A Phase 1, Dose-Ranging Study to Assess Safety and Psychoactive Effects of a Vaporized 5-Methoxy-N, N-Dimethyltryptamine Formulation (GH001) in Healthy Volunteers

Johannes Reckweg, Natasha L Mason, Cees van Leeuwen, Stefan W Toennes, Theis H Terwey, Johannes G Ramaekers, Johannes Reckweg, Natasha L Mason, Cees van Leeuwen, Stefan W Toennes, Theis H Terwey, Johannes G Ramaekers

Abstract

5-Methoxy-N,N-Dimethyltryptamine (5-MeO-DMT) is a tryptamine with ultra-rapid onset and short duration of psychedelic effects. Prospective studies for other tryptamines have suggested beneficial effects on mental health outcomes. In preparation for a study in patients with depression, the present study GH001-HV-101 aimed to assess the impact of four different dose levels of a novel vaporized 5-MeO-DMT formulation (GH001) administered via inhalation as single doses of 2 (N = 4), 6 (N = 6), 12 (N = 4) and 18 mg (N = 4), and in an individualized dose escalation regimen (N = 4) on the safety, tolerability, and the dose-related psychoactive effects in healthy volunteers (N = 22). The psychedelic experience was assessed with a novel Peak Experience Scale (PES), the Mystical Experience Questionnaire (MEQ), the Ego Dissolution Inventory (EDI), the Challenging Experience Questionnaire (CEQ), and the 5-Dimensional Altered States of Consciousness Questionnaire (5D-ASC). Further aims were to assess the impact of 5-MeO-DMT on cognitive functioning, mood, and well-being. Higher doses of 5-MeO-DMT produced significant increments in the intensity of the psychedelic experience ratings as compared to the lowest 2 mg dose on all questionnaires, except the CEQ. Prominent effects were observed following single doses of 6, 12, and 18 mg on PES and MEQ ratings, while maximal effects on PES, MEQ, EDI, and 5D-ASC ratings were observed following individualized dose escalation of 5-MeO-DMT. Measures of cognition, mood, and well-being were not affected by 5-MeO-DMT. Vital signs at 1 and 3 h after administration were not affected and adverse events were generally mild and resolved spontaneously. Individualized dose escalation of 5-MeO-DMT may be preferable over single dose administration for clinical applications that aim to maximize the experience to elicit a strong therapeutic response.

Keywords: 5-MeO-DMT; cognition; dose finding; psychedelic agents; psychoactive.

Conflict of interest statement

This study was funded by GH Research, Dublin, Ireland. JR and JGR are scientific consultants to GH Research. TT is an employee and shareholder of the company GH Research. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Copyright © 2021 Reckweg, Mason, van Leeuwen, Toennes, Terwey and Ramaekers.

Figures

FIGURE 1
FIGURE 1
Mean (SE) and individual retrospective ratings of the acute psychedelic experience (PES, EDI, MEQ, CEQ) per dose level.
FIGURE 2
FIGURE 2
Mean (SE) and individual retrospective ratings of the acute psychedelic experience per dose level for 5 key-dimensions on the 5D-ASC and the overall score.
FIGURE 3
FIGURE 3
Mean (SE) and individual CADSS and DASS ratings per dose level.
FIGURE 4
FIGURE 4
Mean (SE) and individual lapses of attention in the PVT, number of correct responses in the DSST, number of correct inhibitions in the PVT, ratings of satisfaction with life, mindfulness (FFMQ) and BPRS in every dose condition.

