A novel psychedelic 5-HT <sub>2A</sub> receptor agonist GM-2505: The pharmacokinetic, safety, and pharmacodynamic profile from a randomized trial healthy volunteer

These PD findings were similar in nature and magnitude to other 5-HT<sub>2A</sub> receptor agonists that have been studied clinically. In line with the GM-2505 PK profile, the duration of cardiovascular and subjective effects was shorter than psilocybin but longer than DMT, demonstrating a potentially more practical temporal profile for use in a supervised clinical setting compared to longer-acting 5-HT<sub>2A</sub> receptor agonists, with an optimal dose range of 10-15 mg IV. Clinical trial (ISRCTN64428072) registration: https://www.isrctn.com/ISRCTN64428072.

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Publication Details

Journal
Journal of Psychopharmacology
Published
2025-10-16
DOI
https://doi.org/10.1177/02698811251378512
Citations
1
Primary Topic
Psychedelics and Drug Studies
Type
article
Field-Weighted Citation Impact
2.31
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article

A novel psychedelic 5-HT 2A receptor agonist GM-2505: The pharmacokinetic, safety, and pharmacodynamic profile from a randomized trial healthy volunteer

Gerard J. Marek, Eric W. Austin, Shane Raines, Adam K. Klein et al.
1 citations
Journal of Psychopharmacology
Psychedelics and Drug Studies
2.31
article

A novel psychedelic 5-HT 2A receptor agonist GM-2505: The pharmacokinetic, safety, and pharmacodynamic profile from a randomized trial healthy volunteer

Gerard J. Marek, Eric W. Austin, Shane Raines, Adam K. Klein, Zoë A. Hughes, Wai Yie Leong, Soma Makai‐Bölöni, Daniel Umbricht, Marije E. Otto, Jonathan Sporn, Laura Borghans, Maria Joanna Juachon, Andrew C. Kruegel, Dino Dvořák, Jason Winters, Fas J. Krol, Gabriël E. Jacobs, Edward P. Christian, Anne J. van der Graaf
article en
1 citations

Abstract

These PD findings were similar in nature and magnitude to other 5-HT<sub>2A</sub> receptor agonists that have been studied clinically. In line with the GM-2505 PK profile, the duration of cardiovascular and subjective effects was shorter than psilocybin but longer than DMT, demonstrating a potentially more practical temporal profile for use in a supervised clinical setting compared to longer-acting 5-HT<sub>2A</sub> receptor agonists, with an optimal dose range of 10-15 mg IV. Clinical trial (ISRCTN64428072) registration: https://www.isrctn.com/ISRCTN64428072.

Journal of Psychopharmacology
Leiden University (NL), Leiden University Medical Center (NL), Centre for Human Drug Research (NL)
Openalex Percentile: Top 10%
Psychedelics and Drug Studies
2.31
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