Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional

A Study to Compare Three Doses of T-20 When Given in Combination With Abacavir, Amprenavir, Ritonavir, and Efavirenz to HIV-Infected Adults

ClinicalTrials.gov ID: NCT00002239

Public ClinicalTrials.gov record NCT00002239. 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 26, 2026, 11:07 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 Controlled Phase 2 Trial Assessing Three Doses of T-20 in Combination With Abacavir, Amprenavir, Ritonavir, and Efavirenz in HIV-1 Infected Adults

Brief summary

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

The purpose of this study is to see if it is safe and effective to give T-20, a new type of anti-HIV drug, with a combination of other anti-HIV drugs. The other anti-HIV drugs used are abacavir (ABC), amprenavir (APV), ritonavir (RTV), and efavirenz (EFV). Three different doses of T-20 are tested.

Study identification

NCT ID
NCT00002239
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
68 participants

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
May 1999 (Type not available)
Primary completion
Not listed
Completion
Not listed
Last update posted
Nov 15, 2005

Started 1999

United States locations

U.S. sites
20
U.S. states
11
U.S. cities
17
Facility City State ZIP Site status
Pacific Oaks Research Beverly Hills California 90211 —
UCLA Care Ctr Los Angeles California 90095 —
ViRx Inc Palm Springs California 92262 —
Donald Northfelt Palm Springs California 92270 —
UCSD San Diego California 92103 —
ViRx Inc San Francisco California 94109 —
Quest Clinical Research San Francisco California 94115 —
Dupont Circle Physicians Group Washington D.C. District of Columbia 200091104 —
IDC Research Initiative Altamonte Springs Florida 32701 —
Gary Richmond MD Fort Lauderdale Florida 33316 —
AIDS Research Consortium of Atlanta Atlanta Georgia 30308 —
Johns Hopkins Hosp Baltimore Maryland 21287 —
Washington Univ School of Medicine St Louis Missouri 63110 —
New York Univ Med Ctr New York New York 10016 —
Trimeris Inc Durham North Carolina 27707 —
Associates of Med and Mental Health Tulsa Oklahoma 74114 —
Pennsylvania Oncology and Hematology Associates Philadelphia Pennsylvania 19106 —
Philadelphia FIGHT Philadelphia Pennsylvania 19107 —
Univ of Pittsburgh Pittsburgh Pennsylvania 15261 —
Central Texas Clinical Research Austin Texas 78705 —

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 NCT00002239, 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 Nov 15, 2005 · Synced Oct 26, 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 NCT00002239 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →