- Trials with a EudraCT protocol (11)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (10)
11 result(s) found for: Psilocybine.
Displaying page 1 of 1.
EudraCT Number: 2021-006233-19 | Sponsor Protocol Number: COMP401 | Start Date*: 2023-01-20 |
Sponsor Name:COMPASS Pathfinder Limited | ||
Full Title: Efficacy and safety of COMP360 psilocybin therapy in anorexia nervosa: a proof-of-concept study | ||
Medical condition: Anorexia Nervosa (AN) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003382-34 | Sponsor Protocol Number: NeuroPharm_EPOCH | Start Date*: 2019-06-17 | |||||||||||||||||||||
Sponsor Name:NeuroPharm | |||||||||||||||||||||||
Full Title: Prophylactic effects of psilocybin on chronic cluster headache: an open-label clinical trial and neuroimaging study. | |||||||||||||||||||||||
Medical condition: Chronic cluster headache. | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000041-40 | Sponsor Protocol Number: P131 | Start Date*: 2022-02-22 |
Sponsor Name:Maastricht University | ||
Full Title: A study to investigate the effects of repeated low doses of psilocybin and ketamine on cognitive and emotional dysfunctions in Parkinson’s disease and to understand its mechanism of action | ||
Medical condition: Parkinson's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-003381-21 | Sponsor Protocol Number: RAFAEL | Start Date*: 2023-09-11 |
Sponsor Name:Psyon, s.r.o. | ||
Full Title: Regression of atherosclerosis induced by life changing experience with psilocybin | ||
Medical condition: Ischemic Heart Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004579-37 | Sponsor Protocol Number: MZ12-PCP-PalenicekTomas-A | Start Date*: 2014-06-18 |
Sponsor Name:National Institute of Mental Health | ||
Full Title: Animal and human serotonergic model of schizophrenia: validity evaluated by qEEG and fMRI | ||
Medical condition: Inclusion criteria: a) Men and women at age between 28 and 65 years b) healthy volunteers with negative psychiatric history (severe mental illnesses that meet the criteria of ICD 10 F0.X - F99.X) ... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002909-10 | Sponsor Protocol Number: P137 | Start Date*: 2022-10-24 |
Sponsor Name:Maastricht University | ||
Full Title: THE IMPACT OF PSILOCYBIN ON PAIN IN FIBROMYALGIA PATIENTS AND HEALTHY VOLUNTEERS: A MULTICENTER TRIAL | ||
Medical condition: Fibromyalgia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005037-32 | Sponsor Protocol Number: PSIKET_002CZE | Start Date*: 2021-09-22 | |||||||||||
Sponsor Name:Národní ústav duševního zdraví | |||||||||||||
Full Title: Psilocybin - a strategy of rapid antidepressant response in depression comorbid with cancer, a randomized double-blind study with the possibility of entering open extension. | |||||||||||||
Medical condition: Depressive disorder comorbid with cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002577-22 | Sponsor Protocol Number: COMP003 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:COMPASS Pathfinder, Limited | ||||||||||||||||||
Full Title: The safety and efficacy of psilocybin as an adjunctive therapy in participants with treatment-resistant depression | ||||||||||||||||||
Medical condition: treatment resistant depression | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004480-31 | Sponsor Protocol Number: PSIKET_001CZE | Start Date*: 2020-07-14 |
Sponsor Name:Národní ústav duševního zdraví | ||
Full Title: Psilocybin versus ketamine – fast acting antidepressant strategies in treatment-resistant depression | ||
Medical condition: The study will include 60 patients with pharmaco-resistant depression (30 male, 30 female, aged 18–65). The basic inclusion criterion is the diagnosis of pharmaco-resistant moderate to severe depre... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: CZ (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006200-33 | Sponsor Protocol Number: CLA-PSY-201 | Start Date*: 2022-09-22 | |||||||||||
Sponsor Name:Clairvoyant Therapeutics Inc. | |||||||||||||
Full Title: A 24-Week, Multicentre, Randomised, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2 Clinical Trial to Evaluate Efficacy and Safety of Psilocybin-Assisted Psychotherapy in Adults with A... | |||||||||||||
Medical condition: Alcohol use disorder (AUD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002790-94 | Sponsor Protocol Number: 200828 | Start Date*: 2020-09-16 | |||||||||||
Sponsor Name:SLSO | |||||||||||||
Full Title: The Effect of Psilocybin on MDD Symptom Severity and Synaptic Density – A Single Dose Randomized, Double Blind, Placebo-Controlled Phase 2 Positron Emission Tomography Study | |||||||||||||
Medical condition: Major Depressive Disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
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