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NCT00648661 · ClinicalTrials.gov registry record · Phase 1
Food Study of Escitalopram Oxalate Tablets 20 mg to Lexapro® Tablets 20 mg
A Phase 1 study, sponsored by Mylan Pharmaceuticals.
- Completed
- Registry status
- Phase 1
- Development phase
- 35
- Enrollment target
NCT00648661 is a Phase 1 study that has completed, run by Mylan Pharmaceuticals. The registered enrollment target is 35 participants.
The verdict
NCT00648661, a Phase 1 study, has completed, sponsored by Mylan Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 35 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 fed conditions.
Interventions
- DRUG Escitalopram Oxalate Tablets 20 mg
- DRUG Lexapro® Tablets 20 mg
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 35 participants |
| Start Date | 2004-09 |
| Est. Completion | 2004-10 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00648661
The ClinicalTrials.gov registry entry for NCT00648661 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 35 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.
NCT00648661 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00648661 about?
NCT00648661 is a clinical study titled "Food Study of Escitalopram Oxalate Tablets 20 mg to 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 fed conditions.
What is the current status of trial NCT00648661?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 35 participants. The study started on 2004-09. Estimated completion is 2004-10.
What interventions are being tested in trial NCT00648661?
The interventions under investigation include: Escitalopram Oxalate Tablets 20 mg (DRUG), Lexapro® Tablets 20 mg (DRUG).
Who is sponsoring clinical trial NCT00648661?
This trial is sponsored by Mylan Pharmaceuticals, which has 146 total clinical trials registered on ClinicalTrials.gov.
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