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Randomized, Open-Label, Multiple-Dose Study to Evaluate the Effect of Famotidine on the Pharmacokinetics of Atazanavir/Ritonavir/Tenofovir in Healthy Subjects
The purpose of this clinical research study is to assess the pharmacokinetics of atazanavir, identifying one or more dosing regimens of atazanavir/ritonavir/tenofovir when dosed with famotidine results in atazanavir exposures similar to those when atazanavir/ritonavir/tenofovir 300/100/300 mg is dosed without famotidine in healthy subjects.
Age
18 - 50 years
Sex
ALL
Healthy Volunteers
Yes
Local Institution
Hamilton, New Jersey, United States
Start Date
April 1, 2006
Primary Completion Date
June 1, 2006
Completion Date
June 1, 2006
Last Updated
April 8, 2011
40
Estimated participants
Atazanavir+Ritonavir+Tenofovir
DRUG
Atazanavir+Ritonavir+Tenofovir+Famotidine
DRUG
Atazanavir+Ritonavir+Tenofovir+Famotidine
DRUG
Atazanavir+Ritonavir+Tenofovir+Famotidine
DRUG
Atazanavir+Ritonavir+Tenofovir+Famotidine
DRUG
Lead Sponsor
Bristol-Myers Squibb
NCT04142047
NCT06694805
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