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Unknown statusPhase 2

The Safety and Efficacy of Psilocybin in Cancer Patients With Major Depressive Disorder

NCT04593563 · Maryland Oncology Hematology, PA

Closed to entry
Status
Not accepting participants
Phase 2
Phase
30
Target enrolment
1
Study sites
1 US states

What it is testing

Summary

This is a Phase II, single-center, fixed dose, open label trial to explore the safety, tolerability and efficacy of a 25mg dose of psilocybin in cancer patients with MDD. The study population will include adult men and women, 18 years of age or above, with MDD, diagnosed with a malignant neoplasm. MDD is defined as those who meet DSM 5 diagnostic criteria for a single or recurrent episode of MDD without psychotic features. A diagnosis of a malignant neoplasm is defined as having a diagnostic code from C00 to C97 according to the ICD-10.

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • The Montgomery-Åsberg Depression Rating Scale (MADRS)

    Measured over 8 weeks

  • Quick Inventory of Depressive Symptomatology Self reported (QIDS-SR)

    Measured over 8 weeks

  • Maudsley Visual Analogue Scale (VAS) current

    Measured over 8 weeks

  • Maudley Visual Analogue Scale (VAS) Change.

    Measured over 8 weeks

  • Pain Visual Analogue Score (VAS)

    Measured over 8 weeks

  • Hamilton Anxiety Rating Scale-A (HAM-A)

    Measured over 8 weeks

  • State-Trait Anxiety Inventory (STAI)

    Measured over 8 weeks

  • National Institute of Health Healing Experience of All Life Stressors (NIH-HEALS)

    Measured over 8 weeks

  • Patient EQ-5D-5L

    Measured over 8 weeks

  • Caregiver Oncology Quality of Life Questionnaire (CarGOQol)

    Measured over 8 weeks

  • DS-II

    Measured over 8 weeks

  • 5 Dimension Altered State of Consciousness (5D-ASC)

    Measured over 8 weeks

  • Sheehan Disability Score (SDS)

    Measured over 8 weeks

  • Scale To Assess Therapeutic Relationship: Patient (STAR-P)

    Measured over 8 weeks

  • Scale To Assess Therapeutic Relationship: Clinician. (STAR-C)

    Measured over 8 weeks

  • Changes in electrocardiographs.

    Measured over 8 weeks

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

18 Years
Ages
All
Sex
Not accepted
Healthy volunteers
Inclusion Criteria: 1. Signed ICF 2. 18 years of age or above at Screening (V1) 3. Currently meet criteria for MDD (single or recurrent episode as defined by DSM 5; if single episode, duration of more or equal to 3 months) based on medical records, clinical assessment and documented completion of the MINI version 7.0.2 4. A diagnosis of a malignant neoplasm with a diagnostic code from C00 to C97 according to the International Classification of Diseases and Related Health Problems, 10th Revision (ICD-10) 5. HAM D 17 score ≥18 at Screening (V1) and at Baseline (V2) 6. Are not currently taking any antidepressant and/or antipsychotic medications, or medical cannabis, at Screening (V1) 7. Able to complete all protocol required assessment tools without any assistance or alteration to the copyrighted assessments, and to comply with all study visits 8. Has capacity to consent (assessed via investigator judgement) Exclusion Criteria: Psychiatric Exclusion Criteria: 1. Current or past history of schizophrenia, psychotic disorder, bipolar disorder, delusional disorder, paranoid personality disorder, schizoaffective disorder, or borderline personality disorder, as assessed by medical history and a structured clinical interview (MINI version 7.0.2) 2. Current (within the past year) alcohol or drug use disorder as defined by DSM 5 (MINI 7.0.2) at Screening (V1) 3. Significant suicide risk as defined by (1) suicidal ideation as endorsed on items 4 or 5 on the C-SSRS within the past year, at Screening or at Baseline, or; (2) suicidal behaviors within the past year, or; (3) clinical assessment of significant suicidal risk during subject interview 4. Other personal circumstances and behaviour judged to be incompatible with establishment of rapport or safe exposure to psilocybin General Medical Exclusion Criteria: 5. Women who are pregnant, nursing, or planning a pregnancy. Women and men of child bearing potential and who are sexually active must agree to use an acceptable contraceptive method throughout their participation in the study. Women of child bearing potential must have a negative urine pregnancy test at Screening (V1) and Baseline (V2) 6. Cardiovascular conditions: recent stroke (\<1 year from signing of ICF), recent myocardial infarction (\<1 year from signing of ICF), uncontrolled hypertension (blood pressure \>140/90) or clinically significant arrhythmia within 1 year of signing the ICF 7. Uncontrolled or insulin dependent diabetes 8. Seizure disorder 9. Positive urine drug screen for illicit drugs or drugs of abuse at V1 and V2. Any positive urine drug test will be reviewed with participants to determine the pattern of use and eligibility will be determined at the investigator's discretion in conjunction with the medical monitor 10. Current enrollment in any investigational drug or device study or participation in such within 30 days of Screening. 11. Abnormal and clinically significant results on the physical examination, vital signs, ECG, or laboratory tests at Screening (V1) that in the investigator's opinion may consistute a risk for an individual who is explosed to psilocybin. This includes platelets below 50,000 platelets per cubic millimeter of blood, liver function tests three times the upper limit of normal, creatine two times above the normal range. Clinically significant abnormal electrolytes or low hemoglobin (below 8 g/L) should be corrected and rechecked 12. Any other clinically significant cardiovascular, pulmonary, gastrointestinal, hepatic, renal or any other major concurrent illness that, in the opinion of the investigator, may interfere with the interpretation of the study results or constitute a health risk for the participant if he/she takes part in the study 13. Use of psychedelics, including psilocybin but excluding medical marijuana, within the past 12 months and use of psychedelics during the current episode of depression 14. Concurrent or recent chemotherapy or radiation therapy, that impairs general level of phsyical functioning.

Where

1 study site

FacilityCityRegionCountry
Maryland Oncology Hematology PARockvilleMarylandUnited States

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

Before you do, the preparation checklist lists what a site will ask you on a first call and what is worth asking them. It is free and collects nothing.

NCT04593563 on ClinicalTrials.gov →

Last updated in the registry 2021-10-15. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits

Substance

Recruiting in