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TerminatedEUCTR 2007-001097-90

A one-year multinational, multi-centre, randomised, double-blind, parallel-group, fixed-dose, bifeprunox study combining a 12 week placebo-controlled, quetiapine-referenced phase with a 12-month qu...

This historical record does not confirm current site availability.

Historical research recordBulgaria + GreeceSchizophrenia
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
Bulgaria · Greece
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.

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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
450
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
Bulgaria, Greece
Age range
Not clearly listed
Official registry ID
EUCTR 2007-001097-90
Official title
Show the full official title

A one-year multinational, multi-centre, randomised, double-blind, parallel-group, fixed-dose, bifeprunox study combining a 12 week placebo-controlled, quetiapine-referenced phase with a 12-month qu...

Recruitment & locations

Terminated

Bulgaria · Greece

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.

Is this study still recruiting?

The historical registry lists this study as terminated.

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