Clinical Trials Directory

Trials / Completed

CompletedNCT00653393

Bioavailability Study of Tranylcypromine 10mg Tablets Under Fasting Conditions

To Compare Bioavailability of Kali Tranylcypromine 10mg Tablets to That of Parnate 10 mg Tablets Under Fasting Conditions.

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
39 (actual)
Sponsor
Par Pharmaceutical, Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

To compare the single-dose Bioavailability of Tranylcypromine and Parnate

Detailed description

To compare the relative Bioavailability of Tranylcypromine 10 mg tablets with that of PARNATE 10mg tablets in normal,healthy, men and women under fasting conditions

Conditions

Interventions

TypeNameDescription
DRUGTranylcypromineTablets, 10 mg, single-dose
DRUGParnateTablets, 10 mg, single-dose

Timeline

Start date
2004-10-01
Primary completion
2004-11-01
Completion
2004-12-01
First posted
2008-04-04
Last updated
2008-04-04

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00653393. Inclusion in this directory is not an endorsement.