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Completed

NCT Number: NCT04959253

Psilocybin in Depression Resistant to Standard Treatments

A single centre clinical trial to evaluate the feasibility, safety and efficacy of psilocybin, given under supportive conditions, in a randomised, blinded design in adult participants with treatment resistant major depressive disorder. The primary objective is to evaluate feasibility by measuring recruitment rates, dropout rates and by estimating the variance of the primary outcome measure (MADRS).

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Key information

Age range

25 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Clinical Research Facility, King's College Hospital

London, SE5 9RS, United Kingdom

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 25 - 80 years
  • Fluent in the English language
  • Fulfil Diagnostic and Statistical Manual of Mental Disorders (5th Edition) (DSM-5) criteria for a primary diagnosis of current single or recurrent episodes of MDD of at least moderate severity but without psychotic features as defined on the MINI 7.0. Positive and primary diagnoses on the MINI 7.0 will be subject to confirmation at clinical interview by a psychiatrist.
  • 17-item HAM-D score ≥ 14.
  • Have failed to respond to 2 or more antidepressants prescribed at the minimum effective dose for at least 6 weeks OR at least 1 antidepressant prescribed at the minimum effective dose for at least 6 weeks AND a course of evidence-based psychotherapy given for at least 6 sessions.
  • For those aged ≥ 60 years, the first episode of depression must have started prior to their 60th birthday.

Exclusion criteria

  • Diagnosis of bipolar disorder (defined as meeting DSM-5 criteria for bipolar 1 or bipolar 2) on the MINI 7.0. Positive diagnoses on the MINI will be subject to confirmation at clinical interview by a psychiatrist.
  • Diagnosis of psychotic disorder (defined as meeting DSM-5 criteria for any psychotic disorder) on the MINI 7.0, EXCEPT substance/medication induced psychotic disorder where the duration was limited to the acute period of direct intoxication with the substance/medication. Positive diagnoses on the MINI will be subject to confirmation at clinical interview by a psychiatrist.
  • Diagnosis of drug or alcohol dependence syndrome (defined as meeting DSM-5 criteria for any dependence syndrome) on the MINI 7.0. Positive diagnoses on the MINI will be subject to confirmation at clinical interview by a psychiatrist.
  • Diagnosis of any personality disorder (defined as meeting DSM-5 criteria for any personality disorder) based on clinical interview and the MINI 7.0. Positive diagnoses on the MINI will be subject to confirmation at clinical interview by a psychiatrist.
  • Diagnosis of any dementia (defined as meeting DSM-5 criteria for any dementia disorder) based on clinical interview by a psychiatrist.
  • Personal history of a ≥ 1 suicide attempt in the past year requiring hospitalization, defined using the CSSRS (Q6 (past year) = "y") and clinical interview with a psychiatrist.
  • Other personal circumstances and behaviour judged to be incompatible with establishment of rapport or safe exposure to psilocybin.
  • Depression secondary to other medical conditions
  • Medical diagnosis incompatible with psilocybin treatment
  • Inability to provide a screening blood sample, urine sample or electrocardiogram.
  • Biochemical abnormalities (defined as falling outside the normal reference range) as evaluated by a full blood count, full biochemistry profile and thyroid function tests. Biochemical abnormalities must also be determined as clinically significant by a medical doctor to fulfil the criterion for exclusion.
  • Electrocardiographic abnormalities, defined as any abnormality that is not normal sinus rhythm and determined as clinically significant by a medical doctor.
  • Women of child bearing potential not using adequate contraception.
  • Pregnant or breast-feeding women.
  • Those unable to give informed consent.
  • Non-registration with a GP or failure to consent to sharing of the GP summary care record and any psychiatric assessments held.
  • Those enrolled in another drug trial
  • Hypersensitivity to the IMP or to any of the excipients or placebo

Exclusions for Pre-Existing Medical Conditions

Participants will be excluded if they have a current diagnosis of ≥1 of:

