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NCT00365339 · ClinicalTrials.gov registry record · Phase 1
Drug Interaction Study With Famotidine, Atazanavir, and Atazanavir/Ritonavir/Tenofovir
A Phase 1 study, sponsored by Bristol-Myers Squibb.
- Completed
- Registry status
- Phase 1
- Development phase
- 40
- Enrollment target
NCT00365339: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.
NCT00365339 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 40 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00365339, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 40 participants
- Enrollment target
Study Summary
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.
Interventions
- DRUG Atazanavir+Ritonavir+Tenofovir
- DRUG Atazanavir+Ritonavir+Tenofovir+Famotidine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2006-04 |
| Est. Completion | 2006-06 |
| Phase | Phase 1 |
What the finished NCT00365339 record still lists
NCT00365339 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower).
The record links to 0 conditions, and to 2 interventions - of which Atazanavir+Ritonavir+Tenofovir is the first listed.
NCT00365339 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00365339 about?
NCT00365339 is a clinical study titled "Drug Interaction Study With Famotidine, Atazanavir, and Atazanavir/Ritonavir/Tenofovir". 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 dos...
What is the current status of trial NCT00365339?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2006-04. Estimated completion is 2006-06.
What interventions are being tested in trial NCT00365339?
The interventions under investigation include: Atazanavir+Ritonavir+Tenofovir (DRUG), Atazanavir+Ritonavir+Tenofovir+Famotidine (DRUG).
Who is sponsoring clinical trial NCT00365339?
This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00365339's enrollment target sits among peer trials
40 1130th of 2000 higher than 810 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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