My guest for this interview is Rebecca Matthews, Chief Clinical Operations Officer at Multidisciplinary Association for Psychedelic Studies (MAPS) Public Benefit Corporation.
In this interview, Rebecca shares with us what it takes to conduct clinical trials investigating the use of MDMA, a psychedelic drug, in conjunction with psychotherapy to treat patients with post traumatic stress disorder (PTSD).
PTSD can occur after a person experiences a significant trauma, like a sexual assault, severe physical assault, significant threat to life arising from a hate crime, natural disaster, war, or accident. It affects people of all races, ages, and backgrounds.
As you’ll hear from Rebecca shortly, the clinical data from the recent clinical trial looks extremely promising.
This interview will leave you with excellent insights on differences and challenges of conducting research with psychedelic drugs including site selection, patient recruitment, clinical trial design considerations and more.
I am beyond excited to discuss this important topic of psychedelic research on the podcast.
Please join me in welcoming Rebecca Matthews on the Clinical Trial Podcast. Enjoy!
Podcast Sponsor
This interview you brought you Florence Healthcare.
Transform your Clinical Trials with the #1 Platform for Electronic Document Workflows and Remote Site Access.
Learn how Florence Healthcare helps over 7,200 research sites, sponsors, and CROs across 27 countries take their day back from paper.
Diabetes Clinical Trials with Dr. Stayce Beck
Access to Novel Medical Products with Dr. Alison Bateman-House
Clinical Research as a Profession with Erika Stevens
Community Engagement in Clinical Trials with Chris Komelasky
Community health system-based research with JoAnne Levy
Postmarket Surveillance Studies with David Rutledge
Human-centered design role in clinical trials with Bruce Hellman and Ben James
Clinical Trial Site Networks with Christian Burns
Heart Failure Clinical Trials with Sonna Patel-Raman
Medical Imaging for Clinical Trial Sites with Kelie Luby
Risk Management for Clinical Investigators with Bijan Elahi
5 Strategies for Investigator and Steering Committee Meetings with Kunal Sampat
Clinical Trial Outsourcing with Anca Copaescu
Complexity in Early Phase Clinical Trials with Dr. Oren Cohen
Patient Recruitment in Phase I Studies with Dr. Graham Wood
Medical Imaging in Clinical Trials with Elizabeth Dalton
Clinical Research Data Transparency with Darshan Kulkarni
Launching an NIH Funded Study with Dr. Manish Shah
Introduction to Coverage Analysis with Kelly Willenberg
Clinical Data Management with Mariam Mirgoli
Create your
podcast in
minutes
It is Free
The Commercial Edge: Unleash the Power of People
The emPOWERed Half Hour
Reaching your Goals
Insights@work
Business Dad
The Wall Street Skinny
The Ken Coleman Show