AUTHOR=Edinoff Amber N. , Akuly Haseeb A. , Wagner John H. , Boudreaux Megan A. , Kaplan Leah A. , Yusuf Shadman , Neuchat Elisa E. , Cornett Elyse M. , Boyer Andrea G. , Kaye Adam M. , Kaye Alan D. TITLE=Viloxazine in the Treatment of Attention Deficit Hyperactivity Disorder JOURNAL=Frontiers in Psychiatry VOLUME=12 YEAR=2021 URL=https://www.frontiersin.org/journals/psychiatry/articles/10.3389/fpsyt.2021.789982 DOI=10.3389/fpsyt.2021.789982 ISSN=1664-0640 ABSTRACT=
Attention deficit hyperactivity disorder (ADHD) is the most common neurodevelopmental disorder in children. Over the past twenty years, research on the disease and its characteristics and treatment options has grown exponentially. The first-line pharmacologic treatment of ADHD is stimulants, which have a response rate of ~70%. With the support of four phase 3 studies involving more than 1,000 pediatric patients 6–17 years old, the FDA has approved the non-stimulant, serotonin-norepinephrine modulating agent (SNMA) viloxazine in an extended-release capsule (viloxazine ER) for treatment of ADHD in children aged 6–17. Viloxazine modulates serotonergic activity as a selective 5-HT22B receptor antagonist and 5-HT2C receptor agonist and moderately inhibits norepinephrine transporter (NET), thus blocking the reuptake of norepinephrine. A phase 2 study by Johnson et al. found that once-daily dosing of viloxazine ER in 200, 300, or 400 mg dosages in children with ADHD for eight weeks resulted in a statistically significant reduction of ADHD-RS-IV total score. A