24
Participants
Start Date
April 30, 2008
Primary Completion Date
August 31, 2008
Study Completion Date
August 31, 2008
lisdexamfetamine dimesylate
Subjects will receive Vyvanse 30, 50, or 70 mg per day or placebo capsules orally for up to (a maximum of) seven (7) weeks.
Clinical Study Centers, LLC, Little Rock
Collaborators (1)
Shire
INDUSTRY
Clinical Study Centers, LLC
OTHER