Not recruitingISRCTN33909010

A phase 3 randomised placebo- and active comparator-controlled, clinical trial to study the safety and efficacy of two doses of lurasidone HCL in acutely psychotic patients with schizophrenia

Research studyAges 18+Multiple countries

The study in practice

Understand this study

This study is for people with schizophrenia. Listed age limits: from 18 years. Other eligibility criteria apply.

A point to clarify

This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

Study clarity

Study start dateNot clearly listed

Recruitment status: Not recruiting
Enrollment listed in the registry: Not clearly listed
Sponsor: Dainippon Sumitomo Pharma America Inc. (USA)
Sponsor type: Pharmaceutical company
Study type: Other
Intervention type: Other / unclear
Study phase: Not clearly listed
Locations: United Kingdom, Bulgaria, Colombia, ...
Age range: Over 18 Years
Official registry ID: ISRCTN33909010
Official title: Show the full official title
A phase 3 randomised placebo- and active comparator-controlled, clinical trial to study the safety and efficacy of two doses of lurasidone HCL in acutely psychotic patients with schizophrenia

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Not recruiting

United Kingdom · Bulgaria · Colombia

5 more locations

A listed location does not confirm current availability.

FAQ

Who is behind this study?

The study sponsor is Dainippon Sumitomo Pharma America Inc. (USA), a pharmaceutical company.

Who can participate?

This study is for people with schizophrenia. Listed age limits: from 18 years. Other eligibility criteria apply.

Is this study still recruiting?

The registry lists this study as not recruiting.

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