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CompletedEUCTR 2010-022257-41

A Multinational, Randomized, Double-Blind, Placebo-Controlled, Dose Ranging Study to Assess the Efficacy and Safety of Lu AA21004 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
Finland · Germany and 2 more locations
Study phase
Phase 2 / Phase 3This study spans more than one phase, so it may combine goals such as safety, dosing, and early effectiveness.
Study clarity

Study information

Study start dateNot clearly listed
Recruitment status
Completed
Enrollment listed in the registry
615
Sponsor
Takeda Global Research and Development Centre (Europe) Ltd.
Sponsor type
Other organization
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 2, Phase 3This study spans more than one phase, so it may combine goals such as safety, dosing, and early effectiveness.
Locations
Finland, Germany, Latvia, ...
Age range
Not clearly listed
Official registry ID
EUCTR 2010-022257-41
Official title
Show the full official title

A Multinational, Randomized, Double-Blind, Placebo-Controlled, Dose Ranging Study to Assess the Efficacy and Safety of Lu AA21004 in Patients with Major Depressive Disorder

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Recruitment & locations

Completed

Finland · Germany · Latvia

1 more locations
  • Romania
Registry details
Historical country statuses
FAQ

Questions about this study

Who is behind this study?

The study sponsor is Takeda Global Research and Development Centre (Europe) Ltd.

Who was this study for?

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

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