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Completed Phase 2 Interventional

A Study on Amprenavir in Combination With Other Anti-HIV Drugs in HIV-Positive Patients

ClinicalTrials.gov ID: NCT00000912

Public ClinicalTrials.gov record NCT00000912. 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 2, 2026, 11:40 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 Phase II, Randomized Trial of Amprenavir as Part of Dual Protease Inhibitor Regimens (Placebo-Controlled) in Combination With Abacavir, Efavirenz, and Adefovir Dipivoxil Versus Amprenavir Alone in HIV-Infected Subjects With Prior Exposure to Approved Protease Inhibitors and Loss of Virologic Suppression as Reflected by a Plasma HIV-1 RNA Concentration >= 1,000 Copies/ml

Brief summary

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

The purpose of this study is to compare 4 different combinations of anti-HIV drugs and to determine the number of people whose HIV blood levels decrease to 200 copies/ml or less while on the treatment. This study evaluates the safety of these drug combinations, which include an experimental protease inhibitor (PI), amprenavir. Despite the success that many patients have had with PI treatment regimens, there is still a possibility that patients receiving PIs may continue to have high HIV blood levels. Because of this possibility, alternative drug combinations containing PIs are being studied. It appears that amprenavir, when taken with 3 or 4 other anti-HIV drugs, may be effective in patients with prior PI treatment experience.

Study identification

NCT ID
NCT00000912
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
475 participants

Conditions and interventions

Eligibility (public fields only)

Age range
13 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
Apr 30, 2000
Last update posted
Oct 28, 2021

Ends 2000

United States locations

U.S. sites
44
U.S. states
18
U.S. cities
30
Facility City State ZIP Site status
Univ of Southern California / LA County USC Med Ctr Los Angeles California 900331079
USC Univ Hosp & Ambulatory Hlth Care Ctr / USC Med Ctr Los Angeles California 900334508
UCLA CARE Ctr Los Angeles California 90095
Willow Clinic Menlo Park California 94025
Univ of California / San Diego Treatment Ctr San Diego California 921036325
San Francisco AIDS Clinic / San Francisco Gen Hosp San Francisco California 941102859
San Francisco Gen Hosp San Francisco California 941102859
Santa Clara Valley Med Ctr / AIDS Community Rsch Consortium San Jose California 951282699
San Mateo AIDS Program / Stanford Univ Stanford California 943055107
Stanford Univ Med Ctr Stanford California 943055107
Univ of Colorado Health Sciences Ctr Denver Colorado 80262
Howard Univ Washington D.C. District of Columbia 20059
Univ of Miami School of Medicine Miami Florida 331361013
Emory Univ Atlanta Georgia 30308
Emory Hemo Comp Evaluation Clinic / East TN Comp Hemo Ctr Atlanta Georgia 303652225
Queens Med Ctr Honolulu Hawaii 96816
Univ of Hawaii Honolulu Hawaii 96816
Tripler Army Med Ctr Tripler AMC Hawaii 96859
Northwestern Univ Med School Chicago Illinois 60611
Cook County Hosp Chicago Illinois 60612
Rush Presbyterian - Saint Luke's Med Ctr Chicago Illinois 60612
Charity Hosp / Tulane Univ Med School New Orleans Louisiana 70112
Tulane Univ School of Medicine New Orleans Louisiana 70112
Johns Hopkins Hosp Baltimore Maryland 21287
Harvard (Massachusetts Gen Hosp) Boston Massachusetts 02114
Boston Med Ctr Boston Massachusetts 02118
Univ of Minnesota Minneapolis Minnesota 55455
St Louis Regional Hosp / St Louis Regional Med Ctr St Louis Missouri 63112
SUNY / Erie County Med Ctr at Buffalo Buffalo New York 14215
Bellevue Hosp / New York Univ Med Ctr New York New York 10016
Chelsea Ctr New York New York 10021
Cornell Univ Med Ctr New York New York 10021
Mem Sloan - Kettering Cancer Ctr New York New York 10021
Mount Sinai Med Ctr New York New York 10029
Univ of Rochester Medical Center Rochester New York 14642
Duke Univ Med Ctr Durham North Carolina 27710
Moses H Cone Memorial Hosp Greensboro North Carolina 27401
Univ of Cincinnati Cincinnati Ohio 452670405
Ohio State Univ Hosp Clinic Columbus Ohio 432101228
Milton S Hershey Med Ctr Hershey Pennsylvania 170330850
Univ of Pennsylvania at Philadelphia Philadelphia Pennsylvania 19104
Univ of Pittsburgh Med Ctr Pittsburgh Pennsylvania 15213
Univ of Texas Galveston Galveston Texas 775550435
Univ of Washington Seattle Washington 981224304

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 NCT00000912, 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 Oct 28, 2021 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00000912 live on ClinicalTrials.gov.

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