References

    1. Abrams D. I., Vizoso H. P., Shade S. B., Jay C., Kelly M. E., Benowitz N. L. (2007). Vaporization as a Smokeless Cannabis Delivery System: a Pilot Study. Clin. Pharmacol. Ther. 82, 572–578. 10.1038/sj.clpt.6100200
    1. Baer R. A., Smith G. T., Hopkins J., Krietemeyer J., Toney L. (2006). Using Self-Report Assessment Methods to Explore Facets of Mindfulness. Assessment. 13, 27–45. 10.1177/1073191105283504
    1. Barker S. A. (2018). N, N-Dimethyltryptamine (DMT), an Endogenous Hallucinogen: Past, Present, and Future Research to Determine Its Role and Function. Front. Neurosci. 12, 536. 10.3389/fnins.2018.00536
    1. Barrett F. S., Bradstreet M. P., Leoutsakos J. S., Johnson M. W., Griffiths R. R. (2016). The Challenging Experience Questionnaire: Characterization of Challenging Experiences With Psilocybin Mushrooms. J. Psychopharmacol. 30, 1279–1295. 10.1177/0269881116678781
    1. Barrett F. S., Johnson M. W., Griffiths R. R. (2015). Validation of the Revised Mystical Experience Questionnaire in Experimental Sessions With Psilocybin. J. Psychopharmacol. 29, 1182–1190. 10.1177/0269881115609019
    1. Barsuglia J., Davis A. K., Palmer R., Lancelotta R., Windham-Herman A. M., Peterson K., et al. (2018). Intensity of Mystical Experiences Occasioned by 5-MeO-DMT and Comparison With a Prior Psilocybin Study. Front. Psychol. 9, 2459. 10.3389/fpsyg.2018.02459
    1. Bogenschutz M. P., Forcehimes A. A., Pommy J. A., Wilcox C. E., Barbosa P. C., Strassman R. J. (2015). Psilocybin-Assisted Treatment for Alcohol Dependence: a Proof-Of-Concept Study. J. Psychopharmacol. 29, 289–299. 10.1177/0269881114565144
    1. Bremner J. D., Krystal J. H., Putnam F. W., Southwick S. M., Marmar C., Charney D. S., et al. (1998). Measurement of Dissociative States With the Clinician-Administered Dissociative States Scale (CADSS). J. Trauma Stress. 11, 125–136. 10.1023/A:1024465317902
    1. Carhart-Harris R., Giribaldi B., Watts R., Baker-Jones M., Murphy-Beiner A., Murphy R., et al. (2021). Trial of Psilocybin versus Escitalopram for Depression. N. Engl. J. Med. 384, 1402–1411. 10.1056/NEJMoa2032994
    1. Carhart-Harris R. L., Goodwin G. M. (2017). The Therapeutic Potential of Psychedelic Drugs: Past, Present, and Future. Neuropsychopharmacology. 42, 2105–2113. 10.1038/npp.2017.84
    1. Davis A. K., Barsuglia J. P., Lancelotta R., Grant R. M., Renn E. (2018). The Epidemiology of 5-Methoxy- N, N-Dimethyltryptamine (5-MeO-DMT) Use: Benefits, Consequences, Patterns of Use, Subjective Effects, and Reasons for Consumption. J. Psychopharmacol. 32, 779–792. 10.1177/0269881118769063
    1. Davis A. K., So S., Lancelotta R., Barsuglia J. P., Griffiths R. R. (2019). 5-Methoxy-N,N-Dimethyltryptamine (5-MeO-DMT) Used in a Naturalistic Group Setting Is Associated With Unintended Improvements in Depression and Anxiety. Am. J. Drug Alcohol. Abuse. 45, 161–169. 10.1080/00952990.2018.1545024
    1. Diener E., Emmons R. A., Larsen R. J., Griffin S. (1985). The Satisfaction With Life Scale. J. Pers Assess. 49, 71–75. 10.1207/s15327752jpa4901_13
    1. Garcia-Romeu A., Griffiths R. R., Johnson M. W. (2014). Psilocybin-Occasioned Mystical Experiences in the Treatment of Tobacco Addiction. Curr. Drug Abuse Rev. 7, 157–164. 10.2174/1874473708666150107121331
    1. Gieringer D., St. Laurent J., Goodrich S. (2004). Cannabis Vaporizer Combines Efficient Delivery of THC With Effective Suppression of Pyrolytic Compounds. J. Cannabis Ther. 4, 7–27. 10.1300/j175v04n01_02
    1. Griffiths R. R., Johnson M. W., Carducci M. A., Umbricht A., Richards W. A., Richards B. D., et al. (2016). Psilocybin Produces Substantial and Sustained Decreases in Depression and Anxiety in Patients With Life-Threatening Cancer: A Randomized Double-Blind Trial. J. Psychopharmacol. 30, 1181–1197. 10.1177/0269881116675513
