Trials / Completed
CompletedNCT00652886
Bioavailability Study of Oxandrolone Tablets Under Fasting Conditions
Compare the Relative Bioavailability of Oxandrolone 10mg Tablets With That of OXANDRIN 10 mg Tablets Following a Single Oral Dose(1*10 mg Tablet) in Healthy, Adult Subjects Under Fasting Conditions.
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 26 (actual)
- Sponsor
- Par Pharmaceutical, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
-To compare the single dose bioavailability of Kali and BTG
Detailed description
-To compare the bioavailability of Oxandrolone 10mg tablets with that of OXANDRIN 10mg tablets following a single -dose in healthy, adult subjects under fasting conditions.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Oxandrolone | Tablets, 10mg, single-dose |
| DRUG | Oxandrin | tablets, 10mg, single-dose |
Timeline
- Start date
- 2005-03-01
- Primary completion
- 2005-03-01
- Completion
- 2005-06-01
- First posted
- 2008-04-04
- Last updated
- 2008-04-04
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00652886. Inclusion in this directory is not an endorsement.