A Study of RO4917838 (Bitopertin) in Patients With Sub-optimally Controlled Symptoms of Schizophrenia (WN25306)
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 119 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
- 597
- 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
- NCT01235585
- Official title
Show the full official title
Phase III, Multi-center, Randomized, 12-week, Double-blind, Parallel-group, Placebo-controlled Study to Evaluate the Efficacy and Safety of RO4917838 in Patients With Sub-optimally Controlled Symptoms of Schizophrenia Treated With Antipsychotics Followed by a 40-week Double-blind, Parallel-group, Placebo-controlled Treatment Period.
Recruitment & locations
CompletedCarson, United States · Garden Grove, United States · Long Beach, United States
92 more locations
- Oceanside, United States
- San Diego, United States
- 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
- 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
- Bothell, United States
- Salvador, Brazil
- Goiânia, Brazil
- Belo Horizonte, Brazil
- Curitiba, Brazil
- Rio de Janeiro, Brazil
- Pelotas, Brazil
- Porto Alegre, Brazil
- Itapira, Brazil
- São Paulo, Brazil
- Calgary, Canada
- Medicine Hat, Canada
- Vancouver, Canada
- Halifax, Canada
- Burlington, Canada
- Hamilton, Canada
- Mississauga, Canada
- Montreal, Canada
- 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
- Trnava, 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
- Kocaeli, Türkiye
- Manisa, Türkiye
- Mersin, Türkiye
- Dnipropetrovsk, Ukraine
- Donetsk, Ukraine
- Glevakha Kyviv Region, Ukraine
- Kharkiv, Ukraine
- Kyiv, Ukraine
- Lviv, Ukraine
- Odesa, Ukraine
- Vinnytsia, Ukraine
- Türkiye
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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