TheraRadar

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Data updated: Mar 10, 2026

REXULTI

BREXPIPRAZOLE
Neurology Approved 2015-07-10
6
Indications
--
Phase 3 Trials
3
Priority Reviews
10
Years on Market

Details

Status
Prescription
First Approved
2015-07-10
Routes
ORAL
Dosage Forms
TABLET

Companies

Active Ingredient: BREXPIPRAZOLE

REXULTI Approval History

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What REXULTI Treats

3 indications

REXULTI is approved for 3 conditions since its original approval in 2015. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Major Depressive Disorder
  • Schizophrenia
  • Agitation associated with Dementia due to Alzheimer's Disease
Source: FDA Label

REXULTI 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 increased risk of death. REXULTI is not approved for the treatment of patients with dementia-related psychosis without agitat...

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Active Pipeline

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Ongoing clinical trials by development phase

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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.

REXULTI FDA Label Details

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Indications & Usage

FDA Label (PDF)

REXULTI is indicated for: Adjunctive treatment to antidepressants for major depressive disorder (MDD) in adults Treatment of schizophrenia in adults and pediatric patients ages 13 years and older Treatment of agitation associated with dementia due to Alzheimer's disease Limitations of Use: REXULTI is not indicated as an as needed ("prn") treatment for agitation associated with dementia due to Alzheimer's disease [see Clinical Studies ] . REXULTI is an atypical antipsychotic indicated for: Use as an adjunctive therapy to antidepressants for the treatment of major depressive disorder (MDD) in ad...

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. Elder...

REXULTI Patents & Exclusivity

Latest Patent: Apr 2033
Exclusivity: May 2028

Patents (492 active)

US10307419*PED Expires Apr 12, 2033
US10307419 Expires Oct 12, 2032
USRE48059*PED Expires Jun 23, 2029
USRE48059 Expires Dec 23, 2028
US9839637*PED Expires Oct 12, 2026
US8618109*PED Expires Oct 12, 2026
US7888362*PED Expires Oct 12, 2026
US8349840*PED Expires Oct 12, 2026
US8618109 Expires Apr 12, 2026
US8349840 Expires Apr 12, 2026
+ 482 more patents

Exclusivity

I-913 Until May 2026
M-14 Until May 2027
M-315 Until May 2028
I-913 Until May 2026
M-14 Until May 2027
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.