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Completed Phase 2 Interventional

A Study of the Safety and Efficacy of Chronically Administered MDL 28,574A in the Treatment of HIV-Infected Patients

ClinicalTrials.gov ID: NCT00002150

Public ClinicalTrials.gov record NCT00002150. 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 26, 2026, 6:19 PM EDT

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

Brief summary

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

To characterize the safety and efficacy of fixed doses of MDL 28,574A administered alone and in combination with zidovudine ( AZT ) in patients with asymptomatic or mildly symptomatic HIV infection. To examine the demographic effects on population pharmacokinetics and pharmacodynamics of MDL 28,574A alone and in combination with AZT.

Study identification

NCT ID
NCT00002150
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Hoechst Marion Roussel
Industry
Enrollment
200 participants

Conditions and interventions

Conditions

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

United States locations

U.S. sites
23
U.S. states
14
U.S. cities
22
Facility City State ZIP Site status
Clinical Investigations Health Services Mobile Alabama 366880002 —
California Clinical Trials Med Group Beverly Hills California 90211 —
Southwest Community Based AIDS Treatment Group - COMBAT Los Angeles California 90027 —
UCSF - San Francisco Gen Hosp San Francisco California 94110 —
George Washington Univ / Hershey Med Ctr Washington D.C. District of Columbia 20037 —
Community Research Initiative of South Florida Coral Gables Florida 33146 —
Independent Investigator Fort Lauderdale Florida 33316 —
North Broward Hosp District Fort Lauderdale Florida 33316 —
Clinical Research Ctr Sarasota Florida 34239 —
Independent Investigator Vero Beach Florida 32960 —
Ctr for Special Immunology Chicago Illinois 60657 —
Indiana Univ Hosp Indianapolis Indiana 462025250 —
Univ of Kansas School of Medicine Wichita Kansas 67214 —
Univ Health Ctr Detroit Michigan 48201 —
Antibiotic Research Associates Kansas City Missouri 64132 —
North Jersey Community Research Initiative Newark New Jersey 071032842 —
Community Health Network Rochester New York 14620 —
SUNY / Health Sciences Ctr at Stony Brook Stony Brook New York 117948153 —
Infectious Disease Associates Toledo Ohio 43608 —
Guthrie Clinic Sayre Pennsylvania 18840 —
Univ of Texas Southwestern Med Ctr of Dallas Dallas Texas 752359103 —
Univ TX Galveston Med Branch Galveston Texas 775550835 —
Houston Clinical Research Network Houston Texas 77006 —

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 NCT00002150, 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 Sep 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00002150 live on ClinicalTrials.gov.

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