Effects of Exenatide on Overweight Adolescents With Prader-Willi Syndrome

NACompletedINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

March 31, 2012

Primary Completion Date

May 31, 2013

Study Completion Date

December 31, 2013

Conditions
Prader-Willi Syndrome
Interventions
DRUG

Exenatide

The investigators will give patients naive to GLP-1 agonists exenatide per manufacturer dosing recommendations for 6 months. The investigators will begin by giving 5 mcg subcutaneously twice a day for 1 month and then increase the dose to 10 mcg subcutaneously twice a day for the remainder of the study (5 months).

Trial Locations (1)

90027

Children's Hospital of Los Angeles, Los Angeles

All Listed Sponsors
lead

Children's Hospital Los Angeles

OTHER

NCT01444898 - Effects of Exenatide on Overweight Adolescents With Prader-Willi Syndrome | Biotech Hunter | Biotech Hunter