The purpose of this study is to measure safety and the improvement in symptoms in subjects with ADHD when taking ALKS 7290 tablets compared with placebo tablets.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
312
Alkermes Investigator Site
Chino, California, United States
RECRUITINGAlkermes Investigator Site
Maitland, Florida, United States
RECRUITINGChange from Baseline to Week 4 in Attention Deficit Disorder Investigator Symptom Rating Scale (AISRS) total score
Time frame: Baseline to Week 4
Change from Baseline to Week 4 in Clinical Global Impression- Severity (CGI-S) scale score
Time frame: Baseline to Week 4
Incidence of treatment-emergent adverse events
Time frame: Up to 6 weeks
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