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NCT00829712 · ClinicalTrials.gov registry record · Phase 1
Dexmethylphenidate Hydrochloride Tablets Under Fasting Conditions
A Phase 1 study, sponsored by Teva Pharmaceuticals USA.
- Completed
- Registry status
- Phase 1
- Development phase
- 24
- Enrollment target
NCT00829712: Completed Phase 1 study, sponsored by Teva Pharmaceuticals USA.
NCT00829712 is a Phase 1 study that has completed, run by Teva Pharmaceuticals USA. The registered enrollment target is 24 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (60% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00829712, a Phase 1 study, has completed, sponsored by Teva Pharmaceuticals USA.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 24 participants
- Enrollment target
Study Summary
The objective of this randomized, single-dose, two-way evaluation is to compare the bioequivalence of a test dexmethylphenidate hydrochloride formulation to an equivalent oral dose of the commercially available dexmethylphenidate hydrochloride in a test population of 24 adult subjects under fasted conditions.
Primary Outcome
Bioequivalence based on Cmax.
Interventions
- DRUG Dexmethylphenidate Hydrochloride
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 24 participants |
| Start Date | 2004-06 |
| Est. Completion | 2004-06 |
| Phase | Phase 1 |
What the finished NCT00829712 record still lists
NCT00829712 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (60% lower).
The record links to 0 conditions, and to 1 intervention - of which Dexmethylphenidate Hydrochloride is the first listed.
NCT00829712 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00829712 about?
NCT00829712 is a clinical study titled "Dexmethylphenidate Hydrochloride Tablets Under Fasting Conditions". The objective of this randomized, single-dose, two-way evaluation is to compare the bioequivalence of a test dexmethylphenidate hydrochloride formulation to an equivalent oral dose of the commercially available dexmethylphenidate hydrochloride in a test population of 24 adult subjects under fasted c...
What is the current status of trial NCT00829712?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2004-06. Estimated completion is 2004-06.
What interventions are being tested in trial NCT00829712?
The interventions under investigation include: Dexmethylphenidate Hydrochloride (DRUG).
Who is sponsoring clinical trial NCT00829712?
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 NCT00829712's enrollment target sits among peer trials
24 1520th of 2000 higher than 405 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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