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NCT00840866 · ClinicalTrials.gov registry record · Phase 1
Cefprozil 500 mg Tablets Under Fed Conditions
A Phase 1 study, sponsored by Teva Pharmaceuticals USA.
- Completed
- Registry status
- Phase 1
- Development phase
- 39
- Enrollment target
NCT00840866: Completed Phase 1 study, sponsored by Teva Pharmaceuticals USA.
NCT00840866 is a Phase 1 study that has completed, run by Teva Pharmaceuticals USA. The registered enrollment target is 39 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (35% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00840866, a Phase 1 study, has completed, sponsored by Teva Pharmaceuticals USA.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 39 participants
- Enrollment target
Study Summary
The objective of this study is to compare the relative bioavailability of cefprozil 500 mg tablets with that of Cefzil 500 mg tablets in healthy, non-smoking adults under non-fasting conditions.
Primary Outcome
Bioequivalence based on Cmax.
Interventions
- DRUG cefprozil
- DRUG Cefzil®
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 39 participants |
| Start Date | 2003-09 |
| Est. Completion | 2003-09 |
| Phase | Phase 1 |
What the finished NCT00840866 record still lists
NCT00840866 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 39 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (35% lower).
The record links to 0 conditions, and to 2 interventions - of which cefprozil is the first listed.
NCT00840866 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00840866 about?
NCT00840866 is a clinical study titled "Cefprozil 500 mg Tablets Under Fed Conditions". The objective of this study is to compare the relative bioavailability of cefprozil 500 mg tablets with that of Cefzil 500 mg tablets in healthy, non-smoking adults under non-fasting conditions.
What is the current status of trial NCT00840866?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 39 participants. The study started on 2003-09. Estimated completion is 2003-09.
What interventions are being tested in trial NCT00840866?
The interventions under investigation include: cefprozil (DRUG), Cefzil® (DRUG).
Who is sponsoring clinical trial NCT00840866?
This trial is sponsored by Teva Pharmaceuticals USA, which has 83 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00840866's enrollment target sits among peer trials
39 1191st of 2000 higher than 804 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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