TheraRadar
Data updated: May 26, 2026

TRINTELLIX (vortioxetine hydrobromide)

Trial Activity: Declining 5 active trials
CNS Approved 2013-09-30

TRINTELLIX is indicated for the treatment of Major Depressive Disorder.

Source: FDA Label • Takeda

How TRINTELLIX Works

The exact mechanism of vortioxetine's antidepressant effect is not fully understood but is thought to be related to the enhancement of serotonergic activity in the CNS through the inhibition of serotonin reuptake. It also functions as a 5-HT3 receptor antagonist and a 5-HT1A receptor agonist; however, the specific contribution of these individual activities to the drug's efficacy has not been established.

Development Insights

Takeda conducting 22 trials (39%)
53 indications explored (Broad Platform)
major depressive disorder (17 trials)
depressive disorder, major (8 trials)
depression (6 trials)
7
Indications
--
Phase 3 Trials
2
Priority Reviews
12
Years on Market

Details

Status
Prescription
First Approved
2013-09-30
Patent Cliff
2032

Pro Metrics

Patent cliff and revenue data

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Routes
ORAL
Dosage Forms
TABLET

Companies

Active Ingredient: VORTIOXETINE HYDROBROMIDE

TRINTELLIX Approval History

2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
84 FDA actions from 2013 to 2023 · 6 indication expansions
Aug 2023 SUPPL Priority
Efficacy
Aug 2023 SUPPL
Label · Labeling
Sep 2021 SUPPL
Label · Labeling

What TRINTELLIX Treats

1 indications

TRINTELLIX is approved for 1 conditions since its original approval in 2013. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Major Depressive Disorder
Source: FDA Label

TRINTELLIX Boxed Warning

SUICIDAL THOUGHTS AND BEHAVIORS Antidepressants increased the risk of suicidal thoughts and behavior in pediatric and young adult patients in short-term studies. Closely monitor all antidepressant-treated patients for clinical worsening, and for emergence of suicidal thoughts and behaviors [see Warnings and Precautions (5.1) ] . TRINTELLIX is not approved for use in pediatric patients [see Use in Specific Populations (8.4) ] . WARNING: SUICIDAL THOUGHTS AND BEHAVIORS See full prescribing informa...

TRINTELLIX Competitive Set

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Three rings of competition based on shared molecular targets and treated indications.

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Filters applied: drops same-active-ingredient (505(b)(2) reformulations), route-mismatch (topical vs systemic), and cross-therapeutic-area matches in same-indication rings.

Drugs Similar to TRINTELLIX

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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.

TRINTELLIX FDA Label Details

Indications & Usage

FDA Label (PDF)

TRINTELLIX is indicated for the treatment of Major Depressive Disorder.

⚠️ BOXED WARNING

WARNING: SUICIDAL THOUGHTS AND BEHAVIORS Antidepressants increased the risk of suicidal thoughts and behavior in pediatric and young adult patients in short-term studies. Closely monitor all antidepressant-treated patients for clinical worsening, and for emergence of suicidal thoughts and behaviors ...

View full patent landscape →
20 OB patents · 3 families · 292 international docs across 45 countries

TRINTELLIX Patents & Exclusivity

Latest Patent: Sep 2032
Exclusivity: Feb 2027

Patents (20 active)

US9278096*PED Expires Sep 21, 2032
US9278096 Expires Mar 21, 2032
US8722684*PED Expires Dec 30, 2031
US8722684 Expires Jun 30, 2031
US8969355*PED Expires Dec 15, 2027
US9227946*PED Expires Dec 15, 2027
US9125908*PED Expires Dec 15, 2027
US9125909*PED Expires Dec 15, 2027
US9125910*PED Expires Dec 15, 2027
US9861630*PED Expires Dec 15, 2027
US11458134*PED Expires Dec 15, 2027
US9227946 Expires Jun 15, 2027
US9861630 Expires Jun 15, 2027
US9125908 Expires Jun 15, 2027
US9125909 Expires Jun 15, 2027
US9125910 Expires Jun 15, 2027
US8969355 Expires Jun 15, 2027
US11458134 Expires Jun 15, 2027
US7144884*PED Expires Dec 17, 2026
US7144884 Expires Jun 17, 2026

Exclusivity

M-232 Until Aug 2026
M-232 Until Aug 2026
M-232 Until Aug 2026
M-232 Until Aug 2026
PED Until Feb 2027
PED Until Feb 2027
PED Until Feb 2027
PED Until Feb 2027
M-232 Until Aug 2026
M-232 Until Aug 2026
M-232 Until Aug 2026
M-232 Until Aug 2026
PED Until Feb 2027
PED Until Feb 2027
PED Until Feb 2027
PED Until Feb 2027
M-232 Until Aug 2026
M-232 Until Aug 2026
M-232 Until Aug 2026
M-232 Until Aug 2026
PED Until Feb 2027
PED Until Feb 2027
PED Until Feb 2027
PED Until Feb 2027
M-232 Until Aug 2026
M-232 Until Aug 2026
M-232 Until Aug 2026
M-232 Until Aug 2026
PED Until Feb 2027
PED Until Feb 2027
PED Until Feb 2027
PED Until Feb 2027
Source: FDA Orange Book

Pro Intelligence Preview

Deep insights for TRINTELLIX

Revenue Insights

  • Quarterly revenue tracking
  • Historical trend analysis

Patent Timeline

  • Cliff: 2032
  • 320 active patents

Trial Analysis

  • 56 total trials
  • Stage: Declining

Competitive Landscape

  • 20 similar drugs
  • Same target/indication analysis
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Full approval history • All patents • Revenue trends • Competitor analysis

Data Sources

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

How We Calculate These Metrics

Trial Activity Stage

Measures the current development activity pattern based on trial phases, status, and trends. Important: This measures R&D activity, not commercial lifecycle.

Trial statuses: "Active" means recruiting or ongoing. "Completed" means reached planned endpoint. "Terminated" means stopped early—often due to safety, efficacy, or business reasons.

  • Growth: High proportion of early-phase trials (Phase 1/2), active development
  • Expansion: Significant Phase 3 activity, approaching or pursuing approvals
  • Mature: Substantial Phase 4 post-marketing studies
  • Stable: Mixed phase distribution, steady development
  • Declining: Low active trial ratio, reduced R&D investment