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NCT00649441 · ClinicalTrials.gov registry record · Phase 1
Fasting Study of Quinapril HCl and Hydrochlorothiazide Tablets 20 mg/25 mg to Accuretic™ Tablets 20 mg/25 mg
A Phase 1 study, sponsored by Mylan Pharmaceuticals.
- Completed
- Registry status
- Phase 1
- Development phase
- 60
- Enrollment target
NCT00649441 is a Phase 1 study that has completed, run by Mylan Pharmaceuticals. The registered enrollment target is 60 participants.
The verdict
NCT00649441, 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's quinapril HCl and hydrochlorothiazide 20 mg/25 mg tablets to Parke-Davis' Accuretic™ 20 mg/25 mg tablets following a single, oral 20 mg/25 mg (1 x 20 mg/25 mg) dose administered under fasting conditions.
Interventions
- DRUG Quinapril HCl and Hydrochlorothiazide Tablets 20 mg/25 mg
- DRUG Accuretic™ Tablets 20 mg/25 mg
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2003-08 |
| Est. Completion | 2003-09 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00649441
The ClinicalTrials.gov registry entry for NCT00649441 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 HCl and Hydrochlorothiazide Tablets 20 mg/25 mg is the first listed.
NCT00649441 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00649441 about?
NCT00649441 is a clinical study titled "Fasting Study of Quinapril HCl and Hydrochlorothiazide Tablets 20 mg/25 mg to Accuretic™ Tablets 20 mg/25 mg". The objective of this study was to investigate the bioequivalence of Mylan's quinapril HCl and hydrochlorothiazide 20 mg/25 mg tablets to Parke-Davis' Accuretic™ 20 mg/25 mg tablets following a single, oral 20 mg/25 mg (1 x 20 mg/25 mg) dose administered under fasting conditions.
What is the current status of trial NCT00649441?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 60 participants. The study started on 2003-08. Estimated completion is 2003-09.
What interventions are being tested in trial NCT00649441?
The interventions under investigation include: Quinapril HCl and Hydrochlorothiazide Tablets 20 mg/25 mg (DRUG), Accuretic™ Tablets 20 mg/25 mg (DRUG).
Who is sponsoring clinical trial NCT00649441?
This trial is sponsored by Mylan Pharmaceuticals, which has 146 total clinical trials registered on ClinicalTrials.gov.
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