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CompletedEUCTR 2016-000061-23

A 12-Week, Open-Label Extension Study of Lurasidone (SM-13496) in Subjects with Schizophrenia

This historical record does not confirm current site availability.

Historical research recordPoland + Slovakia
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
Poland · Slovakia
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Study clarity

Study information

Study start dateNot clearly listed
Recruitment status
Completed
Enrollment listed in the registry
283
Sponsor
Sunovion Pharmaceuticals Inc.
Sponsor type
Other organization
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
Poland, Slovakia
Age range
Not clearly listed
Official registry ID
EUCTR 2016-000061-23
Official title
Show the full official title

A 12-Week, Open-Label Extension Study of Lurasidone (SM-13496) in Subjects with Schizophrenia

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Recruitment & locations

Completed

Poland · Slovakia

Registry details
Historical country statuses
FAQ

Questions about this study

Who is behind this study?

The study sponsor is Sunovion Pharmaceuticals Inc.

Who was this study for?

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

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