Exploring the effects of psychoactive substances similar to classic psychedelics
Investigation of Psychedelic Effects in Psychoactive Substances
This study is testing whether new psychoactive substances can create experiences like classic psychedelics in healthy volunteers.
Quick facts
| Phase | Phase 1 |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 25 Years to 55 Years |
| Sex | All |
| Sponsor | Johns Hopkins University Academic / other |
| Locations | 1 site (Baltimore, Maryland) |
| Trial ID | NCT06772753 on ClinicalTrials.gov |
What this trial studies
This double-blind, placebo-controlled study investigates whether various psychoactive substances can induce experiences similar to those produced by classic psychedelics in healthy volunteers. Participants will undergo a thorough screening process and may participate in up to six experimental drug administration sessions, where they will receive either a psychoactive substance or a placebo. The study employs a randomized design to ensure that neither participants nor staff know which substance is being administered on any given day. Additionally, participants will engage in preparation sessions and follow-up visits to discuss their subjective experiences.
Who should consider this trial
Good fit: Ideal candidates are healthy adults aged 25 to 55 with a BMI between 18 and 34.
Not a fit: Patients with a history of significant medical or psychological issues may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance our understanding of the therapeutic potential of psychoactive substances for mental health treatment.
How similar studies have performed: Other studies have shown promising results in exploring the effects of psychedelics, suggesting potential for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Be 25 to 55 years old * BMI between 18 and 34 kg/m2 * Agree to consume approximately the same amount of caffeine-containing beverage (e.g., coffee, tea) that he/she consumes on a usual morning, before arriving at the research unit on the mornings of drug session days. If the subject does not usually consume caffeinated beverages, he or she must agree not to do so on session days * Agree to refrain from using any psychoactive drugs, including alcoholic beverages, within 24 hours of each drug administration. Exceptions include daily use of caffeine and nicotine. * Be healthy and psychologically stable as determined by screening for medical problems via a personal interview, a medical questionnaire, a physical examination, an electrocardiogram (ECG), and routine medical blood and urinalysis laboratory tests * Agree not to take any PRN prescription medications on the mornings of the sessions unless deemed appropriate by study team. Exclusion Criteria: * Women who are pregnant (as indicated by a positive urine pregnancy test assessed at intake and before each drug session) or nursing; women who are of child-bearing potential and sexually active who are not practicing an effective means of birth control (e.g. oral contraceptives, intrauterine device) * Cardiovascular conditions-coronary artery disease, stroke, angina, uncontrolled hypertension, a clinically significant ECG abnormality (e.g., atrial fibrillation), or transient ischemic attack-that in the clinical opinion of the screening physician or mid-level provider would put the participant at an especially high risk for adverse effects from the study. * Epilepsy with history of seizures * Insulin-dependent diabetes; if taking oral hypoglycemic agent, then no history of hypoglycemia * Currently taking on a regular (e.g., daily) basis any medications having a primary centrally acting pharmacological effect on serotonin neurons or medications that are Monoamine oxidase (MAO) inhibitors. For individuals who have intermittent or as needed (PRN) use of such medications, sessions will not be conducted until at least 5 half-lives of the agent have elapsed after the last dose. * Use of nonprescription medications, nutritional supplements, or herbal supplements except when approved by the study investigators. Exceptions will be evaluated by the study investigators and will include acetaminophen, non-steroidal anti-inflammatory drugs, and common doses of vitamins and minerals * History of meeting Diagnostic and Statistical Manual of Mental Disorders (DSM)-5 criteria for moderate or severe substance use disorder (including alcohol use disorder, but excluding tobacco), requiring that at least one of the endorsed criteria relates to prior loss of control of substance use (e.g. consuming the substance in larger amounts and for a longer amount of time than intended; persistent desire to cut down or regulate use; unsuccessful attempts to stop use; spending a great deal of time obtaining, using, or recovering from the effects of substance use). * Active suicidal ideation and/or behavior at time of screening. * Psychiatric disorder that in the clinical opinion of the study team would put the participant at an especially high risk for adverse effects from the study. * First-degree relative who meets DSM-5 criteria for a Schizophrenia Spectrum or Other Psychotic Disorder (unless disorder is Substance/Medication-Induced Psychotic Disorder or Psychotic Disorder Due to Another Medical Condition), Bipolar I Disorder, or Bipolar II disorder. * Enrolled in another clinical trial or have received any drug as part of a research study within 30 days prior to dosing. * Known allergy or prior adverse reaction to any of the study drugs judged by the investigator and/or medical staff to put the study volunteer at greater risk. * Known allergy or intolerance to nitroglycerin. * Concomitant use of any CYP2C9 and CYP3A4 inhibitors.
Where this trial is running
Baltimore, Maryland
- Johns Hopkins Center for Psychedelic and Consciousness Research — Baltimore, Maryland, United States (Recruiting)
Study contacts
- Principal investigator: Frederick Barrett, Ph.D. — Johns Hopkins University
- Study coordinator: Zach Daily
- Email: zdaily1@jh.edu
- Phone: 410-550-9777
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.