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NCT00648570 · ClinicalTrials.gov registry record · Phase 1
Fasting Study of Escitalopram Oxalate Tablets 20 mg and Lexapro® Tablets 20 mg
A Phase 1 study, sponsored by Mylan Pharmaceuticals.
- Completed
- Registry status
- Phase 1
- Development phase
- 37
- Enrollment target
NCT00648570 is a Phase 1 study that has completed, run by Mylan Pharmaceuticals. The registered enrollment target is 37 participants.
The verdict
NCT00648570, a Phase 1 study, has completed, sponsored by Mylan Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 37 participants
- Enrollment target
Study Summary
The objective of this study was to investigate the bioequivalence of Mylan's escitalopram oxalate 20 mg tablets to Forest's Lexapro® 20 mg tablets following a single, oral 20 mg (1 x 20 mg) dose administered under fasting conditions.
Interventions
- DRUG Escitalopram Oxalate Tablets 20 mg
- DRUG Lexapro® Tablets (20 mg
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 37 participants |
| Start Date | 2004-08 |
| Est. Completion | 2004-10 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00648570
The ClinicalTrials.gov registry entry for NCT00648570 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 37 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 Escitalopram Oxalate Tablets 20 mg is the first listed.
NCT00648570 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00648570 about?
NCT00648570 is a clinical study titled "Fasting Study of Escitalopram Oxalate Tablets 20 mg and Lexapro® Tablets 20 mg". The objective of this study was to investigate the bioequivalence of Mylan's escitalopram oxalate 20 mg tablets to Forest's Lexapro® 20 mg tablets following a single, oral 20 mg (1 x 20 mg) dose administered under fasting conditions.
What is the current status of trial NCT00648570?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 37 participants. The study started on 2004-08. Estimated completion is 2004-10.
What interventions are being tested in trial NCT00648570?
The interventions under investigation include: Escitalopram Oxalate Tablets 20 mg (DRUG), Lexapro® Tablets (20 mg (DRUG).
Who is sponsoring clinical trial NCT00648570?
This trial is sponsored by Mylan Pharmaceuticals, which has 146 total clinical trials registered on ClinicalTrials.gov.
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