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Trials / Completed

CompletedNCT00648570

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.

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
37 (actual)
Sponsor
Mylan Pharmaceuticals Inc · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGEscitalopram Oxalate Tablets 20 mg20mg, single dose fasting
DRUGLexapro® Tablets (20 mg20mg, single dose fasting

Timeline

Start date
2004-08-01
Primary completion
2004-10-01
Completion
2004-10-01
First posted
2008-04-01
Last updated
2024-04-24

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00648570. Inclusion in this directory is not an endorsement.

Fasting Study of Escitalopram Oxalate Tablets 20 mg and Lexapro® Tablets 20 mg (NCT00648570) · Clinical Trials Directory