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NCT00834990 · ClinicalTrials.gov registry record · Phase 1
Divalproex Sodium Delayed-Release Tablets Under Non-Fasting Conditions
A Phase 1 study, sponsored by Teva Pharmaceuticals USA.
- Completed
- Registry status
- Phase 1
- Development phase
- 24
- Enrollment target
NCT00834990: Completed Phase 1 study, sponsored by Teva Pharmaceuticals USA.
NCT00834990 is a Phase 1 study that has completed, run by Teva Pharmaceuticals USA. The registered enrollment target is 24 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00834990, a Phase 1 study, has completed, sponsored by Teva Pharmaceuticals USA.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 24 participants
- Enrollment target
Study Summary
This study will compare the relative bioavailability of 500 mg Divalproex Sodium Delayed-Release Tablets with that of 500 mg Depakote® Tablets following a single oral dose (1 x 500 mg tablets) in healthy subjects under non-fasting conditions.
Interventions
- DRUG divalproex sodium
- DRUG Depakote®
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 24 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 NCT00834990
The ClinicalTrials.gov registry entry for NCT00834990 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 24 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 divalproex sodium is the first listed.
NCT00834990 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00834990 about?
NCT00834990 is a clinical study titled "Divalproex Sodium Delayed-Release Tablets Under Non-Fasting Conditions". This study will compare the relative bioavailability of 500 mg Divalproex Sodium Delayed-Release Tablets with that of 500 mg Depakote® Tablets following a single oral dose (1 x 500 mg tablets) in healthy subjects under non-fasting conditions.
What is the current status of trial NCT00834990?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2003-09. Estimated completion is 2003-09.
What interventions are being tested in trial NCT00834990?
The interventions under investigation include: divalproex sodium (DRUG), Depakote® (DRUG).
Who is sponsoring clinical trial NCT00834990?
This trial is sponsored by Teva Pharmaceuticals USA, which has 83 total clinical trials registered on ClinicalTrials.gov.
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