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Completed Phase 3 Interventional Results available

Atazanavir (BMS-232632) in Combination With Ritonavir or Saquinavir, and Lopinavir/Ritonavir, Each With Tenofovir and a Nucleoside in Subjects With HIV

ClinicalTrials.gov ID: NCT00035932

Public ClinicalTrials.gov record NCT00035932. 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 11, 2026, 5:13 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

Phase III Open Label Atazanavir (BMS-232632) in Combination With Ritonavir or Saquinavir, and Lopinavir/Ritonavir, Each With Tenofovir and a Nucleoside in Subjects With HIV

Brief summary

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

The purpose of this study is to learn how well atazanavir (ATV) works in combination with ritonavir (RTV) or saquinavir (SQV) with tenofovir (TDF) and a nucleoside to reduce the viral load of treatment experienced subjects with human immunodeficiency virus (HIV). There is a comparison arm with lopinavir (LPV)/RTV and TDF and a nucleoside.

Study identification

NCT ID
NCT00035932
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
571 participants

Conditions and interventions

Eligibility (public fields only)

Age range
16 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, 2001
Primary completion
Jun 30, 2003
Completion
Feb 28, 2009
Last update posted
Dec 23, 2010

2001 – 2009

United States locations

U.S. sites
29
U.S. states
15
U.S. cities
26
Facility City State ZIP Site status
Not listed San Francisco California 94121
Not listed Torrance California 90502
Not listed Boulder Colorado 80304
Not listed Altamonte Springs Florida
Not listed Fort Lauderdale Florida 33306
Not listed Fort Lauderdale Florida 33308
Not listed Miami Beach Florida 33160
Not listed Orlando Florida 32801
Not listed Decatur Georgia
Not listed Honolulu Hawaii 96816
Not listed Boise Indiana
Not listed Wichita Kansas 67214
Not listed Louisville Kentucky 40202
Not listed New Orleans Louisiana
Not listed Brookline Massachusetts
Not listed Fall River Massachusetts 02720
Not listed East Orange New Jersey
Not listed Newark New Jersey 07103
Not listed Buffalo New York 14215
Not listed Manhasset New York 11030
Not listed New York New York 10019
Not listed Rochester New York 14620
Not listed Huntersville North Carolina 28078
Not listed Winston-Salem North Carolina 27157
Not listed Winston-Salem North Carolina 29203
Not listed Akron Ohio
Not listed Dallas Texas 75246
Not listed Dallas Texas
Not listed 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 NCT00035932, 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 Dec 23, 2010 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00035932 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →