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NCT00648050 · ClinicalTrials.gov registry record · Phase 1
Fasting Study of Verapamil HCl Extended-Release Capsules 300 mg to Verelan® PM Extended-Release Capsules 300 mg
A Phase 1 study, sponsored by Mylan Pharmaceuticals.
- Completed
- Registry status
- Phase 1
- Development phase
- 72
- Enrollment target
NCT00648050: Completed Phase 1 study, sponsored by Mylan Pharmaceuticals.
NCT00648050 is a Phase 1 study that has completed, run by Mylan Pharmaceuticals. The registered enrollment target is 72 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (20% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00648050, a Phase 1 study, has completed, sponsored by Mylan Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 72 participants
- Enrollment target
Study Summary
The objective for this study was to investigate the bioequivalence of Mylan's verapamil HCl extended-release 300 mg capsules to Schwarz's Verelan® PM extended-release 300 mg capsules following evening administration of a single, oral 300 mg (1 x 300 mg) dose administration under fasting conditions.
Interventions
- DRUG Verapamil Hydrochloride Extended-Release Capsules, 300 mg
- DRUG Verelan® PM Extended-Release Capsules, 300 mg
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 72 participants |
| Start Date | 2006-03 |
| Est. Completion | 2006-03 |
| Phase | Phase 1 |
What the finished NCT00648050 record still lists
NCT00648050 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 72 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (20% higher).
The record links to 0 conditions, and to 2 interventions - of which Verapamil Hydrochloride Extended-Release Capsules, 300 mg is the first listed.
NCT00648050 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00648050 about?
NCT00648050 is a clinical study titled "Fasting Study of Verapamil HCl Extended-Release Capsules 300 mg to Verelan® PM Extended-Release Capsules 300 mg". The objective for this study was to investigate the bioequivalence of Mylan's verapamil HCl extended-release 300 mg capsules to Schwarz's Verelan® PM extended-release 300 mg capsules following evening administration of a single, oral 300 mg (1 x 300 mg) dose administration under fasting conditions.
What is the current status of trial NCT00648050?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 72 participants. The study started on 2006-03. Estimated completion is 2006-03.
What interventions are being tested in trial NCT00648050?
The interventions under investigation include: Verapamil Hydrochloride Extended-Release Capsules, 300 mg (DRUG), Verelan® PM Extended-Release Capsules, 300 mg (DRUG).
Who is sponsoring clinical trial NCT00648050?
This trial is sponsored by Mylan Pharmaceuticals, which has 146 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00648050's enrollment target sits among peer trials
72 736th of 2000 higher than 1,254 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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