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CompletedNCT01626885

A Long-Term Study of MP-214 in Patients With Receiving Multiple Drugs Schizophrenia

Medication studyAges 20–64Japan
The study in practice

Understand this study

Who was this study for?

This study was for people with schizophrenia. Listed age limits: 20 years to 64 years. Other eligibility criteria applied.

Listed locations
KurayoshiSee all locations and recruitment
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 dateMay 2012
Recruitment status
Completed
Enrollment listed in the registry
42
Sponsor
Tanabe Pharma Corporation
Sponsor type
Pharmaceutical company
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
Japan
Age range
From 20 Years to 64 Years
Official registry ID
NCT01626885
Official title
Show the full official title

A Long-Term Study of MP-214 in Patients With Receiving Multiple Drugs Schizophrenia

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Recruitment & locations

Completed

Kurayoshi

FAQ

Questions about this study

Who is behind this study?

The study sponsor is Tanabe Pharma Corporation, a pharmaceutical company.

Did this study involve medication?

Yes. The study involved medication, including MP-214.

Who was this study for?

This study was for people with schizophrenia. Listed age limits: 20 years to 64 years. Other eligibility criteria applied.

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