and Women's Hosp. ACTG CRS Boston Massachusetts 02115 —
Beth Israel Deaconess Med. Ctr., ACTG CRS Boston Massachusetts 02215 —
Washington University Therapeutics (WT) CRS St Louis Missouri 63110-1010 —
Univ. of Nebraska Med. Ctr., Durham Outpatient Ctr. Omaha Nebraska 68198-9500 —
Beth Israel Med. Ctr., ACTU New York New York 10003 —
Weill Cornell Chelsea CRS New York New York 10011 —
NY Univ. HIV/AIDS CRS New York New York 10016 —
Weill Cornell Uptown CRS New York New York 10021 —
Columbia P&S CRS New York New York 10032-3732 —
Trillium Health ACTG CRS Rochester New York 14607 —
McCree McCuller Wellness Ctr. at the Connection, Infectious Disease Unit Rochester New York 14642 —
Univ. of Rochester ACTG CRS Rochester New York 14642 —
Chapel Hill CRS Chapel Hill North Carolina 27599 —
Cincinnati CRS Cincinnati Ohio 45267-0405 —
MetroHealth CRS Cleveland Ohio 44109 —
Univ. of Pennsylvania Health System, Presbyterian Med. Ctr. Philadelphia Pennsylvania 19104 —
University of Pittsburgh CRS Pittsburgh Pennsylvania 15213 —
The Miriam Hospital Clinical Research Site (TMH CRS) CRS Providence Rhode Island 02906 —
Vanderbilt Therapeutics (VT) CRS Nashville Tennessee 37204 —
Univ. of Texas Southwestern Med. Ctr., Amelia Court Continuity Clinic Dallas Texas 75235-9173 —
Univ. of Texas Medical Branch, ACTU Galveston Texas 77555-0435 —

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00078403, 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 Nov 8, 2021 · Synced Oct 27, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00078403 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →