Drug Interaction Study With Famotidine, Atazanavir, and Atazanavir/Ritonavir/Tenofovir
Completed · Phase 1
Conditions studied: HIV Infections
In brief
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.
Key facts
- Study ID
- NCT00365339
- Run by
- Bristol-Myers Squibb
- People needed
- 40
- Starts
- 2006-04-01
- Expected to finish
- 2006-06-01
- Last updated by the study team
- 2011-04-08
Who can join
Age: 18 and older, up to 50. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy male and female subjects between the ages 18 to 50 years old with a BMI 18 to 32 kg/m2
Where it is running
- Local Institution — Hamilton, New Jersey, United States
Full record on ClinicalTrials.gov
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