A phase three randomised, placebo-controlled, clinical trial to study the safety and efficacy of three doses of lurasidone hydrochloride (HCl) in acutely psychotic patients with schizophrenia
Research studyAges 18+Multiple countries
The study in practice
Understand this study
Who could participate?
This study is for people with schizophrenia. Listed age limits: from 18 years. Other eligibility criteria apply.
Listed locations
United Kingdom · France and 6 more locations
Compensation
Payment and expense reimbursement have not been verified.
What to know before participating
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
Things to check before joining
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 States, France, United Kingdom, ...
Age range
Over 18 Years
Official registry ID
ISRCTN16838597
Official title
Show the full official title
A phase three randomised, placebo-controlled, clinical trial to study the safety and efficacy of three doses of lurasidone hydrochloride (HCl) in acutely psychotic patients with schizophrenia
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Recruitment & locations
Not recruiting
United Kingdom · France · India
5 more locations
Malaysia
Romania
Russia
Ukraine
United States
A listed location does not confirm current availability.
FAQ
Questions about this study
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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