Save the date: the FDA will hold an advisory committee meeting to review Lykos Therapeutics’ New Drug Application (NDA) for MDMA-assisted psychotherapy in the treatment of PTSD on June 4th, 2024. The purpose of FDA advisory committees is to provide “independent, expert advice” to the agency [1]. In this case, it will be the agency’s Psychopharmacologic Drugs Advisory Committee (PDAC) that is…

Source

Previous articleMusic for Psychedelic Exploration and the First ‘Choose Your Own Adventure’ Album
Next articleEarly Research, Psychedelics in Palliative Care, and the Intersection of Science and the Sacred