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TerminatedEUCTR 2021-006200-33

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...

This historical record does not confirm current site availability.

Historical research recordFinlandAddiction
The study in practice

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What is this study about?

This EU register entry describes an interventional medicine trial, designed to assign participants a study treatment. The protocol sets out the treatment, eligibility criteria and assessments. Check the source details below for country statuses and any transfer to CTIS.

Listed locations
Finland
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.

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What to know before participating

A point to clarify

This is historical registry information. What is the current study status and protocol?

Study clarity

Things to check before joining

Study start dateNot clearly listed
Recruitment status
Terminated
Enrollment listed in the registry
160
Sponsor
Clairvoyant Therapeutics Inc.
Sponsor type
Biotech company
Study type
Drug
Intervention type
Drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
Finland
Age range
Not clearly listed
Official registry ID
EUCTR 2021-006200-33
Official title
Show the full official 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...

Recruitment & locations

Terminated

Finland

Registry details
Historical country statuses

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is Clairvoyant Therapeutics Inc.

Is this study still recruiting?

The historical registry lists this study as terminated.

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