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Not listed Phase 2 Interventional

Safety and Effectiveness of an Anti-HIV Drug Combination Taken Twice Daily

ClinicalTrials.gov ID: NCT00002241

Public ClinicalTrials.gov record NCT00002241. 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 7, 2026, 2:48 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 Multicenter, Open-Label, 24-Week Pilot Study to Evaluate the Safety and Efficacy of Indinavir Sulfate 800 Mg b.i.d. in Combination With Ritonavir 100 Mg/d4T/3TC b.i.d. in HIV-Infected Individuals

Brief summary

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

The purpose of this study is to see whether taking indinavir (IDV) plus ritonavir (RTV) plus stavudine (d4T) plus lamivudine (3TC) 2 times each day is safe and can lower the level of HIV in the blood.

Study identification

NCT ID
NCT00002241
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Enrollment
80 participants

Conditions and interventions

Conditions

Interventions

Drug

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
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
9
U.S. cities
12
Facility City State ZIP Site status
Univ of Alabama at Birmingham Birmingham Alabama 35294
Apogee Med Group San Diego California 92101
Univ of California at San Francisco Gen Hosp San Francisco California 94110
HIV Institute / Davies Med Ctr San Francisco California 94114
Kaiser Foundation Hospital San Francisco California 94118
Univ of Miami School of Medicine Miami Florida 33136
AIDS Research Alliance - Chicago Chicago Illinois 60657
Tulane Univ School of Medicine New Orleans Louisiana 70112
CRI New England Brookline Massachusetts 02146
SUNY Health Sciences Ctr Brooklyn New York 11203
Chelsea Village Med Ctr New York New York 10014
Liberty Med Group New York New York 10016
St Lukes / Roosevelt Hosp / HIV Center New York New York 10019
Mount Sinai Med Ctr New York New York 10029
Bronx Lebanon Hosp Ctr The Bronx New York 10456
Montefiore Med Ctr The Bronx New York 10467
Mark Watkins Philadelphia Pennsylvania 19107
Univ of Texas / Thomas Street Clinic Houston Texas 77030

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 NCT00002241, 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 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00002241 live on ClinicalTrials.gov.

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