At the forefront of the field of psychedelic-assisted therapy, InnerMost is conducting a number of industry-sponsored and independently initiated clinical trials. Building on his 15 years of experience in psychedelic-assisted therapy research, Dr. Casey Paleos guides our research team as Principal Investigator in all current and future trials.
Research into CYB003, a next-generation psilocybin analog, is showing meaningful improvements for some individuals living with depression. This study offers an opportunity to explore how such treatment might support healing for those living with depression.
This is a long-term extension study that allows for open-label dosing or re-dosing—for participants who did not respond in the first two studies, or relapsed during the extension study. Participants will need to complete either of the first two CYB003 for MDD trials to participate.
Frontline healthcare workers endured extraordinary stress during the pandemic, and many continue to carry symptoms of trauma. This study seeks to explore whether MDMA-assisted therapy can provide meaningful relief and support for those who served in these critical roles.
Explore our services in psychedelic-assisted therapy, clinical research, and therapist training—designed to support your healing journey.
Explore common questions about participation in one of our research trials.
If you would like to apply to participate in a research trial at InnerMost, please email our Study Coordinator at liana@innermost.one.
At InnerMost, our clinical trials are designed to carefully explore how psychedelic medicines can be used safely and effectively to support healing. We strive to create a compassionate, supportive environment for participants, while also contributing valuable insights to the growing field of psychedelic research.
Some sponsor trials will compensate you for your participation, which might cover travel and lodging, while others are voluntary. For trials without a budget, participating is of no cost to you beyond travel and lodging.
It depends—some research trials may require that you taper off your medications under the guidance of a physician. In other trials, you may be able to continue your prescribed treatment throughout the study.
Every session takes place in a safe, supportive environment with trained professionals present. You’ll also have preparatory sessions before dosing and integration sessions afterward to help process and apply your experiences.
Not necessarily. Some studies are randomized and double-blind, which means participants may receive either a psychedelic compound or placebo.
If at any point you decide a trial isn’t right for you, you’re welcome to stop. Your well-being is our priority, and we’ll be here to help navigate the withdrawal process if needed.
To stay updated on upcoming trials at InnerMost, check our website periodically and sign up for our newsletter. You can also find other active studies at www.clinicaltrials.gov