TheraRadar
Data updated: May 26, 2026

BREKIYA (AUTOINJECTOR) (dihydroergotamine mesylate)

CNS Approved 2025-05-14

Brekiya (dihydroergotamine mesylate) is an autoinjector indicated for the acute treatment of migraine headaches, with or without aura, and the acute treatment of cluster headache episodes in adults. It is intended for the immediate management of headache pain and is not indicated for the prophylactic therapy of migraine or cluster headaches.

Source: FDA Label • AMNEAL

How BREKIYA (AUTOINJECTOR) Works

Dihydroergotamine binds with high affinity to 5-HT1B, 5-HT1D, and 5-HT1F receptors. Its therapeutic efficacy in migraine is attributed to agonist activity at 5-HT1B and 5-HT1D receptors, which results in the constriction of inflamed intracranial blood vessels and the inhibition of pro-inflammatory neuropeptide release from trigeminal nerve endings. Dihydroergotamine also exhibits affinity for alpha-adrenergic and dopaminergic receptors.

1
Indication
--
Phase 3 Trials
1
Years on Market

Details

Status
Prescription
First Approved
2025-05-14
Patent Cliff
2039

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Routes
SUBCUTANEOUS
Dosage Forms
SOLUTION

Companies

Active Ingredient: DIHYDROERGOTAMINE MESYLATE

BREKIYA (AUTOINJECTOR) Approval History

2026
Original
New Indication
New Form
Label Update
1 FDA actions from 2025 to 2025
May 2025 ORIGINAL
Update · Type 5 - New Formulation or New Manufacturer

What BREKIYA (AUTOINJECTOR) Treats

2 indications

BREKIYA (AUTOINJECTOR) is approved for 2 conditions since its original approval in 2025. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Migraine
  • Cluster Headache
Source: FDA Label

BREKIYA (AUTOINJECTOR) Boxed Warning

PERIPHERAL ISCHEMIA FOLLOWING COADMINISTRATION WITH POTENT CYP3A4 INHIBITORS Serious and/or life-threatening peripheral ischemia has been associated with the co-administration of dihydroergotamine with potent CYP3A4 inhibitors including protease inhibitors and macrolide antibiotics. Because CYP3A4 inhibition elevates the serum levels of dihydroergotamine, the risk for vasospasm leading to cerebral ischemia and/or ischemia of the extremities is increased. Hence, concomitant use of these medicatio...

BREKIYA (AUTOINJECTOR) Competitive Set

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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 BREKIYA (AUTOINJECTOR)

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Trial Timeline

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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.

BREKIYA (AUTOINJECTOR) FDA Label Details

Indications & Usage

FDA Label (PDF)

BREKIYA (AUTOINJECTOR) is indicated for the treatment of Migraine; Cluster Headache.

⚠️ BOXED WARNING

WARNING: PERIPHERAL ISCHEMIA FOLLOWING COADMINISTRATION WITH POTENT CYP3A4 INHIBITORS Serious and/or life-threatening peripheral ischemia has been associated with the co-administration of dihydroergotamine with potent CYP3A4 inhibitors including protease inhibitors and macrolide antibiotics. Because...

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3 OB patents · 1 families · 10 international docs across 3 countries

BREKIYA (AUTOINJECTOR) Patents & Exclusivity

Latest Patent: Feb 2039

Patents (4 active)

US11819501 Expires Feb 26, 2039
US10532049 Expires Feb 26, 2039
US12533351 Expires Feb 26, 2039
US11304942 Expires Feb 26, 2039
Source: FDA Orange Book

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Patent Timeline

  • Cliff: 2039
  • 5 active patents

Trial Analysis

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  • Development stage analysis

Competitive Landscape

  • 20 similar drugs
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Data Sources

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