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CompletedNCT01192906

A Study of RO4917838 (Bitopertin) in Patients With Persistent, Predominant Negative Symptoms of Schizophrenia (WN25309)

Medication studyAges 18+Multiple countries
The study in practice

Understand this study

Who was this study for?

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

Listed locations
Carson and 112 more locationsSee all locations and recruitment
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Study clarity

Study information

Study start dateDecember 2010
Recruitment status
Completed
Enrollment listed in the registry
624
Sponsor
Hoffmann-La Roche
Sponsor type
Unknown or unclear
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United States, Canada, Brazil, ...
Age range
Over 18 Years
Official registry ID
NCT01192906
Official title
Show the full official title

A Phase III, Multi-center, Randomized, 24 Week, Double-blind, Parallel-group, Placebo-controlled Study to Evaluate Efficacy and Safety of RO4917838 in Stable Patients With Persistent, Predominant Negative Symptoms of Schizophrenia Treated With Antipsychotics Followed by a 28 Week, Double-blind Treatment Period.

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Recruitment & locations

Completed

Carson, United States · Oceanside, United States · San Diego, United States

89 more locations
  • Hartford, United States
  • Norwalk, United States
  • North Miami, United States
  • Atlanta, United States
  • Chicago, United States
  • Hoffman Estates, United States
  • Joliet, United States
  • Lake Charles, United States
  • Shreveport, United States
  • St Louis, United States
  • Omahac, United States
  • Cedarhurst, United States
  • Jamaica, United States
  • Rochester, United States
  • Allentown, United States
  • Norristown, United States
  • Philadelphia, United States
  • Salvador, Brazil
  • Goiânia, Brazil
  • Belo Horizonte, Brazil
  • Curitiba, Brazil
  • Rio de Janeiro, Brazil
  • Pelotas, Brazil
  • Porto Alegre, Brazil
  • São Paulo, Brazil
  • Calgary, Canada
  • Medicine Hat, Canada
  • Vancouver, Canada
  • Victoria, Canada
  • Halifax, Canada
  • Burlington, Canada
  • Hamilton, Canada
  • Mississauga, Canada
  • Montreal, Canada
  • Verdun, Canada
  • San Miguel, Chile
  • Santiago, Chile
  • Valdivia, Chile
  • Berlin, Germany
  • Bochum, Germany
  • Cologne, Germany
  • Freiburg im Breisgau, Germany
  • Hamburg, Germany
  • München, Germany
  • Nuremberg, Germany
  • Daugovpils, Latvia
  • Jelgava, Latvia
  • Liepāja, Latvia
  • Kaunas, Lithuania
  • Šilutė, Lithuania
  • Vilnius, Lithuania
  • Assen, Netherlands
  • Groningen, Netherlands
  • Choroszcz, Poland
  • Kielce, Poland
  • Lublin, Poland
  • Piekary Śląskie, Poland
  • Skorzewo, Poland
  • Tuszyn, Poland
  • Warsaw, Poland
  • Bojnice, Slovakia
  • Bratislava, Slovakia
  • Rimavská Sobota, Slovakia
  • Svidník, Slovakia
  • Barcelona, Spain
  • Madrid, Spain
  • Oviedo, Spain
  • Salamanca, Spain
  • Zamora, Spain
  • Hualian Town, Taiwan
  • Kaohsiung City, Taiwan
  • Taichung, Taiwan
  • Tainan, Taiwan
  • Tainan County, Taiwan
  • Taipei, Taiwan
  • Ankara, Türkiye
  • Diyarbakır, Türkiye
  • Gaziantep, Türkiye
  • Istanbul, Türkiye
  • Manisa, Türkiye
  • Dnipropetrovsk, Ukraine
  • Donetsk, Ukraine
  • Glevakha Kyviv Region, Ukraine
  • Kharkiv, Ukraine
  • Kyiv, Ukraine
  • Lviv, Ukraine
  • Odesa, Ukraine
  • Vinnytsia, Ukraine
  • Türkiye
FAQ

Questions about this study

Who is behind this study?

The study sponsor is Hoffmann-La Roche.

Did this study involve medication?

Yes. The study involved medication, including Placebo and bitopertin [RO4917838].

Who was this study for?

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

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