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CompletedEUCTR 2008-001441-26

A randomised, double-blind, parallel-group, fixed dose study exploring the efficacy and safety of Lu AE58054 as augmentation therapy to risperidone in patients with schizophrenia.

This historical record does not confirm current site availability.

Historical research recordMultiple countries
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 schizophrenia. Other eligibility criteria applied.

Listed locations
Belgium · France and 3 more locations
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
120
Sponsor
H. Lundbeck A/S
Sponsor type
Unknown or unclear
Study type
Drug
Intervention type
Drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
France, Belgium, Germany, ...
Age range
Not clearly listed
Official registry ID
EUCTR 2008-001441-26
Official title
Show the full official title

A randomised, double-blind, parallel-group, fixed dose study exploring the efficacy and safety of Lu AE58054 as augmentation therapy to risperidone in patients with schizophrenia.

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Recruitment & locations

Completed

Belgium · France · Germany

2 more locations
  • Italy
  • Poland
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 schizophrenia. Other eligibility criteria applied.

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