Study of Psilocybin Enhanced Group Psychotherapy in Patients With Cancer (HOPE)

• ClinicalTrials.gov Identifier: NCT04522804
• Recruitment Status: Active, not recruiting
• First Posted: August 21, 2020
• Last Update Posted: March 17, 2023
• Sponsor: University of Utah
• Collaborator: Usona Institute
• Information provided by (Responsible Party): University of Utah

Tracking Information

• First Submitted Date: August 18, 2020
• First Posted Date: August 21, 2020
• Last Update Posted Date: March 17, 2023
• Actual Study Start Date: October 4, 2021
• Actual Primary Completion Date: June 11, 2022 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures (submitted: August 19, 2020)

• Number of adverse events (AEs) and serious adverse events (SAEs) characterized by severity [ Time Frame: 8 months ]
  assess the safety of psilocybin in patients with a cancer diagnosis or hematologic malignancy.
• Number of adverse events (AEs) and serious adverse events (SAEs) characterized by duration [ Time Frame: 8 months ]
  assess the safety of psilocybin in patients with a cancer diagnosis or hematologic malignancy.
• Number of adverse events (AEs) and serious adverse events (SAEs) characterized by relationship to study treatment. [ Time Frame: 8 months ]
  assess the safety of psilocybin in patients with a cancer diagnosis or hematologic malignancy.
• Number of adverse events (AEs) and serious adverse events (SAEs) characterized by seriousness [ Time Frame: 8 months ]
  assess the safety of psilocybin in patients with a cancer diagnosis or hematologic malignancy.
• Number of adverse events (AEs) and serious adverse events (SAEs) characterized by type [ Time Frame: 8 months ]
  assess the safety of psilocybin in patients with a cancer diagnosis or hematologic malignancy.
• recruitment of patients with cancer diagnosis or hematologic malignancy [ Time Frame: 18 months ]
  assess the feasibility to recruit patients with a cancer diagnosis or hematologic malignancy
• Enrollment of patients with a cancer diagnosis or hematologic malignancy [ Time Frame: 18 months ]
  assess the feasibility to enroll patients with a cancer diagnosis or hematologic malignancy
• Consent of patients with a cancer diagnosis or hematologic malignancy [ Time Frame: 18 months ]
  assess the feasibility to consent patients with a cancer diagnosis or hematologic malignancy
• Number of adverse events (AEs) and serious adverse events (SAEs) characterized by severity [ Time Frame: 8 months ]
  assess the tolerability of psilocybin in patients with a cancer diagnosis or
• Number of adverse events (AEs) and serious adverse events (SAEs) characterized by relationship to study treatment. [ Time Frame: 8 months ]
  assess the tolerability of psilocybin in patients with a cancer diagnosis or
• Number of adverse events (AEs) and serious adverse events (SAEs) characterized by duration. [ Time Frame: 8 months ]
  assess the tolerability of psilocybin in patients with a cancer diagnosis or
• Number of adverse events (AEs) and serious adverse events (SAEs) characterized by seriousness. [ Time Frame: 8 months ]
  assess the tolerability of psilocybin in patients with a cancer diagnosis or
• Number of adverse events (AEs) and serious adverse events (SAEs) characterized by type. [ Time Frame: 8 months ]
  assess the tolerability of psilocybin in patients with a cancer diagnosis or

• Original Primary Outcome Measures: Same as current
• Current Secondary Outcome Measures: Not Provided
• Original Secondary Outcome Measures: Not Provided
• Current Other Pre-specified Outcome Measures: Not Provided
• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: Study of Psilocybin Enhanced Group Psychotherapy in Patients With Cancer
• Official Title: A Pilot Study of Psilocybin Enhanced Group Psychotherapy in Patients With Cancer

Brief Summary

This pilot project is an open-label trial that will offer psilocybin in a group format to assess the feasibility of offering psilocybin therapy in a group setting with a decreased therapist to subject ratio. Study intervention will involve a group of six patients with one therapist per subject for a 1:1 ratio, thus significantly reducing the total number of therapist hours per subject compared to standard individual therapy protocols.

Two groups of six will be treated on this trial. After the enrollment and treatment of the first group of six patients, accrual will be placed on hold to ensure subject safety. If stopping rules are not met (Section 11), the next group of six patients will be enrolled and treated on study.

The study intervention will include a total of seven group therapy sessions including three 2-hour preparatory sessions, one 8-hour psilocybin session, and one two-hour integration session. The group therapy sessions will occur on a weekly basis, followed one week later by the psilocybin session. The first integration group session will occur 1-2 days following the psilocybin session.

• Detailed Description: Not Provided
• Study Type: Interventional
• Study Phase: Early Phase 1
• Study Design: Allocation: N/A; Intervention Model: Single Group Assignment; Masking: None (Open Label); Primary Purpose: Treatment
• Condition: Cancer

Intervention

Drug: Psilocybin

Psilocybin is a classic psychedelic of medium duration that is well-tolerated and has a documented safety and efficacy record that makes it uniquely well-suited to the existential issues that arise in this patient population. Psilocybin has been described as an 'existential medicine' given patient testimonials as to its acute and lasting effects on interpersonal connection, ability to more deeply engage with meaningful activities and relationships, dramatic reductions in fear of death, and a renewed sense of well-being.

Study Arms

Experimental: Treatment: all patients

Subjects will participate in a total of seven group sessions. There will be 4 or 6 subjects per group and one therapist will be assigned to each subject for a total of 4 or 6 therapists. In addition, there will be one Group Leader that will facilitate the group sessions. Group sessions will occur once per week for approximately five weeks. The first three sessions are "Preparatory" sessions followed by three "Integration" sessions. During the week following the third Preparatory session and prior to the first Integration session, participants will participate in a psilocybin session.

Intervention: Drug: Psilocybin

• Publications *: Not Provided

Recruitment Information

• Recruitment Status: Active, not recruiting
• Actual Enrollment (submitted: August 19, 2020): 12
• Original Estimated Enrollment: Same as current
• Estimated Study Completion Date: February 2024
• Actual Primary Completion Date: June 11, 2022 (Final data collection date for primary outcome measure)

Eligibility Criteria

Inclusion Criteria:

• Male or female subject aged ≥ 25 years old.
• Current diagnosis of cancer and undergoing treatment for their cancer or completed treatment within ≤ 26 weeks of study registration.
• Life expectancy ≥ 3 months.
• Current DSM-V diagnosis of a depression disorder including adjustment disorder with disturbance of mood.
• Not taking regularly scheduled medications to treat depression and/or anxiety, including benzodiazepines, for at least 4 weeks prior to initiation of the study.
• Fluent in English.
• Have a high school or equivalent (e.g., GED) level of education. Volunteers without a high school or equivalent education must demonstrate reading literacy and comprehension sufficient for understanding the consent form and study questionnaires, as evaluated by study staff obtaining consent.
• Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines.
• ECOG Performance Status ≤ 2.
• Have a support person that would be able to escort the subject home on the evening of the psilocybin dosing session.

• Adequate liver function as defined as:

  • Total Bilirubin ≤ 1.5x institutional upper limit of normal (ULN) unless elevated bilirubin is related to Gilbert's Syndrome.
  • AST(SGOT)/ALT(SGPT) ≤ 3 × institutional ULN

• For female subjects: Negative pregnancy test and agreement to use highly effective contraception (as described in Section 7.2) or evidence of post-menopausal status. The post-menopausal status will be defined as having been amenorrheic for 12 months without an alternative medical cause. The following age-specific requirements apply:

  • Women < 50 years of age:

    • Amenorrheic for ≥ 12 months following cessation of exogenous hormonal treatments; and
    • Luteinizing hormone and follicle-stimulating hormone levels in the post-menopausal range for the institution; or
    • Underwent surgical sterilization (bilateral oophorectomy or hysterectomy).

  • Women ≥ 50 years of age:

    • Amenorrheic for 12 months or more following cessation of all exogenous hormonal treatments; or
    • Had radiation-induced menopause with last menses >1 year ago; or
    • Had chemotherapy-induced menopause with last menses >1 year ago; or underwent surgical sterilization (bilateral oophorectomy, bilateral salpingectomy or hysterectomy).
• Agree to refrain from using any psychoactive drugs, including alcoholic beverages, ondansetron, cannabis, and non-routine PRN medications within 24 hours of each psilocybin administration. Exceptions include daily use of caffeine, nicotine, and opioid pain medication (see Section 6.2.2).
• Agree that for one week preceding the psilocybin session, he/she 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 not to use nicotine for at least 2 hours before the psilocybin administration.
• 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 morning of the psilocybin session. If the subject does not routinely consume caffeinated beverages, he or she must agree not to do so on the day of psilocybin administration.
• Subjects requiring opioid use for pain are on a stable pain management regimen. Long-acting opioid medications (e.g., oxycodone sustained-release, morphine sustained release) will be allowed if the last dose occurred at least 6 hours before psilocybin administration; such medication will not be taken again until at least 6 hours after psilocybin administration.

Exclusion Criteria:

• Positive screening SARS-CoV2 (COVID-19) test, symptoms of COVID-19, or contact with someone who has tested positive for COVID-19.
• Prior systemic antidepressants, anti-psychotic, or anxiolytic medication within four weeks prior to study initiation.
• Personal history or immediate family members with schizophrenia, bipolar affective disorder, delusional disorder, schizoaffective disorder, psychosis, or other psychotic spectrum illness.
• Currently meeting DSM-V criteria for Dissociative Disorder, or other psychiatric conditions judged to be incompatible with the establishment of rapport or safe exposure to psilocybin.
• Currently meeting DSM-V criteria for Cluster B Personality Disorder.
• Current or history within the last two years of meeting DSM-V criteria of substance use disorder (excluding caffeine and nicotine).
• Severe depression requiring immediate standard-of-care treatment e,g.,hospitalization.
• Suicidal ideation with active intent or plan to act on suicidal thoughts as assessed by the treating investigator.
• Cancer with known CNS involvement, or other major CNS disease.
• Involvement in another investigational product for the treatment of cancer.
• Known paraneoplastic syndrome or other ectopic hormone production by a tumor.

• The subject has uncontrolled, significant intercurrent or recent illness including, but not limited to, the following conditions:

  • Cardiovascular disorders:

    • Congestive heart failure New York Heart Association Class III or IV
    • Unstable angina pectoris, cardiac hypertrophy, cardiac ischemia, myocardial infarction
    • Uncontrolled hypertension at time of enrollment (BP>140 systolic or 90 diastolic), coronary artery disease, artificial heart valve
    • Prolonged or congenital long QT syndrome (≥480 ms), serious cardiac arrhythmias, tachycardia, a clinically significant screening ECG abnormality

  • Renal insufficiency as defined as creatinine clearance < 40 mL/min calculated by Cockcroft-Gault formula:

    • Males: ((140-age)×weight[kg])/(serum creatinine [mg/dL]×72)
    • Females: (((140-age)×weight[kg])/(serum creatinine [mg/dL]×72))×0.85

  • Hepatic disorders:

    • Active infection including hepatitis B (known positive HBV surface antigen (HBsAg) result) or hepatitis C.
    • Note: Patients with a past or resolved HBV infection (defined as the presence of hepatitis B core antibody [anti-HBc] and absence of HBsAg) are eligible. Patients positive for hepatitis C (HCV) antibody are eligible only if polymerase chain reaction is negative for HCV RNA.
  • Any other condition that would, in the Investigator's judgment, contraindicate the subject's participation in the clinical study due to safety concerns or compliance with clinical study procedures (e.g., infection/inflammation, intestinal obstruction, unable to swallow medication, [patients may not receive the drug through a feeding tube], social/ psychological issues, etc.)
• Known prior severe hypersensitivity to investigational product or any component in its formulations (NCI CTCAE v5.0 Grade ≥ 3).
• Subjects taking prohibited medications as described in Section 6.3.2. A washout period of prohibited medications for a period of at least five half-lives should occur prior to study registration.

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 25 Years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Contacts: Contact information is only displayed when the study is recruiting subjects
• Listed Location Countries: United States

Administrative Information

• NCT Number: NCT04522804
• Other Study ID Numbers: HCI131965
• Has Data Monitoring Committee: Yes

U.S. FDA-regulated Product

• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No

IPD Sharing Statement

• Plan to Share IPD: No

• Current Responsible Party: University of Utah
• Original Responsible Party: Same as current
• Current Study Sponsor: University of Utah
• Original Study Sponsor: Same as current
• Collaborators: Usona Institute

Investigators

• Principal Investigator: Anna Beck, MD; Huntsman Cancer Institute

• PRS Account: University of Utah
• Verification Date: March 2023