Lurasidone is an atypical antipsychotic developed by Dainippon Sumitomo Pharma. It was approved by the U.S. Food and Drug Administration (FDA) for treatment of schizophrenia on October 29, 2010 and is currently pending approval for the treatment of bipolar disorder in the United States.
Lurasidone is indicated for the treatment of schizophrenia in patients ≥13 years old. It is also indicated as a monotherapy for the treatment of bipolar depression in patients ≥10 years old, or in combination with lithium or valproate for the treatment of bipolar depression in adults.
Collaborative Neuroscience Network, South Bay, Torrance, California, United States
Comprehensive NeuroScience, Inc., Atlanta, Georgia, United States
CRI Worldwide - Kirkbride Center, Philadelphia, Pennsylvania, United States
Covance Global Clinical Research Unit Inc., Madison, Wisconsin, United States
PAREXEL Clinical Pharmacology Research Unit, Baltimore, Maryland, United States
CCT/Parexel, Culver City, California, United States
California Clinical Trials (CCT), Glendale, California, United States
California Clinical Trials, Culver City, California, United States
CCT/Parexel, Culver City, California, United States
Clinical Research Institute, Wichita, Kansas, United States
California Clinical Trials, Glendale, California, United States
CRI Worldwide, LLC, Philadelphia, Pennsylvania, United States
Mood Disorders Program-UHCMC, Cleveland, Ohio, United States
R.K. Yadav Memorial Mental Health & De-Addiction Hospital, Jaipur, Rajasthan, India
Clintrial, s.r.o., Praha, Czech Republic
Manobal Med. Research Centre, Lucknow, Uttar Prad, India
Spitalul Clinic Judetean de Urgenta Cluj, Cluj-Napoca, Romania
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