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Completed Phase 2 Interventional

Using Drug Levels and Drug Resistance Testing to Select Effective Anti-HIV Drug Combinations in Patients With Drug-resistant HIV

ClinicalTrials.gov ID: NCT00027339

Public ClinicalTrials.gov record NCT00027339. 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 Jul 22, 2026, 11:47 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 Phase II Study of the Predictive Value of Pharmacokinetic-Adjusted Phenotypic Susceptibility (C12h/IC50) on Antiretroviral Response to Ritonavir-Enhanced Protease Inhibitors in Subjects With Failure of Previous Protease Inhibitor-Based Regimens

Study identification

NCT ID
NCT00027339
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
NIH
Enrollment
53 participants

Conditions and interventions

Conditions

Interventions

  • lopinavir/ritonavir Drug
  • indinavir sulfate Drug
  • tenofovir disoproxil fumarate Drug
  • ritonavir Drug
  • fosamprenavir Drug

Drug

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
May 31, 2005
Last update posted
Oct 31, 2021

Ends 2005

United States locations

U.S. sites
13
U.S. states
7
U.S. cities
11
Facility City State ZIP Site status
USC CRS Los Angeles California
Stanford CRS Palo Alto California 94305-5107
UC Davis Medical Center Sacramento California 95814
Ucsd, Avrc Crs San Diego California 92103
University of Colorado Hospital CRS Aurora Colorado 80262
Univ. of Miami AIDS CRS Miami Florida
Indiana Univ. School of Medicine, Wishard Memorial Indianapolis Indiana 46202
Methodist Hosp. of Indiana Indianapolis Indiana 46202
Beth Israel Med. Ctr., ACTU New York New York 10003
NY Univ. HIV/AIDS CRS New York New York 10016
Unc Aids Crs Chapel Hill North Carolina 275997215
Duke Univ. Med. Ctr. Adult CRS Durham North Carolina 27710
Vanderbilt Therapeutics CRS Nashville Tennessee 37203

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 NCT00027339, 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 31, 2021 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00027339 live on ClinicalTrials.gov.

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