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NCT00751556 · ClinicalTrials.gov registry record · Phase 1
Single/Multiple Dose Bioavailability Trial
A Phase 1 study, sponsored by Bayer.
- Completed
- Registry status
- Phase 1
- Development phase
- 32
- Enrollment target
NCT00751556: Completed Phase 1 study, sponsored by Bayer.
NCT00751556 is a Phase 1 study that has completed, run by Bayer. The registered enrollment target is 32 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00751556, a Phase 1 study, has completed, sponsored by Bayer.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 32 participants
- Enrollment target
Study Summary
To determine the pharmacokinetic profile of an extended release tablet of naproxen sodium 660 mg relative to the established commercial Aleve 220 mg tablet following single dose administration and at steady-state following multiple dose administration for 4 days.
Interventions
- DRUG Naproxen Sodium 660mg
- DRUG Commercial Aleve 220 mg
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 32 participants |
| Start Date | 2008-02 |
| Est. Completion | 2008-03 |
| Phase | Phase 1 |
What the finished NCT00751556 record still lists
NCT00751556 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower).
The record links to 0 conditions, and to 2 interventions - of which Naproxen Sodium 660mg is the first listed.
NCT00751556 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00751556 about?
NCT00751556 is a clinical study titled "Single/Multiple Dose Bioavailability Trial". To determine the pharmacokinetic profile of an extended release tablet of naproxen sodium 660 mg relative to the established commercial Aleve 220 mg tablet following single dose administration and at steady-state following multiple dose administration for 4 days.
What is the current status of trial NCT00751556?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 32 participants. The study started on 2008-02. Estimated completion is 2008-03.
What interventions are being tested in trial NCT00751556?
The interventions under investigation include: Naproxen Sodium 660mg (DRUG), Commercial Aleve 220 mg (DRUG).
Who is sponsoring clinical trial NCT00751556?
This trial is sponsored by Bayer, which has 591 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00751556's enrollment target sits among peer trials
32 1296th of 2000 higher than 679 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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