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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

A Comparison of Study Drug With Placebo and Haloperidol in Patients With Schizophrenia

Phase 2
Completed
Conditions
Schizophrenia
Interventions
First Posted Date
2002-08-20
Last Posted Date
2014-04-17
Lead Sponsor
Sumitomo Pharma America, Inc.
Target Recruit Count
356
Registration Number
NCT00044044
Locations
🇺🇸

Alexian Brothers Behavioral Health Hospital, Hoffman Estates, Illinois, United States

🇺🇸

ClinSearch, Inc., Kenilworth, New Jersey, United States

🇺🇸

Claghorn Lesem Research Clinic, Inc., Bellaire, Texas, United States

and more 30 locations
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