Clinical Trials Directory

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

TypeNameDescription
DRUGOxandroloneTablets, 10mg, single-dose
DRUGOxandrintablets, 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.