Lurasidone Safety and Efficacy in Children and Adolescents With Schizophrenia
About this title
Read the official source — NCT01911429Researchers compared Lurasidone 40 mg, Lurasidone 80 mg and placebo to find out how the approaches affected psychotic symptoms in young people with schizophrenia.
Understand this study
What did researchers investigate?
Researchers compared Lurasidone 40 mg, Lurasidone 80 mg and placebo to find out how the approaches affected psychotic symptoms in young people with schizophrenia.
Who was this study for?
This study was for people with schizophrenia. Listed age limits: 13 years to 17 years. Other eligibility criteria applied.
- Listed locations
- Dothan and 89 more locationsSee all locations and recruitment
- Study phase
- Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Study information
- Recruitment status
- Completed
- Enrollment listed in the registry
- 327
- Sponsor
- Sumitomo Pharma America, Inc.
- Sponsor type
- Pharmaceutical company
- Study type
- Drug
- Intervention type
- Drug
- Study phase
- Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
- Locations
- United States, France, United Kingdom, ...
- Age range
- From 13 Years to 17 Years
- Official registry ID
- NCT01911429
- Official title
Show the full official title
A 6-Week Randomized, Parallel, Double-Blind, Placebo-Controlled, Fixed-Dose, Multicenter Study To Evaluate The Efficacy and Safety of Lurasidone in Adolescent Subjects With Schizophrenia
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Explore recruiting studiesRecruitment & locations
Dothan, United States · Anaheim, United States · Bakersfield, United States
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- Brussels, Belgium
- Rousse, Bulgaria
- Sofia, Bulgaria
- Targovishte, Bulgaria
- Varna, Bulgaria
- Barranquilla, Colombia
- Bello, Colombia
- Bogotá, Colombia
- Nantes, France
- Nice, France
- Budapest, Hungary
- Gyula, Hungary
- Lembah Pantai, Malaysia
- Culiacán, Mexico
- Monterrey, Mexico
- Daveo City, Philippines
- Iloilo City, Philippines
- Mandaluyong, Philippines
- Quezon City, Philippines
- Torun, Poland
- Tyniec Mały, Poland
- Warsaw, Poland
- Caguas, Puerto Rico
- Ponce, Puerto Rico
- San Juan, Puerto Rico
- Bucharest, Romania
- Iași, Romania
- Timișoara, Romania
- Lipetsk, Russia
- Saint Petersburg, Russia
- Saratov, Russia
- Tomsk, Russia
- Velikiy Novgorod, Russia
- Yekaterinburg, Russia
- Incheon, South Korea
- Jeonju, South Korea
- Seoul, South Korea
- Torremolinos, Spain
- Barcelona, Spain
- Ivano-Frankivsk, Ukraine
- Kharkiv, Ukraine
- Kherson,Vil. Stepanivka, Ukraine
- Kyiv, Ukraine
- Lviv, Ukraine
- Odesa, Ukraine
- Poltava, Ukraine
- Ternopil, Ukraine
- Vinnytsia, Ukraine
- Aberdeen, United Kingdom
- Birmingham, United Kingdom
- Edinburgh, United Kingdom
- Russia
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Questions about this study
What did researchers investigate?
Researchers compared Lurasidone 40 mg, Lurasidone 80 mg and placebo to find out how the approaches affected psychotic symptoms in young people with schizophrenia.
Who is behind this study?
The study sponsor is Sumitomo Pharma America, Inc., a pharmaceutical company.
Did this study involve medication?
Yes. The study involved medication, including Lurasidone 40 mg, Lurasidone 80 mg and Placebo 40 or 80 mg.
Who was this study for?
This study was for people with schizophrenia. Listed age limits: 13 years to 17 years. Other eligibility criteria applied.
