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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 Oct 24, 2026, 4:24 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 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 24, 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 24, 2005 · Synced Oct 24, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00002241 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →