Lurasidone

Generic Name
Lurasidone
Brand Names
Latuda
Drug Type
Small Molecule
Chemical Formula
C28H36N4O2S
CAS Number
367514-87-2
Unique Ingredient Identifier
22IC88528T
Background

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.

Indication

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.

Associated Conditions
Depression, Bipolar, Schizophrenia
Associated Therapies
-

A Study to Test the Effectiveness and Safety of a New Medication in the Treatment of Schizophrenia

Phase 2
Completed
Conditions
Interventions
First Posted Date
2004-08-02
Last Posted Date
2016-04-08
Lead Sponsor
Sumitomo Pharma America, Inc.
Target Recruit Count
180
Registration Number
NCT00088634
Locations
🇺🇸

Birmingham Psychiatry Pharmaceutical, Birmingham, Alabama, United States

🇺🇸

Summit Research Group, Little Rock, Arkansas, United States

🇺🇸

Comprehensive NeuroScience, Cerritos, California, United States

and more 19 locations
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