2024 - Shifting Perceptions in Psychedelics: Challenges and Progress in Drug Development
Date2024-11-14
Deadline2024-11-14
VenueONLINE-VIRTUAL, USA - United States
KeywordsLife Sciences; Clinical Trials; Drug Discovery & Development
Topics/Call fo Papers
Psychedelic drugs may offer promise for the treatment of certain mental health conditions, such as post-traumatic stress disorder (PTSD), but the development process is less straightforward than traditional medicines due to negative preconceptions and clinical study complexity.
As psychedelics move from recreational use into clinical development, there is a need for greater clarity on the regulatory framework for these therapeutics. Psychedelic studies also present unique challenges related to protocol design, site selection and study execution.
In this webinar, the expert speakers will explore the current landscape of psychedelic clinical development and discuss critical considerations for ensuring scientific rigor, patient safety, data quality and ethical conduct. They will also provide a comprehensive review of the recent advisory committee (ADCOM) meeting and the FDA action letter concerning Lykos’ new drug application (NDA) for the use of 3,4-methylenedioxymethamphetamine (MDMA) as a treatment for PTSD.
The attendees will gain a better understanding of the regulatory landscape for clinical trials involving psychedelic drugs, including current perspectives and guidance that can influence study design and execution. The speakers will explore the key considerations necessary for designing and operationalizing studies within this unique and emerging field.
Register for this webinar to explore the emerging field of psychedelic clinical development and gain insights into the regulatory frameworks and unique challenges associated with these therapies.
Keywords: Clinical Trials, Drug Development, Clinical Research, CRO, Neurodegenerative Disease, PTSD, Regulatory, CNS, Neurology, Psychedelics, Psychedelic Drug, CNS Drug Development
As psychedelics move from recreational use into clinical development, there is a need for greater clarity on the regulatory framework for these therapeutics. Psychedelic studies also present unique challenges related to protocol design, site selection and study execution.
In this webinar, the expert speakers will explore the current landscape of psychedelic clinical development and discuss critical considerations for ensuring scientific rigor, patient safety, data quality and ethical conduct. They will also provide a comprehensive review of the recent advisory committee (ADCOM) meeting and the FDA action letter concerning Lykos’ new drug application (NDA) for the use of 3,4-methylenedioxymethamphetamine (MDMA) as a treatment for PTSD.
The attendees will gain a better understanding of the regulatory landscape for clinical trials involving psychedelic drugs, including current perspectives and guidance that can influence study design and execution. The speakers will explore the key considerations necessary for designing and operationalizing studies within this unique and emerging field.
Register for this webinar to explore the emerging field of psychedelic clinical development and gain insights into the regulatory frameworks and unique challenges associated with these therapies.
Keywords: Clinical Trials, Drug Development, Clinical Research, CRO, Neurodegenerative Disease, PTSD, Regulatory, CNS, Neurology, Psychedelics, Psychedelic Drug, CNS Drug Development
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Last modified: 2024-10-16 04:52:35