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
| Type | Name | Description |
|---|---|---|
| DRUG | Tranylcypromine | Tablets, 10 mg, single-dose |
| DRUG | Parnate | Tablets, 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.