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Shire to Present Scientific Data Across a Range of Psychiatric Disorders at American Psychiatric Association Annual Meeting
Date:5/17/2013

tion in Major Depression in People With or Without Baseline Executive Function Impairment"

Presenter: Andrew Cutler , MD

  • Monday, May 20, 2013; 2:00pm - 4:00pm

Poster #NR9-30: "Lisdexamfetamine Dimesylate Augmentation Therapy in Anxious or Nonanxious Major Depressive Disorder"

Presenter: Bryan Dirks , MD

  • Monday, May 20, 2013; 2:00pm - 4:00pm

Poster #NR9-38: "Post Hoc Analysis of Lisdexamfetamine Dimesylate Augmentation Therapy Effects on Sleep-Related Endpoints in Adults With Major Depressive Disorder"

Presenter: Angelo Sambunaris , MD

Guanfacine Extended Release (Health Economics and Outcomes Research)

  • Monday, May 20, 2013; 11:30pm - 1:00pm

Poster #NR8-51: "Period Prevalence of Stimulant Augmentation Among Adolescents With ADHD in a U.S. Managed Care Population During 2009 and 2010"

Presenter: Vanja Sikirica , PharmD, MPH

ADHD Outcomes Research

  • Monday, May 20, 2013; 11:30am - 1:00pm

Poster #NR8-29: "Long-Term Outcomes in Attention-Deficit/Hyperactivity Disorder (ADHD): A Systematic Review of Self Esteem and Social Functioning"

Presenter: Paul Hodgkins , PhD

ABOUT VYVANSE (lisdexamfetamine dimesylate)

Vyvanse, which was introduced in the United States in July 2007 for the treatment of ADHD in children ages 6 to 12 years, approved in April 2008 to treat ADHD in adults, approved in November 2010 to treat ADHD in adolescents ages 13 to 17, approved in January 2012 for maintenance treatment in adults, and approved in April 2013 for maintenance tr
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SOURCE Shire plc
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