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NCT00859430 · ClinicalTrials.gov registry record · Phase 1
Levetiracetam 1000 mg Under Non-Fasting Conditions
A Phase 1 study, sponsored by Teva Pharmaceuticals USA.
- Completed
- Registry status
- Phase 1
- Development phase
- 22
- Enrollment target
NCT00859430: Completed Phase 1 study, sponsored by Teva Pharmaceuticals USA.
NCT00859430 is a Phase 1 study that has completed, run by Teva Pharmaceuticals USA. The registered enrollment target is 22 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (63% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00859430, a Phase 1 study, has completed, sponsored by Teva Pharmaceuticals USA.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 22 participants
- Enrollment target
Study Summary
The objective of this study is to compare the rate and extent of absorption of an investigational formulation of levetiracetam 1000 mg tablet to an equivalent oral dose of the commercially available reference product under fed conditions.
Primary Outcome
Bioequivalence based on Cmax
Interventions
- DRUG Levetiracetam
- DRUG Keppra®
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 22 participants |
| Start Date | 2007-01 |
| Est. Completion | 2007-01 |
| Phase | Phase 1 |
What the finished NCT00859430 record still lists
NCT00859430 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 22 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (63% lower).
The record links to 0 conditions, and to 2 interventions - of which Levetiracetam is the first listed.
NCT00859430 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00859430 about?
NCT00859430 is a clinical study titled "Levetiracetam 1000 mg Under Non-Fasting Conditions". The objective of this study is to compare the rate and extent of absorption of an investigational formulation of levetiracetam 1000 mg tablet to an equivalent oral dose of the commercially available reference product under fed conditions.
What is the current status of trial NCT00859430?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 22 participants. The study started on 2007-01. Estimated completion is 2007-01.
What interventions are being tested in trial NCT00859430?
The interventions under investigation include: Levetiracetam (DRUG), Keppra® (DRUG).
Who is sponsoring clinical trial NCT00859430?
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 NCT00859430's enrollment target sits among peer trials
22 1601st of 2000 higher than 386 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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