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.
The Brigham and Women's Hospital, Department of Psychiatry, Boston, Massachusetts, United States
University Hospitals Cleveland Medical Center, Cleveland, Ohio, United States
UBC Mood Disorders Center, Vancouver, British Columbia, Canada
New York State Psychiatric Institute, New York, New York, United States
UT Southwestern Medical Center, Dallas, Texas, United States
Xuhui Center Hospital, Shanghai, Shanghai, China
Xuhui Center Hospital, Shanghai, Shanghai, China
University of British Columbia, Department of Psychiatry, Vancouver, British Columbia, Canada
Psychiatric Associates, Overland Park, Kansas, United States
University Hospitals Case Medical Center, Cleveland, Ohio, United States
Harmonex Neuroscience Research, Dothan, Alabama, United States
Guangzhou Brain Hospital, Guangzhou, Guangdong, China
HeBei Mental Health Center, Baoding, Hebei, China
Tianjin Anding Hospital, Tianjin, Tianjin, China
Japan 76 sites, Tokyo, Japan
Lithuania 3 sites, Kaunas, Lithuania
Malaysia 5 sites, Kuala Lumpur, Malaysia
Ukraine 9 sites, Kiev, Ukraine
Slovakia 5 sites, Zilina, Slovakia
Malaysia 5 sites, Kuala Lumpur, Malaysia
Stay informed with timely notifications on clinical trials, regulatory changes, and research advancements related to this medication.