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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. 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.
Interventions
- DRUG Dexmethylphenidate Hydrochloride
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 24 participants |
| Start Date | 2004-06 |
| Est. Completion | 2004-06 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00829712
The ClinicalTrials.gov registry entry for NCT00829712 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 1 intervention - of which Dexmethylphenidate Hydrochloride is the first listed.
NCT00829712 reports 0 study locations.
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.
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