Cingulate Outlines Plan For Pivotal Attention Deficit/Hyperactivity Disorder Studies

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Cingulate Inc CING plans to initiate Phase 3 studies for CTx-1301 for Attention Deficit/Hyperactivity Disorder (ADHD) in 2022.

  • ADHD is a chronic neurobiological and developmental disorder.
  • The planned studies include a fixed-dose pediatric & adolescent safety and efficacy study, a dose-optimization study extension, and a pediatric safety & efficacy study to assess the onset and duration of efficacy. 
  • Specifically, the pivotal, fixed-dose study will begin in Q2 of 2022. 
  • These studies are instrumental for the filing of the New Drug Application to the FDA, expected in 2H of 2023.
  • Based on feedback from the FDA regarding the CTx-1301 initial Pediatric Study Plan and longstanding guidance on the 505(b)(2) pathway, Cingulate has accelerated its study timeline, with a strong likelihood of reducing capital requirements by condensing the number and design of studies, therefore potentially reducing its time to approval.
  • Price Action: CING shares are down 5.46% at $1.73 during the market session on the last check Tuesday.
Posted In: BiotechNewsPenny StocksHealth CareMoversTrading IdeasGeneralBriefsPhase 3 Trial

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