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CompletedEUCTR 2018-002901-68

Double-blind, controlled, randomized phase 2 study of efficacy, safety, pharmacokinetics and pharmacodynamics of a daily oral administration of MAP4343 during 6 weeks in antidepressant-non responde...

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Historical research recordFranceDepression
The study in practice

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What did researchers investigate?

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

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Study clarity

Study information

Study start dateNot clearly listed
Recruitment status
Completed
Enrollment listed in the registry
Not clearly listed
Sponsor
MAPREG
Sponsor type
Unknown or unclear
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
France
Age range
Not clearly listed
Official registry ID
EUCTR 2018-002901-68
Official title
Show the full official title

Double-blind, controlled, randomized phase 2 study of efficacy, safety, pharmacokinetics and pharmacodynamics of a daily oral administration of MAP4343 during 6 weeks in antidepressant-non responde...

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Recruitment & locations

Completed

France

Registry details
Historical country statuses
FAQ

Questions about this study

Who is behind this study?

The study sponsor is MAPREG.

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