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Completed Phase 2 Interventional

Phase 2 Safety and Efficacy Study of Bevirimat Functional Monotherapy in HIV Treatment-Experienced Patients for 2 Weeks*

ClinicalTrials.gov ID: NCT00511368

Public ClinicalTrials.gov record NCT00511368. 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 23, 2026, 11:02 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

Phase 2 Dose-escalating, P-C, D-B, Parallel Group Study in HIV Treatment-experienced Patients to Evaluate the Safety, Tolerability and Efficacy of PA103001-04 Administered as Functional Monotherapy for 14 Days *(PART B)

Study identification

NCT ID
NCT00511368
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Myrexis Inc.
Industry
Enrollment
92 participants

Conditions and interventions

Conditions

Interventions

  • matching placebo Drug
  • Bevirimat Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
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
Mar 31, 2006
Primary completion
Jun 30, 2008
Completion
Jun 30, 2008
Last update posted
Jan 19, 2010

2006 – 2008

United States locations

U.S. sites
18
U.S. states
12
U.S. cities
17
Facility City State ZIP Site status
UCLA Medical Center Los Angeles California 90035
Quest Clinical Research San Francisco California 94115
University of Colorado Health Science Center Denver Colorado 80262
George Washington University Medical Center Washington D.C. District of Columbia 20037
Whitman-Walker Clinic Washington D.C. District of Columbia 20037
Gary Richmond Fort Lauderdale Florida 33316
Orlando Immunology Center Orlando Florida 32803
AIDS Research Consortium of Atlanta, Inc. Atlanta Georgia 30308
Northwestern University Feinberg School of Medicine Chicago Illinois 60611
The Research Insitute Boston Massachusetts 02215
UNC at Chapel Hill Chapel Hill North Carolina 27599
University Hospitals of Cleveland Cleveland Ohio 44106
Ohio State University Medical Center Columbus Ohio 43210
Drexel University College of Medicine Philadelphia Pennsylvania 19102
Miriam Hospital/Brown University Providence Rhode Island 02906
Central Texas Clinical Research Austin Texas 78705
Southwest Infectious Diseases Dallas Texas 75204
University of Texas Medical Branch Internal Medicine Galveston Texas 77210-4786

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 NCT00511368, 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 Jan 19, 2010 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00511368 live on ClinicalTrials.gov.

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