Trials
Search / Trial NCT05651126

Psilocybin in Adults With and Without Autism Spectrum Disorder

Launched by KING'S COLLEGE LONDON · Dec 6, 2022

Trial Information

Current as of February 05, 2025

Recruiting

Keywords

Autism Spectrum Disorder Psilocybin Serotonin Pharmacological Imaging Mri Eeg Psychedelics

ClinConnect Summary

This clinical trial is investigating how a substance called psilocybin affects the brain in adults, specifically comparing those with Autism Spectrum Disorder (ASD) to those without. The researchers want to understand how serotonin, a chemical in the brain that helps regulate mood and behavior, works differently in these two groups. The study is currently looking for participants aged 18 and older who can speak English and are in good health. People with a diagnosis of ASD will need to have their symptoms assessed by a healthcare professional.

Eligible participants can expect to attend study visits where they will receive psilocybin and undergo various evaluations. It's important to note that individuals with certain medical conditions, a history of drug or alcohol abuse, or major mental illnesses will not be able to participate. Additionally, women must use effective birth control and agree to pregnancy tests before taking the study drug. This trial aims to provide valuable insights into how psilocybin may influence brain function in different populations, which could help improve understanding and treatment of ASD in the future.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • For all participants:
  • Calendar age above 18 years
  • Working knowledge of English
  • Able to give informed consent
  • Not pregnant or breastfeeding
  • Individuals should be in good physical health, prescription medication free during the 2-week period preceding a study visit. However, occasional use of over-the-counter medication (e.g. painkillers) on an as needed basis (and not on the day of study visit) may be permitted. In addition, regular prescription medication (use of a stable dose over the two months preceding participation) with a drug that does not affect 5HT directly may be permitted. Also permitted is topical medication without systemic exposure
  • For individuals with ASD:
  • Diagnosis of ASD by recognised clinical service supported by the Autism Diagnostic Interview-Revised (ADI-R) if a relative is available. Current symptom level assessed using the Autism Diagnostic Observation Schedule (ADOS-2)
  • Exclusion Criteria:
  • For all participants:
  • History of allergy/idiosyncrasy to psilocybin or chemically related compounds or excipients which may be employed in the study or to any other drug used in the past
  • Clinically relevant history or presence of any medical disorder, potentially interfering with this study
  • Clinically relevant abnormality at screening as judged by the investigator
  • History of or current abuse of drugs (including prescription medication) or alcohol or solvents
  • Participation in a research study involving a pharmacological probe or drug trial within last month
  • Subjects with current epilepsy, seizures or episodes of unexplained and unprovoked loss of consciousness
  • Anyone with a history or examination which indicates laboratory testing is needed will be excluded from the study
  • Intelligence Quotient below 70
  • Currently taking prescription medications of propranolol or pindolol
  • Individuals with major mental illness
  • Individuals who have a current or past history of meeting diagnostic criteria for schizophrenia or other psychotic disorders or bipolar I or II disorder
  • Reproductive safety:
  • Pregnancy or breastfeeding (is a routine exclusion for research MRI scanning)
  • Female study participants must be willing to use one form of highly effective non-hormonal contraception for one week after study drug administration. This would include a vasectomised partner (sole partner), tubal occlusion, intrauterine system \[IUS\]/hormonal coil or copper containing intrauterine device or copper containing IUD, or true abstinence (when this is in line with the preferred and usual lifestyle of the subject). Women should have been stable on their chosen method of birth control for a minimum of 2 months before entering the study. Participants must agree to undergo a pregnancy test prior to each administration of study drug
  • For individuals with ASD:
  • ASD caused by a known genetic syndrome, e.g. Fragile X, 22q11 deletion syndrome.
  • Currently treated for epilepsy

About King's College London

King's College London is a prominent research institution renowned for its commitment to advancing healthcare through innovative clinical trials. With a strong emphasis on interdisciplinary collaboration, the college leverages its extensive expertise in medicine, neuroscience, and public health to conduct rigorous studies aimed at improving patient outcomes. As a sponsor of clinical trials, King's College London prioritizes ethical standards, participant safety, and scientific integrity, fostering an environment that encourages groundbreaking research and the translation of findings into clinical practice. Through its state-of-the-art facilities and a diverse network of researchers, the institution strives to address critical health challenges and contribute to the global body of medical knowledge.

Locations

London, , United Kingdom

People applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Discussion 0

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