Study of Psilocybin for Anorexia in Young Adults

Ki vehet részt

• Able to understand and provide informed consent
• Between 18 and 25 years old at time of screening
• Meets Diagnostic and Statistical Manual (DSM-5) criteria for any type of Anorexia Nervosa
• Currently experiencing symptoms of Anorexia Nervosa
• Comfortable reading and writing in English
• Have no anticipated changes in medication or surgical procedures for trial duration
• Commit to attend all in-person and remote study visits and participate in all data collection procedures
• Able to identify one or two family members or close friends to co-enroll in the study, who will be required to participate in select therapy sessions
• Agree to use a highly effective form of contraception for two weeks prior to starting the study and one month after finishing the study
• Agree that for one week preceding each psilocybin session, they will refrain from taking any nonprescription medication, nutritional supplement, or herbal supplement except when approved by the research team. Exceptions will be evaluated by the research team and will include acetaminophen, non-steroidal anti-inflammatory drugs, and common doses of vitamins and minerals
• Agree to consume approximately the same amount of caffeine-containing beverages (e.g., coffee, tea) that they usually consume before arriving at the research unit on the mornings of psilocybin administration sessions. If the young adult participant does not routinely consume caffeinated beverages, they must agree not to do so prior to psilocybin administration sessions

Ki nem vehet részt

• Unwilling to abstain from alcohol, Cannabidiol (CBD), tetrahydrocannabinol (THC), marijuana, and illicit drug use for 48 hours pre and post psilocybin dosing days and abstain from nicotine for 10 hours pre and post psilocybin dosing
• Use of any prohibited concomitant medications or inability or unwillingness to discontinue according to the study's prescribed medication taper or tapering with the participants primary prescriber
• Personal history of bipolar disorder, or psychotic disorder verified by the Structured Clinical Interview for DSM-5 (SCID) and medical history at screening
• Unstable vital signs including Blood Pressure, Heart Rate, or Temperature
• History of cardiovascular disease
• Uncontrolled endocrine conditions, including diabetes, hyper or hypothyroidism
• Significant and uncontrolled gastrointestinal illness at the discretion of the investigator
• Significant and uncontrolled neurological disease including uncontrolled seizure disorder at the discretion of the investigator
• Allergy or intolerance to any of the materials contained in the drug product
• History of severe reaction to psychedelics at the discretion of the investigators
• Mental health condition that will prevent engagement with the treatment team
• Abnormal Safety Labs including sodium, potassium, magnesium, phosphorus, creatinine, estimated Glomerular Filtration Rate, Aspartate Transferase, Alanine Transaminase
• Current known pregnancy or positive pregnancy test at any time during the study
• Body Mass Index less than 12 at screening
• Electrocardiogram abnormalities
• Hospitalization or participation in a residential program for more than 2 of the past 4 weeks at the time of screening
• Positive urine toxicology testing for amphetamines, benzodiazepines, cocaine, cannabis, 3,4-Methylenedioxymethamphetamine (MDMA), and opioids (including methadone and buprenorphine) on the morning of either psilocybin administration session
• Needle phobia
• Simultaneous enrollment in another clinical trial
• Pregnant or Breast feeding
• High risk of self-harm/suicide
• Unwilling or unable to participate in the treatment protocol as planned, including hydration with sports drinks on dosing days
• If any study physician feels that it would be unsafe to continue for any mental, physical or other reason