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Completed Phase 3 Interventional

The Safety and Effectiveness of Three Anti-HIV Drug Combinations in HIV-Infected Patients Who Have Taken AZT

ClinicalTrials.gov ID: NCT00002436

Public ClinicalTrials.gov record NCT00002436. 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 Jun 26, 2026, 4:07 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

A Randomized Lamivudine (3TC)/Dideoxycytidine (ddC) Double-Blind Multicenter Trial (With Open-Label AZT) to Evaluate the Safety and Efficacy of Low Dose 3TC Administered Concurrently With AZT Versus High Dose 3TC Administered Concurrently With AZT Versus ddC Administered Concurrently With AZT in the Treatment of HIV-1 Infected, AZT-Experienced (>= 24 Weeks) Patients With CD4 Counts of 100-300 Cells/mm3

Study identification

NCT ID
NCT00002436
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Glaxo Wellcome
Industry
Enrollment
325 participants

Conditions and interventions

Conditions

Interventions

  • Lamivudine Drug
  • Zidovudine Drug
  • Zalcitabine Drug

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
Not listed
Primary completion
Not listed
Completion
Not listed
Last update posted
Jun 23, 2005

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
17
Facility City State ZIP Site status
Combat Group Los Angeles California 90028
San Diego Community Research Group San Diego California 92104
ViRx Inc San Francisco California 94103
AIDS Research Consortium of Atlanta Atlanta Georgia 30308
Chicago Ctr for Clinical Research Chicago Illinois 60607
Louisiana Cardiovascular Research Ctr New Orleans Louisiana 70119
Boston City Hosp / FGH-1 Boston Massachusetts 02118
Nassau County Med Ctr East Meadow New York 11554
Saint Luke's - Roosevelt Hosp Ctr New York New York 10019
Nalle Clinic Charlotte North Carolina 28207
Duke Univ Med Ctr Durham North Carolina 27710
Portland Veterans Adm Med Ctr / Rsch & Education Grp Portland Oregon 97210
Milton S Hershey Med Ctr Hershey Pennsylvania 17033
Central Texas Med Foundation Austin Texas 78751
Univ of Texas Southwestern Med Ctr of Dallas Dallas Texas 75235
Nicholaos Bellos Dallas Texas 75246
Houston Clinical Research Network Houston Texas 77006
Wisconsin Community - Based Research Consortium Milwaukee Wisconsin 53202

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 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00002436, 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 23, 2005 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00002436 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →