A Study of RO4917838 (Bitopertin) in Patients With Persistent, Predominant Negative Symptoms of Schizophrenia (WN25309)
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 information
- 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.
Recruitment & locations
CompletedCarson, 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
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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