The efficacy, safety, and tolerability of centanafadine SR (200 mg TDD or 400 mg TDD) compared to placebo for the treatment of adults with ADHD
Charlotte, North Carolina
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End Date January 30, 2020
Primary Contact Dr. Anelys Marin, BS, CCRC, RMA, IMG
Email marin@newhcr.com
Phone (980) 209-9784 ext. 2012
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Study Details
Purpose of the Study:
Primary:
To confirm the efficacy of centanafadine sustained-release (SR) tablets administered twice-daily (BID; 200 mg or 400 mg total daily doses [TDDs]) compared to placebo in the treatment of adults with ADHD.
Secondary:
To confirm the safety and tolerability of centanafadine SR tablets administered BID (200 mg or 400 mg TDDs) compared to placebo in the treatment of adults with ADHD.