Overview

Efficacy Study of Lisdexamfetamine to Treat Binge Eating Disorder

Status:
Completed
Trial end date:
2012-10-01
Target enrollment:
0
Participant gender:
All
Summary
The specific aim of this study is to examine the efficacy and safety of lisdexamfetamine compared with placebo in outpatients with binge eating disorder
Phase:
Phase 3
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Lindner Center of HOPE
Collaborators:
Shire
University of Cincinnati
Treatments:
Lisdexamfetamine Dimesylate
Criteria
Inclusion Criteria:

- Patients will meet DSM-IV criteria for BED for at least the last 6 months

Exclusion Criteria:

- Women who are pregnant or lactating and women of childbearing potential who are not
taking adequate contraceptive measures. If there is a possibility a female subject
might be pregnant, a pregnancy test will be performed. (All women of childbearing
potential will have a negative pregnancy test before entering the study.)

- Subjects who are displaying clinically significant suicidality or homicidality.

- A current or recent (within 6 months of the start of study medication) DSM-IV
diagnosis of substance abuse or dependence