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NCT00649103 · ClinicalTrials.gov registry record · Phase 1
Fasting Study of Quinapril Hydrochloride Tablets 40 mg and Accupril® Tablets 40 mg
A Phase 1 study, sponsored by Mylan Pharmaceuticals.
- Completed
- Registry status
- Phase 1
- Development phase
- 60
- Enrollment target
NCT00649103 is a Phase 1 study that has completed, run by Mylan Pharmaceuticals. The registered enrollment target is 60 participants.
The verdict
NCT00649103, a Phase 1 study, has completed, sponsored by Mylan Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 60 participants
- Enrollment target
Study Summary
The objective of this study was to investigate the bioequivalence of Mylan quinapril hydrochloride 40 mg tablets compared to Parke-Davis Accupril® 40 mg tablets following a single, oral 40 mg (1 x 40 mg) dose under fasting conditions.
Interventions
- DRUG Quinapril Hydrochloride Tablets 40 mg
- DRUG Accupril® Tablets 40 mg
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2002-12 |
| Est. Completion | 2003-01 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00649103
The ClinicalTrials.gov registry entry for NCT00649103 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Mylan Pharmaceuticals, which has 146 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Quinapril Hydrochloride Tablets 40 mg is the first listed.
NCT00649103 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00649103 about?
NCT00649103 is a clinical study titled "Fasting Study of Quinapril Hydrochloride Tablets 40 mg and Accupril® Tablets 40 mg". The objective of this study was to investigate the bioequivalence of Mylan quinapril hydrochloride 40 mg tablets compared to Parke-Davis Accupril® 40 mg tablets following a single, oral 40 mg (1 x 40 mg) dose under fasting conditions.
What is the current status of trial NCT00649103?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 60 participants. The study started on 2002-12. Estimated completion is 2003-01.
What interventions are being tested in trial NCT00649103?
The interventions under investigation include: Quinapril Hydrochloride Tablets 40 mg (DRUG), Accupril® Tablets 40 mg (DRUG).
Who is sponsoring clinical trial NCT00649103?
This trial is sponsored by Mylan Pharmaceuticals, which has 146 total clinical trials registered on ClinicalTrials.gov.
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