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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.