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Data updated: Mar 10, 2026

LATUDA

LURASIDONE HYDROCHLORIDE
Neurology Approved 2010-10-28
5
Indications
--
Phase 3 Trials
1
Priority Reviews
15
Years on Market

Details

Status
Prescription
First Approved
2010-10-28
Routes
ORAL
Dosage Forms
TABLET

Companies

Active Ingredient: LURASIDONE HYDROCHLORIDE

LATUDA Approval History

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What LATUDA Treats

2 indications

LATUDA is approved for 2 conditions since its original approval in 2010. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Schizophrenia
  • Bipolar Disorder
Source: FDA Label

LATUDA Boxed Warning

INCREASED MORTALITY IN ELDERLY PATIENTS WITH DEMENTIA-RELATED PSYCHOSIS; and SUICIDAL THOUGHTS AND BEHAVIORS WARNING: INCREASED MORTALITY IN ELDERLY PATIENTS WITH DEMENTIA-RELATED PSYCHOSIS; and SUICIDAL THOUGHTS AND BEHAVIORS See full prescribing information for complete boxed warning. Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. LATUDA is not approved for the treatment of patients with dementia-related psychosis ( 5.1 ). A...

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

LATUDA FDA Label Details

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Indications & Usage

FDA Label (PDF)

LATUDA is indicated for: Treatment of adult and adolescent patients (13 to 17 years) with schizophrenia [see Clinical Studies ] . Monotherapy treatment of adult and pediatric patients (10 to 17 years) with major depressive episode associated with bipolar I disorder (bipolar depression) [see Clinical Studies ] . Adjunctive treatment with lithium or valproate in adult patients with major depressive episode associated with bipolar I disorder (bipolar depression) [see Clinical Studies ] . LATUDA is an atypical antipsychotic indicated for the treatment of: Schizophrenia in adults and adolescents (1...

โš ๏ธ BOXED WARNING

WARNING: INCREASED MORTALITY IN ELDERLY PATIENTS WITH DEMENTIA-RELATED PSYCHOSIS; and SUICIDAL THOUGHTS AND BEHAVIORS WARNING: INCREASED MORTALITY IN ELDERLY PATIENTS WITH DEMENTIA-RELATED PSYCHOSIS; and SUICIDAL THOUGHTS AND BEHAVIORS See full prescribing information for complete boxed warning. Eld...

LATUDA Patents & Exclusivity

Latest Patent: Nov 2031

Patents (275 active)

US9259423*PED Expires Nov 23, 2031
US9259423 Expires May 23, 2031
US9827242 Expires May 23, 2031
US8883794*PED Expires Nov 26, 2026
US8729085*PED Expires Nov 26, 2026
US9907794*PED Expires Nov 26, 2026
US9555027 Expires May 26, 2026
US8729085 Expires May 26, 2026
US9907794 Expires May 26, 2026
US8883794 Expires May 26, 2026
+ 265 more patents
Source: FDA Orange Book

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.