A Study Evaluating Lurasidone for The Treatment of Schizophrenia or Schizoaffective Disorder in Subjects Switched From Other Antipsychotic Agents
Launched by SUMITOMO PHARMA AMERICA, INC. · Jun 11, 2010
Trial Information
Current as of July 21, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Subject ≥ 18 years of age.
- • Subject meets DSM-IV criteria for a primary diagnosis of schizophrenia or schizoaffective disorder.
- • Subject must be judged by the investigator to be an appropriate candidate for switching current antipsychotic medication due to insufficient efficacy and/or safety or tolerability concerns.
- Exclusion Criteria:
- • Presence of an Axis I or Axis II disorder other than schizophrenia or schizoaffective disorder that is the primary focus of treatment prior to screening.
- • Subject has experienced persistent lack of improvement in psychotic symptoms despite adequate trials (at least 6 weeks at standard doses), of two or more antipsychotic agents in the 12 months prior to screening.
- • Subject is considered by the investigator to be at imminent risk of suicide or harm to self, others, or property. Subject has suicidal ideation at baseline or has attempted suicide within 90 days prior to randomization (even without hospitalization).
About Sumitomo Pharma America, Inc.
Sumitomo Pharma America, Inc. is a leading biopharmaceutical company dedicated to the research, development, and commercialization of innovative therapies that address unmet medical needs. As a subsidiary of Sumitomo Pharma Co., Ltd., the company leverages its global expertise and cutting-edge scientific advancements to advance treatments in various therapeutic areas, including neuroscience, oncology, and infectious diseases. Committed to enhancing patient outcomes, Sumitomo Pharma America, Inc. collaborates with healthcare professionals and institutions to drive clinical research and ensure the delivery of safe and effective medications to patients across the United States.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Chicago, Illinois, United States
Augusta, Georgia, United States
Winston Salem, North Carolina, United States
Dallas, Texas, United States
Cedarhurst, New York, United States
Glen Oaks, New York, United States
Garden Grove, California, United States
San Diego, California, United States
Salt Lake City, Utah, United States
Dallas, Texas, United States
Paramount, California, United States
Pasadena, California, United States
Atlanta, Georgia, United States
Dallas, Texas, United States
Lake Charles, Louisiana, United States
Denver, Colorado, United States
Escondido, California, United States
Little Rock, Arkansas, United States
Oakland, California, United States
Pico Rivera, California, United States
San Diego, California, United States
Torrance, California, United States
St. Charles, Missouri, United States
Durham, North Carolina, United States
Philadelphia, Pennsylvania, United States
Austin, Texas, United States
Dallas, Texas, United States
Houston, Texas, United States
Patients applied
Trial Officials
Lurasidone Medical Director, MD
Study Director
Sumitomo Pharma America, Inc.
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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