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Centanafadine’s Route to FDA Review: A Clinical Path of the ADHD Medication

 ADHD in the News 2026-07-23


Centanafadine, a first-in-class norepinephrine-dopamine-serotonin reuptake inhibitor (NDSRI), awaits a regulatory decision by the US Food and Drug Administration (FDA) on Friday, July 24. Ahead of the FDA action, review the path of Otsuka Pharmaceutical’s centanafadine for treatment of ADHD.

View Article: Psychiatric Times, July 23, 2026




Other Articles in this Edition

Next steps after your child is diagnosed with ADHD

New study links ADHD symptoms in boys and addictive social media use 

At What Age Should Your Neurodivergent Child Get a Cell Phone?

They watched TikToks about ADHD, anxiety and cancer. Then they worried they had them

What is ‘popcorn brain’ and how to help it 

Lurie Children’s Program Helps Pediatricians Gain Independent Expertise to Treat More Kids with Depression and Anxiety, Study Finds

What Is Your Building Communicating to Students?

How telehealth is fuelling a surge in ADHD scripts in a business model that benefits the rich 

New Meta-analysis Finds Structured Executive Function Training Largely Ineffective 

Study Maps Accelerated Brain Aging Signatures Across 9 Conditions

Centanafadine’s Route to FDA Review: A Clinical Path of the ADHD Medication

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