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NCT00840281 · ClinicalTrials.gov registry record · Phase 1
Cefprozil 500 mg Tablets Under Fasting Conditions
A Phase 1 study, sponsored by Teva Pharmaceuticals USA.
- Completed
- Registry status
- Phase 1
- Development phase
- 38
- Enrollment target
NCT00840281: Completed Phase 1 study, sponsored by Teva Pharmaceuticals USA.
NCT00840281 is a Phase 1 study that has completed, run by Teva Pharmaceuticals USA. The registered enrollment target is 38 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00840281, a Phase 1 study, has completed, sponsored by Teva Pharmaceuticals USA.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 38 participants
- Enrollment target
Study Summary
The objective of this study is to compare the relative bioavailability of cefprozil 500 mg tablets (Teva Pharmaceuticals USA) with that of Cefzil® 500 mg tablets (Bristol-Myers Squibb) in healthy, non-smoking adults under fasting conditions.
Interventions
- DRUG Cefzil® 500 mg tablets
- DRUG Cefprozil 500 mg Tablets
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 38 participants |
| Start Date | 2003-09 |
| Est. Completion | 2003-09 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00840281
The ClinicalTrials.gov registry entry for NCT00840281 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 38 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Teva Pharmaceuticals USA, which has 83 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Cefzil® 500 mg tablets is the first listed.
NCT00840281 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00840281 about?
NCT00840281 is a clinical study titled "Cefprozil 500 mg Tablets Under Fasting Conditions". The objective of this study is to compare the relative bioavailability of cefprozil 500 mg tablets (Teva Pharmaceuticals USA) with that of Cefzil® 500 mg tablets (Bristol-Myers Squibb) in healthy, non-smoking adults under fasting conditions.
What is the current status of trial NCT00840281?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 38 participants. The study started on 2003-09. Estimated completion is 2003-09.
What interventions are being tested in trial NCT00840281?
The interventions under investigation include: Cefzil® 500 mg tablets (DRUG), Cefprozil 500 mg Tablets (DRUG).
Who is sponsoring clinical trial NCT00840281?
This trial is sponsored by Teva Pharmaceuticals USA, which has 83 total clinical trials registered on ClinicalTrials.gov.
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