    1. Hazekamp A., Ruhaak R., Zuurman L., Van Gerven J., Verpoorte R. (2006). Evaluation of a Vaporizing Device (Volcano) for the Pulmonary Administration of Tetrahydrocannabinol. J. Pharm. Sci. 95, 1308–1317. 10.1002/jps.20574
    1. Henry J. D., Crawford J. R. (2005). The Short-Form Version of the Depression Anxiety Stress Scales (DASS-21): Construct Validity and Normative Data in a Large Non-Clinical Sample. Br. J. Clin. Psychol. 44, 227–239. 10.1348/014466505X29657
    1. Hoshino T., Shimodaira K. (1936). Über Die Synthese Des Bufotenin-Methyl-Äthers (5-Methoxy-N-Dimethyl-Tryptamin) Und Bufotenins (Synthesen in Der Indol-Gruppe. Xv). Bull. Chem. Soc. Jpn. 11, 221–224. 10.1246/bcsj.11.221
    1. Johnson M. W., Garcia-Romeu A., Cosimano M. P., Griffiths R. R. (2014). Pilot Study of the 5-HT2AR Agonist Psilocybin in the Treatment of Tobacco Addiction. J. Psychopharmacol. 28, 983–992. 10.1177/0269881114548296
    1. Krebs-Thomson K., Ruiz E. M., Masten V., Buell M., Geyer M. A. (2006). The Roles of 5-HT1A and 5-HT2 Receptors in the Effects of 5-MeO-DMT on Locomotor Activity and Prepulse Inhibition in Rats. Psychopharmacology (Berl). 189, 319–329. 10.1007/s00213-006-0566-1
    1. Lim J., Dinges D. F. (2008). Sleep Deprivation and Vigilant Attention. Ann. N. Y Acad. Sci. 1129, 305–322. 10.1196/annals.1417.002
    1. Madsen M. K., Fisher P. M., Burmester D., Dyssegaard A., Stenbæk D. S., Kristiansen S., et al. (2019). Psychedelic Effects of Psilocybin Correlate With Serotonin 2A Receptor Occupancy and Plasma Psilocin Levels. Neuropsychopharmacology. 44, 1328–1334. 10.1038/s41386-019-0324-9
    1. Nour M. M., Evans L., Nutt D., Carhart-Harris R. L. (2016). Ego-Dissolution and Psychedelics: Validation of the Ego-Dissolution Inventory (EDI). Front. Hum. Neurosci. 10, 269. 10.3389/fnhum.2016.00269
    1. Ott J. (1999). Pharmahuasca: Human Pharmacology of Oral DMT Plus Harmine. J. Psychoactive Drugs. 31, 171–177. 10.1080/02791072.1999.10471741
    1. Overall J. E., Gorham D. R. (1962). The Brief Psychiatric Rating Scale. Psychol. Rep. 10, 799–812. 10.2466/pr0.1962.10.3.799
    1. Pachter I. J., Zacharias D. E., Ribeiro O. (1959). Indole Alkaloids of Acer Saccharinum (The Silver Maple), Dictyoloma Incanescens, Piptadenia Colubrina, and Mimosa Hostilis. J. Org. Chem. 24, 1285–1287. 10.1021/jo01091a032
    1. Palhano-Fontes F., Barreto D., Onias H., Andrade K. C., Novaes M. M., Pessoa J. A., et al. (2019). Rapid Antidepressant Effects of the Psychedelic Ayahuasca in Treatment-Resistant Depression: a Randomized Placebo-Controlled Trial. Psychol. Med. 49, 655–663. 10.1017/S0033291718001356
    1. Ramaekers J. G., Kuypers K. P., Wingen M., Heinecke A., Formisano E. (2009). Involvement of Inferior Parietal Lobules in Prospective Memory Impairment During Acute MDMA (Ecstasy) Intoxication: an Event-Related fMRI Study. Neuropsychopharmacology. 34, 1641–1648. 10.1038/npp.2008.219
    1. Ray T. S. (2010). Psychedelics and the Human Receptorome. PLoS One. 5, e9019. 10.1371/journal.pone.0009019
    1. Reiche S., Hermle L., Gutwinski S., Jungaberle H., Gasser P., Majić T. (2018). Serotonergic Hallucinogens in the Treatment of Anxiety and Depression in Patients Suffering From a Life-Threatening Disease: A Systematic Review. Prog. Neuropsychopharmacol. Biol. Psychiatry. 81, 1–10. 10.1016/j.pnpbp.2017.09.012
    1. Romeo B., Hermand M., Pétillion A., Karila L., Benyamina A. (2021). Clinical and Biological Predictors of Psychedelic Response in the Treatment of Psychiatric and Addictive Disorders: A Systematic Review. J. Psychiatr. Res. 137, 273–282. 10.1016/j.jpsychires.2021.03.002
