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Completed Phase 4 Interventional

Study Of Investigational Regimen Combining FDA Approved HIV Drugs In HIV Subjects Experiencing Early Virologic Failure

ClinicalTrials.gov ID: NCT00038506

Public ClinicalTrials.gov record NCT00038506. 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 22, 2026, 4:37 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 IV, Open-label, Multicenter Study of Treatment With TRIZIVIR (Abacavir 300mg/Lamivudine 150mg/Zidovudine 300mg) Twice Daily and Tenofovir 300mg Once-daily for 48 Weeks in HIV-infected Subjects Experiencing Early Virologic Failure (ZIAGEN Intensification Protocol)

Brief summary

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

This study is a 48-week study to evaluate the efficacy and safety of an investigational regimen combining FDA approved HIV drugs in antiretroviral-experienced subjects failing on their first highly active antiretroviral therapy regimen.

Study identification

NCT ID
NCT00038506
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
ViiV Healthcare
Industry
Enrollment
100 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
Mar 2002 (Type not available)
Primary completion
Aug 2004 (Actual)
Completion
Aug 2004 (Actual)
Last update posted
Apr 8, 2015

2002 – 2004

United States locations

U.S. sites
27
U.S. states
11
U.S. cities
25
Facility City State ZIP Site status
GSK Investigational Site Los Angeles California 90027 —
GSK Investigational Site San Rafael California 94903 —
GSK Investigational Site Fort Lauderdale Florida 33145 —
GSK Investigational Site Jacksonville Florida 32206 —
GSK Investigational Site Lake Worth Florida 33463 —
GSK Investigational Site Miami Florida 33136 —
GSK Investigational Site Miami Beach Florida 33139 —
GSK Investigational Site North Miami Florida 33161 —
GSK Investigational Site Orlando Florida 32804 —
GSK Investigational Site Tallahassee Florida 32303 —
GSK Investigational Site Atlanta Georgia 30309 —
GSK Investigational Site Decatur Georgia 30033 —
GSK Investigational Site Chicago Illinois 60657 —
GSK Investigational Site Maywood Illinois 60153 —
GSK Investigational Site Lafayette Indiana 47904 —
GSK Investigational Site Berkeley Michigan 48072 —
GSK Investigational Site New York New York 10014 —
GSK Investigational Site The Bronx New York 10461 —
GSK Investigational Site Valhalla New York 10595 —
GSK Investigational Site Tulsa Oklahoma 74114 —
GSK Investigational Site Arlington Texas 76015 —
GSK Investigational Site Dallas Texas 75208 —
GSK Investigational Site Dallas Texas 75216 —
GSK Investigational Site Dallas Texas 75246 —
GSK Investigational Site Houston Texas 77004 —
GSK Investigational Site Seattle Washington 98104 —
GSK Investigational Site Green Bay Wisconsin 54301 —

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 NCT00038506, 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 Apr 8, 2015 · Synced Oct 22, 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 NCT00038506 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →