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A Phase IV, Multicenter, Cross-sectional Study to Evaluate the I50L Substitution Among Subjects Experiencing Virologic Failure on a HAART Regimen Containing Atazanavir (ATV)
The purpose of this study is to find out the frequency of the I50L substitution among patients experiencing treatment failure on an atazanavir-containing regimen.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Local Institution
Phoenix, Arizona, United States
Vista Medical Partners
Beverly Hills, California, United States
AIDS Healthcare Foundation
Beverly Hills, California, United States
AltaMed Health Services Corporation
Los Angeles, California, United States
Kaiser Permanente
Los Angeles, California, United States
Synergy Hematology and Oncology Medical Associates
Los Angeles, California, United States
Orange Coast Medical Group
Newport Beach, California, United States
Alameda County Medical Center
Oakland, California, United States
East Bay AIDS Center
Oakland, California, United States
Desert Medical Group
Palm Springs, California, United States
Start Date
September 1, 2004
Primary Completion Date
September 1, 2009
Completion Date
September 1, 2009
Last Updated
April 14, 2011
5,000
ESTIMATED participants
Lead Sponsor
Bristol-Myers Squibb
NCT06694805
NCT04142047
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07428330