Oxandrolone in Healthy Adults: A Relative Bioavailability Study

PHASE1CompletedINTERVENTIONAL
Enrollment

6

Participants

Timeline

Start Date

July 10, 2017

Primary Completion Date

November 30, 2017

Study Completion Date

November 30, 2017

Conditions
Bioavailability
Interventions
DRUG

Oxandrin

"The primary outcome for this study will be measurements of the pharmacokinetics of a single dose of oxandrolone 0.1 mg/kg both in tablet form and in the MCT oil preparation. Blood samples for pharmacokinetics will be drawn at 9 timepoints.~Safety will be assessed by recording adverse events and assessment of hepatic function at baseline and one week following oxandrolone dosing."

Trial Locations (1)

84113

Primary Children's Hospital, Salt Lake City

All Listed Sponsors
lead

University of Utah

OTHER

NCT03218631 - Oxandrolone in Healthy Adults: A Relative Bioavailability Study | Biotech Hunter | Biotech Hunter