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Axsome Therapeutics Reports the First Patient Dosing of Solriamfetol in the P-III Trial (FOCUS) for Adults with Attention Deficit Hyperactivity Disorder

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Axsome Therapeutics Reports the First Patient Dosing of Solriamfetol in the P-III Trial (FOCUS) for Adults with Attention Deficit Hyperactivity Disorder

Shots:

  • The first patient has been dosed in the P-III trial (FOCUS) evaluating the efficacy and safety of solriamfetol (150 or 300mg) vs PBO in a ratio (1:1:1) in ~ 450 patients with ADHD for 6wks.
  • The 1EPs of the study will be changed in the adult ADHD investigator symptom report scale (AISRS)
  • Solriamfetol, a dopamine and norepinephrine reuptake inhibitor. Additionally, Solriamfetol has agonist action at the 5HT1a and trace amine-associated receptor 1 (TAAR1) receptors, according to in vitro studies

Ref: GlobeNewswire | Image: Axsome Therapeutics

Related Post:- Axsome Therapeutics Entered into an Exclusive License Agreement with Pharmanovia to Develop and Commercialize Sunosi (solriamfetol) in Europe

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Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

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