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CompletedNCT00728195

JNJ-37822681 or placebo for schizophrenia

About this titleRead the official source — NCT00728195

This study evaluated the safety and effectiveness of JNJ-37822681 for people with schizophrenia.

Medication studyAges 18–65Multiple countries
The study in practice

Understand this study

What did researchers investigate?

This study evaluated the safety and effectiveness of JNJ-37822681 for people with schizophrenia.

Who was this study for?

This study was for people with schizophrenia. Listed age limits: 18 years to 65 years. Other eligibility criteria applied.

Listed locations
Burgas and 44 more locationsSee all locations and recruitment
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.

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Study clarity

Study information

Study start dateNovember 2008
Recruitment status
Completed
Enrollment listed in the registry
498
Sponsor
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Sponsor type
Pharmaceutical company
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
Bulgaria, Estonia, Lithuania, ...
Age range
From 18 Years to 65 Years
Official registry ID
NCT00728195
Official title
Show the full official title

A Randomized, Double-Blind, Placebo- and Active-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of 3 Fixed Doses of JNJ-37822681 Administered Twice Daily in Subjects With Schizophrenia

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Recruitment & locations

Completed

Burgas, Bulgaria · Pazardzhik, Bulgaria · Radnevo, Bulgaria

43 more locations
  • Rousse, Bulgaria
  • Sofia, Bulgaria
  • Tallinn, Estonia
  • Tartu, Estonia
  • Kaunas, Lithuania
  • Vilnius, Lithuania
  • Johor Bahru, Malaysia
  • Kuala Lumpur, Malaysia
  • Kuching, Malaysia
  • Arad, Romania
  • Brasov, Romania
  • Bucharest, Romania
  • Jebel, Romania
  • Oradea, Romania
  • Sibiu, Romania
  • Tg Mures, Romania
  • Ekaterinburg Na, Russia
  • Moscow, Russia
  • Moscow Russia, Russia
  • N Novgorod Na, Russia
  • Saint Petersburg, Russia
  • Samara, Russia
  • Saratov, Russia
  • Tomsk Na, Russia
  • Yaroslavl, Russia
  • Cape Town, South Africa
  • Centurion Gauteng, South Africa
  • Pretoria, South Africa
  • Gwangju, South Korea
  • Gyeongsangnam-Do, South Korea
  • Incheon, South Korea
  • Seoul, South Korea
  • Hualien City, Taiwan
  • Kaohsiung City, Taiwan
  • Taipei, Taiwan
  • Dnipropetrovsk, Ukraine
  • Donetsk, Ukraine
  • Kharkiv, Ukraine
  • Kherson, Ukraine
  • Kiev, Ukraine
  • Odesa, Ukraine
  • Simferopol, Ukraine
  • Russia
FAQ

Questions about this study

What did researchers investigate?

This study evaluated the safety and effectiveness of JNJ-37822681 for people with schizophrenia.

Who is behind this study?

The study sponsor is Johnson & Johnson Pharmaceutical Research & Development, L.L.C., a pharmaceutical company.

Did this study involve medication?

Yes. The study involved medication, including JNJ-37822681, Olanzapine and Placebo.

Who was this study for?

This study was for people with schizophrenia. Listed age limits: 18 years to 65 years. Other eligibility criteria applied.

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