    1. Roseman L., Nutt D. J., Carhart-Harris R. L. (2017). Quality of Acute Psychedelic Experience Predicts Therapeutic Efficacy of Psilocybin for Treatment-Resistant Depression. Front. Pharmacol. 8, 974. 10.3389/fphar.2017.00974
    1. Ross S., Bossis A., Guss J., Agin-Liebes G., Malone T., Cohen B., et al. (2016). Rapid and Sustained Symptom Reduction Following Psilocybin Treatment for Anxiety and Depression in Patients With Life-Threatening Cancer: a Randomized Controlled Trial. J. Psychopharmacol. 30, 1165–1180. 10.1177/0269881116675512
    1. Royer F. L., Janowitch L. (1973). Performance of Process and Reactive Schizophrenics on a Symbol-Digit Substitution Task. Percept Mot. Skills. 37, 63–70. 10.2466/pms.1973.37.1.63
    1. Schlemmer R. F., Narasimhachari N., Thompson V. D., Davis J. M. (1977). The Effect of a Hallucinogen, 5-methoxy N, N-Dimethyltryptamine, on Primate Social Behavior. Commun. Psychopharmacol. 1 (2), 105–118.
    1. Shen H. W., Jiang X. L., Winter J. C., Yu A. M. (2010). Psychedelic 5-Methoxy-N,n-Dimethyltryptamine: Metabolism, Pharmacokinetics, Drug Interactions, and Pharmacological Actions. Curr. Drug Metab. 11, 659–666. 10.2174/138920010794233495
    1. Shulgin A., Shulgin A. (1997). Tryptamines I Have Known and Loved: The Chemistry Continues. Berkeley, CA: Transform Press.
    1. Spencer D. G., Glaser T., Traber J. (1987). Serotonin Receptor Subtype Mediation of the Interoceptive Discriminative Stimuli Induced by 5-Methoxy-N,n-Dimethyltryptamine. Psychopharmacology (Berl). 93, 158–166. 10.1007/BF00179927
    1. Strassman R. J., Qualls C. R., Berg L. M. (1996). Differential Tolerance to Biological and Subjective Effects of Four Closely Spaced Doses of N,N-Dimethyltryptamine in Humans. Biol. Psychiatry. 39, 784–795. 10.1016/0006-3223(95)00200-6
    1. Strassman R. J., Qualls C. R. (1994). Dose-Response Study of N,N-Dimethyltryptamine in Humans. I. Neuroendocrine, Autonomic, and Cardiovascular Effects. Arch. Gen. Psychiatry. 51, 85–97. 10.1001/archpsyc.1994.03950020009001
    1. Studerus E., Gamma A., Vollenweider F. X. (2010). Psychometric Evaluation of the Altered States of Consciousness Rating Scale (OAV). PloS one. 5, e12412. 10.1371/journal.pone.0012412
    1. Uthaug M. V., Lancelotta R., Szabo A., Davis A. K., Riba J., Ramaekers J. G. (2020). Prospective Examination of Synthetic 5-Methoxy-N,n-Dimethyltryptamine Inhalation: Effects on Salivary IL-6, Cortisol Levels, Affect, and Non-judgment. Psychopharmacology (Berl). 237, 773–785. 10.1007/s00213-019-05414-w
    1. Uthaug M. V., Lancelotta R., Van Oorsouw K., Kuypers K. P. C., Mason N., Rak J., et al. (2019). A Single Inhalation of Vapor From Dried Toad Secretion Containing 5-Methoxy-N,n-Dimethyltryptamine (5-MeO-DMT) in a Naturalistic Setting Is Related to Sustained Enhancement of Satisfaction With Life, Mindfulness-Related Capacities, and a Decrement of Psychopathological Symptoms. Psychopharmacology (Berl). 236, 2653–2666. 10.1007/s00213-019-05236-w
    1. Vollenweider F. X., Vollenweider-Scherpenhuyzen M. F., Bäbler A., Vogel H., Hell D. (1998). Psilocybin Induces Schizophrenia-like Psychosis in Humans via a Serotonin-2 Agonist Action. Neuroreport. 9, 3897–3902. 10.1097/00001756-199812010-00024
    1. Weil A. T., Davis W. (1994). Bufo alvarius: a Potent Hallucinogen of Animal Origin. J. Ethnopharmacol. 41, 1–8. 10.1016/0378-8741(94)90051-5
    1. Winter J. C., Filipink R. A., Timineri D., Helsley S. E., Rabin R. A. (2000). The Paradox of 5-Methoxy-N,n-Dimethyltryptamine: an Indoleamine Hallucinogen That Induces Stimulus Control via 5-HT1A Receptors. Pharmacol. Biochem. Behav. 65, 75–82. 10.1016/s0091-3057(99)00178-1

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