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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

Lurasidone Schizophrenia Latuda

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.

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

0 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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