Evaluation of Psilocybin-assisted Psychotherapy (PaP) for the Treatment of Post-traumatic Stress Disorder (PTSD) in Military Veterans

Inclusion Criteria: Aged 18-65 years Fluent in English (reading and speaking) Has internet access via computer or tablet Is able to commit to the study visits and treatment length Can provide a contact (relative, close friend, other support person) who is able to accompany the participant to dosing visits Agrees to inform researchers within 48 hours of any medical treatments or procedures Can swallow pills Agrees to lifestyle restrictions: not to consume alcohol within 24 hours prior to dosing, and to not consume more caffeine than usual Agrees to not participate in any other clinical trials for the duration of the study PCL-5 score ≥33 At least one unsuccessful evidence-based psychotherapy/pharmacotherapy for PTSD Exclusion Criteria: General exclusion criteria: History of poor cooperation or unreliability Engaged in compensation litigation whereby financial game would be achieved from prolonged symptoms of PTSD or any other psychiatric disorders Any other current problems that may interfere with participation (e.g., availability, private space for sessions at home) Has hearing impairment that could interfere with ability to participate in the study Is unable to provide written informed consent Has known hypersensitivity or previous allergic reaction to any constituent of psilocybin Pregnant or breastfeeding BMI <18 or >35 or non-consent for metric to be measured during assessment visit Has been diagnosed with, or has first degree relative with schizophrenia, psychotic disorder (unless substance induced or due to medical condition), or bipolar I disorder Current alcohol or substance use disorder (other than caffeine or nicotine) requiring detox, or currently in withdrawal from such disorder. Exception for milder disorder if realistic plan (agreed by researcher, therapy team, and medical monitor) for successfully mitigating alcohol/substance use to prevent use from impacting participation, safety, and/or efficacy of the treatment. Mental health exclusion: Schizophrenia spectrum or other psychotic disorders or first degree relative with such disorders (incl. major depressive disorder with psychotic features, or Bipolar I or II disorders) May present serious risk to others (established via clinical interview and contact with treating psychiatrist) Is likely to be re-exposed to index trauma or other significant trauma, lack social support, or lack of stable living situation Physical health exclusion: History of myocardial infarction, angina, cerebrovascular accident, aneurysm, or pulmonary vascular disease Has had Transient Ischemic Attack (TIA) within past 6 months Has uncontrolled hypertension (140/90 mmHG or higher assessed on three separate occasions). Adequately controlled hypertension does not exclude participant Has Wolff-Parkinson-White syndrome or other accessory pathway conditions that have not been successfully eliminated by ablation History of arrhythmia, other than premature atrial contractions (PACs) or occasional premature ventricular contractions (PVCs) in the absence of ischemic heart disease, within past 12 month History of risk factors for Torsade de pointes (e.g., heart failure, hypokalemia, Long QT Syndrome family history) Requires use of concomitant medications that may prolong the QT/QTc interval during psilocybin dosing sessions Marked Baseline prolongation of QT/corrected QT interval (QTc; e.g., repeated demonstration of a QTc interval >450ms and >460ms in females corrected by Bazett's formula). For transgender or non-binary subjects, QTc interval will be evaluated based on sex assigned at birth, unless the subject has been on hormonal treatment for five or more years. History of medical condition that could make receiving a sympathomimetic drug harmful because of increased blood pressure and heart rate Haptic enzymes alkaline phosphatase (ALP), alanine transaminase (ALT), Aspartate aminotransferase (AST) or Gamma-glutamyl Transferase (GGT) > three times upper limit of normal (ULN), or total bilirubin levels >2x ULN Previous indication of liver or kidney damage Current Hepatitis C virus (HCV) infection - Asymptomatic HCV permitted if previously undergone evaluation and treatment as needed Current uncontrolled Type 2 diabetes mellitus Current uncontrolled hypothyroidism Current or historic glaucoma unless participation approved by an ophthalmologist History of traumatic brain injury (TBI)/cognitive impairment limiting ability to engage in treatment (e.g., memory or concentration problems, impulsivity related to brain injury) Current neurological illness including, but not limited to, seizure disorders, frequent migraines (or on prophylaxis for same), multiple sclerosis, movement disorders, history of significant head trauma, or central nervous system (CNS) tumour) The presence of other severe acute or chronic medical condition, psychiatric condition or laboratory abnormality that may increase the risk associated with participation or may interfere with interpretation of trial results. Please note: mild, stable chronic medical problems (e.g., Type 1 or 2 Diabetes Mellitus, HIV infection, glaucoma, hypothyroidism, hepatitis C, hepatic or renal disease, etc.) may be enrolled if Investigator and research psychiatrist agree that condition(s) would not: significantly increase risk of psilocybin administration, or be likely to produce significant symptoms during the study that could interfere with participation, or be confused with side effects of Investigational Product Previous use of psilocybin or other psychedelic substance (except cannabis) on more than 5 occasions and/or use of the same within the past 5 years Previous use of psilocybin, methylenedioxymethamphetamine (MDMA), ketamine (or substances reportedly containing psilocybin, MDMA, or ketamine) with therapeutic aim for current PTSD diagnosis Has received Electroconvulsive Therapy (ECT) within 12 weeks of enrolment Requires ongoing concomitant therapy with a psychiatric medication (unless deemed acceptable by the research psychiatrist) Exposure to other investigational drug/device within 30 days of enrolment Medication exclusion criteria: Over-the-counter products intended to affect mood/anxiety Efavirenz Lithium "Rest-Category" Antidepressants (e.g., mirtazapine, trazodone, bupropion); Exception if ≤7.5mg mirtazapine, or ≤50mg trazodone as sleeping medication Antipsychotics/Neuroleptics; Exception if ≤50mg quetiapine as sleeping medication Stimulants The following medications are permitted if the dose is hypnotic: selective serotonin reuptake inhibitor (SSRIs); Tricyclic antidepressants (TCAs); monoamine oxidase inhibitor (MAOIs) The following medications are permitted if their use is unaltered during the study: Benzodiazepines "Z-drugs" (e.g., zolpidem); Anticonvulsants; Antihistamines Medications which are permitted as determined case-by-case by research psychiatrist: non-psychiatric, but mind-altering medication (e.g., morphine, dexamethasone, etc.). Not to be used 72hrs prior to psilocybin dosing session: Sildenafil (Viagra), tadalafil, or similar medications Not to be used on dosing days and research psychiatrist discretion: Medical cannabis Risk exclusion criteria: Current suicidal ideation/intent/action Previous (within previous 6 months) suicidal ideation/intent/action Current and previous deliberate self-harm