Treatment of Impulsive Aggression in Subjects With ADHD in Conjunction With Standard ADHD Treatment (CHIME 2)



Status:Recruiting
Conditions:Psychiatric, ADHD
Therapuetic Areas:Psychiatry / Psychology, Other
Healthy:No
Age Range:6 - 12
Updated:3/11/2017
Start Date:March 2015
Contact:Stefan Schwabe, MD, PhD
Email:sschwabe@supernus.com
Phone:301-838-2527

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The purpose of this study is to demonstrate the efficacy, safety and tolerability of SPN-810
in the treatment of impulsive aggression in patients with Attention Deficit/Hyperactivity
Disorder (ADHD) in conjunction with standard ADHD treatment. Approximately 291 subjects aged
6 to 12 years with ADHD and comorbid impulsive aggression will be recruited in this study.
The frequency of impulsive aggression behaviors will be assessed as a primary outcome.
Additionally, the severity and improvement in impulsive aggression, and quality of life
measures for the subject and caregiver will be assessed using validated scales.


Inclusion Criteria:

- Otherwise healthy male or female subjects, age 6 to 12 years at the time of screening
with a primary diagnosis of ADHD and currently receiving monotherapy treatment with
an optimized FDA-approved ADHD medication.

- Impulsive aggression will be confirmed at screening using R-MOAS and Vitiello
Aggression Scale.

Exclusion Criteria:

- Current or lifetime diagnosis of epilepsy, major depressive disorder, bipolar
disorder, schizophrenia or related disorder, personality disorder, Tourette's
disorder, or psychosis not otherwise specified.

- Currently meeting DSM criteria for autism spectrum disorder, pervasive developmental
disorder, obsessive compulsive disorder, post-traumatic stress disorder, or any other
anxiety disorder as primary diagnosis.

- Known or suspected intelligence quotient (IQ) < 70, suicidality, pregnancy, or
substance or alcohol abuse.
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