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Completed Phase 2 Interventional

Study of a New Protease Inhibitor, BMS-232632, in Combination With Other Anti-HIV Drugs

ClinicalTrials.gov ID: NCT00002240

Public ClinicalTrials.gov record NCT00002240. 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 19, 2026, 6:35 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

Evaluation of the Safety and Antiviral Efficacy of a Novel HIV-1 Protease Inhibitor, BMS-232632, Alone and in Combination With d4T and ddI as Compared to a Reference Combination Regimen

Brief summary

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

The purpose of this study is to evaluate a new protease inhibitor known as BMS-232632. This drug will be given in combination with 2 other anti-HIV drugs (stavudine and didanosine). The effectiveness of BMS-232632 against HIV infection will be compared to that of nelfinavir, a protease inhibitor that is already commonly prescribed.

Study identification

NCT ID
NCT00002240
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
Not listed

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 1999 (Type not available)
Primary completion
Dec 2001 (Actual)
Completion
Dec 2001 (Actual)
Last update posted
May 4, 2011

1999 – 2001

United States locations

U.S. sites
16
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
Clinsites / Sorra Research Ctr Birmingham Alabama 35203 —
Univ of Alabama at Birmingham Birmingham Alabama 35294 —
UCSD Treatment Ctr San Diego California 92103 —
UCSF - San Francisco Gen Hosp San Francisco California 94110 —
Univ of Colorado / Health Science Ctr Denver Colorado 80262 —
ViRx / Dupont Circle Physicians Group Washington D.C. District of Columbia 20009 —
AIDS Research Consortium of Atlanta Atlanta Georgia 30308 —
Rush Presbyterian - Saint Luke's Med Ctr Chicago Illinois 60612 —
Washington Univ School of Medicine St Louis Missouri 63108 —
Albany Med College Albany New York 12208 —
Beth Israel Med Ctr New York New York 10003 —
Columbia Presbyterian Med Ctr New York New York 10032 —
Case Western Reserve Univ Cleveland Ohio 44106 —
Oak Lawn Physicians Group Dallas Texas 75219 —
Univ of Texas Southwestern Med Ctr of Dallas Dallas Texas 75235 —
Univ TX Galveston Med Branch Galveston Texas 77555 —

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 NCT00002240, 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 May 4, 2011 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00002240 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →