This week, Antony Loebel, our Chief Medical Officer and President of Clinical Development, and Daniel Bonner, Co-founder, SVP, Platform, presented additional data from our Phase 1 study of SPT-300 at the American College of Neuropsychopharmacology (ACNP) Annual Meeting in Phoenix, Arizona. SPT-300 is an oral prodrug of allopregnanolone that is designed to retain the pharmacological activity of allopregnanolone, an endogenous neurosteroid. Allopregnanolone has been clinically validated in third-party trials as a rapidly acting antidepressant with anxiolytic effects.
New data in the poster include further safety analyses and pharmacokinetic and pharmacodynamic data. Together with previous clinical efficacy data, the further analyses of the Phase 1 study demonstrate that these doses of SPT-300 are well-tolerated and have rapidly acting pharmacodynamic activity. Based on the Phase 1 study results, the profile of SPT-300 is suitable for chronic dosing and oral administration at night in the planned Phase 2b placebo-controlled study in major depressive disorder with or without anxious distress. #ANCP2024
Read more in today’s press release: https://lnkd.in/ec-XK-fS