  • Uncontrolled diabetes
  • Hypertension (defined as a systolic blood pressure ≥ 160mm/Hg or a diastolic blood pressure ≥ 100mm/Hg on three separate readings). All readings of systolic blood pressure ≥ 140mm/Hg or diastolic blood pressure ≥ 90mm/Hg will be reviewed by a clinician. Hypertension ascertained prior to dosing will be subject to clinical confirmation via collateral information from the GP or other source.
  • Cardiac failure, defined as class IV of the New York Heart Association classification
  • Renal failure, defined as ≥ stage 4 (GFR ≤ 29mL/min)
  • Liver failure, defined as a clinical diagnosis of liver fibrosis, cirrhosis of the liver, liver failure or advanced liver disease.
  • Any cardiac arrhythmia, except atrial fibrillation.
  • Any form of epilepsy

Past diagnosis of ≥1 of:

  • Cerebrovascular accident or intracerebral trauma.
  • Myocardial infarction within 1 year prior to the screening visit.

Treatment and study plan

Psilocybin assisted therapy

Combination Product

A package of psychological therapy and a single dosing session of psilocybin.

Placebo assisted therapy

Combination Product

A package of psychological therapy and a single dosing session of placebo.

Primary outcomes

  1. Recruitment rates

    Time frame: From opening to closing of trial recruitment period

    Recruitment rates to the trial

  2. Dropout rates

    Time frame: From time of first enrollment until last participant last visit

    Dropout rates in the trial

  3. Montgomery Asberg Depression Rating Scale (MADRS)

    Time frame: 3 weeks from baseline

    The variance in the MADRS between groups

Secondary outcomes

  1. Montgomery Asberg Depression Rating Scale (MADRS)

    Time frame: 3 weeks from baseline

    The change in the Montgomery-Asberg Depression Rating Scale total score from the Baseline Visit (V2 - 1 day prior to treatment) to Week 3 after treatment (V6). Higher scores mean worse depression. Lowest score is 0. Highest score is 60.

  2. Montgomery Asberg Depression Rating Scale (MADRS)

    Time frame: 6 weeks from baseline

    The change in the Montgomery-Asberg Depression Rating Scale total score from the Baseline Visit (V2 - 1 day prior to treatment) to Week 3 after treatment (V6). Higher scores mean worse depression. Lowest score is 0. Highest score is 60.

  3. Time to event measures

    Time frame: At any point from baseline (day 0) visit until 6-week follow-up

    Restart antidepressant medication for any reason, restart medication for continuing depressive symptoms or relapse from a previously recovered state (clinical judgement, supported by the QIDS-SR-16). Participants who withdraw from the study will be censored from the time to event analysis.

Other outcomes

  1. Work and Social Adjustment Scale (WSAS)

    Time frame: Week 6

    Change from baseline in the WSAS at week 6. Higher scores mean worse impairment. Lowest score = 0. Highest score = 40.

  2. Quick Inventory of Depressive Symptoms (QIDS-SR-16)

    Time frame: Week 3

    Change from baseline in the QIDS-SR-16 at week 3. Higher scores mean worse depression symptoms. Minimum score = 0. Maximum score = 27.

  3. Generalised Anxiety Disorder 7 (GAD-7)

    Time frame: Week 3

    Change from baseline in the GAD-7 at week 3. Higher scores mean worse symptoms. Lowest score = 0. Highest score = 21.

Sponsors and collaborators

Lead sponsor

King's College London

Other

Collaborators

  • South London and Maudsley NHS Foundation Trust

Registry information

Official study title

A Randomised, Placebo Controlled Trial of Psilocybin in Treatment Resistant Depression: A Feasibility Study

Acronym: PsiDeR

Important dates

Study start
2021
Primary completion
2024
Study completion
2024
First posted
Jul 13, 2021
Registry last updated
Aug 28, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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