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CompletedEUCTR 2010-024198-38

A long-term, open-label, flexible-dose, extension study evaluating the safety and tolerability of Lu AA21004 (15 and 20 mg/day) in patients with Major Depressive Disorder

This historical record does not confirm current site availability.

Historical research recordMultiple countriesDepression
The study in practice

Understand this study

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.

Who was this study for?

This study was for people with depression. Other eligibility criteria applied.

Listed locations
Belgium · Estonia and 4 more locations
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.

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Study clarity

Study information

Study start dateNot clearly listed
Recruitment status
Completed
Enrollment listed in the registry
300
Sponsor
H. Lundbeck A/S
Sponsor type
Unknown or unclear
Study type
Drug
Intervention type
Drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
Belgium, Estonia, Finland, ...
Age range
Not clearly listed
Official registry ID
EUCTR 2010-024198-38
Official title
Show the full official title

A long-term, open-label, flexible-dose, extension study evaluating the safety and tolerability of Lu AA21004 (15 and 20 mg/day) in patients with Major Depressive Disorder

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Recruitment & locations

Completed

Belgium · Estonia · Finland

3 more locations
  • Latvia
  • Lithuania
  • Sweden
Registry details
Historical country statuses

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is H. Lundbeck A/S.

Who was this study for?

This study was for people with depression. Other eligibility criteria applied.

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