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Completed Phase 2 Interventional

The Safety and Effectiveness of Nevirapine and Zidovudine, Given Separately and Together, in HIV-1 Infected Patients Who Have No Symptoms of the Disease

ClinicalTrials.gov ID: NCT00002324

Public ClinicalTrials.gov record NCT00002324. 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 Jul 22, 2026, 3:30 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 Multi-Center, Placebo-Controlled, Double-Blind, Randomized Trial Comparing the Activity, Safety, and Tolerance of 1) 400 Mg Nevirapine in Combination With 500-600 Mg Zidovudine Versus Zidovudine Alone in Asymptomatic HIV-1 Infected Patients With 3-24 Months of Prior Zidovudine Therapy and 200-500 CD4 Cells/mm3 and 2) 400 Mg Nevirapine Versus Nevirapine Placebo in Asymptomatic HIV-1 Nucleoside Naive Patients With 200-500 CD4 Cells/mm3

Study identification

NCT ID
NCT00002324
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
250 participants

Conditions and interventions

Conditions

Interventions

  • Nevirapine Drug
  • Zidovudine Drug

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
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
14
U.S. cities
18
Facility City State ZIP Site status
UCSD Treatment Ctr San Diego California 92103
Saint Francis Mem Hosp San Francisco California 94109
Wilmington Hosp Wilmington Delaware 19801
Community Research Initiative of South Florida Coral Gables Florida 33146
Goodgame Med Group Maitland Florida 32751
Univ of Kansas School of Medicine Wichita Kansas 67214
Chandler Med Ctr Lexington Kentucky 405360084
Kansas City AIDS Research Consortium Kansas City Missouri 641082792
Community Research Initiative on AIDS New York New York 10001
Med College of Ohio Toledo Ohio 43699
Associates Med and Mental Health Tulsa Oklahoma 74114
Philadelphia FIGHT Philadelphia Pennsylvania 19107
Dr Alfred F Burnside Jr Columbia South Carolina 29204
Nelson-Tebedo Community Clinic Dallas Texas 75219
Houston Clinical Research Network Houston Texas 77006
Univ of Utah School of Medicine Salt Lake City Utah 84132
Infectious Disease Physicians Inc Annandale Virginia 22203
Richmond AIDS Consortium Richmond Virginia 23219

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 NCT00002324, 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 Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00002324 live on ClinicalTrials.gov.

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