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The primary objective of this study is to assess the time of onset and time course of efficacy over 16 hours of PRC-063 compared to placebo in adults diagnosed with ADHD in a simulated adult workplace...
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Lead Sponsor
Rhodes Pharmaceuticals, L.P.
Collaborators
NCT06810180 · Attention Deficit Hyperactivity Disorder (ADHD), Sleep, and more
NCT07189442 · Attention Deficit Hyperactivity Disorder (ADHD), Autism Spectrum Disorder (ASD)
NCT07180758 · Attention Deficit Hyperactivity Disorder (ADHD)
NCT07459699 · Attention Deficit Hyperactivity Disorder (ADHD)
NCT04943796 · Attention Deficit Hyperactivity Disorder (ADHD)
AVIDA, Inc.
Newport Beach, California
Center for Psychiatry and Behavioral Medicine Inc.
Las Vegas, Nevada
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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