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Completed Phase 2 Interventional

Effectiveness of the Early Addition of Abacavir to an Anti-HIV Drug Combination

ClinicalTrials.gov ID: NCT00001132

Public ClinicalTrials.gov record NCT00001132. 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 9, 2026, 1:46 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 Pilot Study of Early Treatment Intensification of Antiretroviral Therapy

Brief summary

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

The purpose of this study is to see if adding 1 drug to an anti-HIV drug combination early in treatment against HIV can lower the viral load (amount of HIV in the blood) to a level so low that it cannot be measured (undetectable). The drug that will be added to a treatment is abacavir (ABC). Many patients who take 3 anti-HIV drugs together are able to achieve very low viral loads, for example, viral loads below 50 copies/ml. However, some patients taking only 3 drugs are not able to achieve a viral load this low. Doctors hope that, by adding the drug ABC to a current treatment, a viral load below 50 copies/ml can be achieved. Doctors would like to find out if it is effective to start patients on 3 drugs and then add another drug (treatment intensification) if the treatment is not working as well as hoped.

Study identification

NCT ID
NCT00001132
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
80 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
13 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
Oct 31, 1999
Primary completion
Not listed
Completion
Mar 31, 2001
Last update posted
Sep 8, 2008

1999 – 2001

United States locations

U.S. sites
29
U.S. states
15
U.S. cities
22
Facility City State ZIP Site status
UCLA CARE Ctr Los Angeles California 90095
Willow Clinic Menlo Park California 94025
Santa Clara Valley Med Ctr / AIDS Community Rsch Consortium San Jose California 951282699
San Mateo AIDS Program / Stanford Univ Stanford California 943055107
Stanford Univ Med Ctr Stanford California 943055107
Harbor UCLA Med Ctr Torrance California 90502
Univ of Colorado Health Sciences Ctr Denver Colorado 80262
Univ of Miami School of Medicine Miami Florida 331361013
Emory Univ Atlanta Georgia 30308
Northwestern Univ Med School Chicago Illinois 60611
Cook County Hosp Chicago Illinois 60612
State of MD Div of Corrections / Johns Hopkins Univ Hosp Baltimore Maryland 212052196
Johns Hopkins Hosp Baltimore Maryland 21287
St Louis Regional Hosp / St Louis Regional Med Ctr St Louis Missouri 63112
SUNY / Erie County Med Ctr at Buffalo Buffalo New York 14215
Beth Israel Med Ctr New York New York 10003
Bellevue Hosp / New York Univ Med Ctr New York New York 10016
Aaron Diamond AIDS Rsch Ctr / Rockefeller Univ New York New York 10021
Columbia Presbyterian Med Ctr New York New York 10032
Univ of Rochester Medical Center Rochester New York 14642
Univ of North Carolina Chapel Hill North Carolina 275997215
Duke Univ Med Ctr Durham North Carolina 27710
Univ of Cincinnati Cincinnati Ohio 452670405
Philadelphia Veterans Administration Med Ctr Philadelphia Pennsylvania 19104
Univ of Pennsylvania at Philadelphia Philadelphia Pennsylvania 19104
Julio Arroyo West Columbia South Carolina 29169
Vanderbilt Univ Med Ctr Nashville Tennessee 37203
Univ of Texas, Southwestern Med Ctr of Dallas Dallas Texas 75390
Univ of Washington Seattle Washington 98104

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 NCT00001132, 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 8, 2008 · Synced Sep 9, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00001132 live on ClinicalTrials.gov.

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