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Belhaven BioPharma Intranasal Epinephrine Patent Application

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Summary

Belhaven BioPharma Inc. filed US Patent Application US20260108687A1 on June 19, 2025, covering intranasal dry powder epinephrine compositions for treating anaphylaxis, bronchospasms, respiratory impairment, organophosphate poisoning, and major adverse cardiac events. The application was published April 23, 2026, naming inventors Scott Lyman and Brian Taubenheim. CPC classifications include A61M 15/08, A61K 9/0043, A61K 31/137, A61K 47/12, A61K 47/26, A61M 11/003, and A61M 11/007.

“The compositions include epinephrine or a pharmaceutically acceptable salt thereof, as well as a stabilizing agent and a carrier.”

USPTO , verbatim from source
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About this source

USPTO classification A61M covers devices that introduce or withdraw fluids from the body: infusion pumps, catheters, syringes, inhalers, wound drainage, dialysis equipment, and fluid-handling microfluidics. Every newly published application in A61M lands in this feed, around 205 a month. Applications publish 18 months after filing. Watch this if you compete in infusion therapy or drug delivery, file freedom-to-operate analyses for medical device startups, scout acquisition targets in cardiovascular or respiratory devices, or track hospital R&D arms that are quietly patenting clinical innovations.

What changed

Belhaven BioPharma Inc. filed US Patent Application US20260108687A1 covering intranasal dry powder epinephrine compositions including epinephrine or a pharmaceutically acceptable salt, a stabilizing agent (citric acid or salt), and a carrier. The compositions are intended for treating health conditions threatening the central nervous system and impeding alpha and beta-adrenergic receptor action, including anaphylaxis, bronchospasms, respiratory impairment, organophosphate poisoning, and MACE.

Pharmaceutical companies developing epinephrine delivery systems or competing products should review this application to assess freedom-to-operate implications. Medical device manufacturers in the nasal drug delivery space may need to evaluate potential overlap with the CPC classifications cited.

Archived snapshot

Apr 24, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← USPTO Patent Applications

COMPOSITIONS, DEVICES, AND METHODS FOR INTRANASAL DELIVERY OF DRY POWDER EPINEPHRINE

Application US20260108687A1 Kind: A1 Apr 23, 2026

Assignee

Belhaven BioPharma Inc.

Inventors

Scott Lyman, Brian Taubenheim

Abstract

Intranasal dry powder epinephrine compositions are described herein. The compositions include epinephrine or a pharmaceutically acceptable salt thereof, as well as a stabilizing agent and a carrier. The stabilizing agent is operable to include citric acid, or a pharmaceutically acceptable salt derived therefrom. Such intranasal compositions as described herein are useful in the treatment of health conditions which threaten the central nervous system (CNS) and impede the actions of alpha and beta-adrenergic receptors. Such health conditions include anaphylaxis, bronchospasms, respiratory impairment, organophosphate poisoning, and major adverse cardiac events (MACE).

CPC Classifications

A61M 15/08 A61K 9/0043 A61K 31/137 A61K 47/12 A61K 47/26 A61M 11/003 A61M 11/007

Filing Date

2025-06-19

Application No.

19243303

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Last updated

Classification

Agency
USPTO
Published
April 23rd, 2026
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
US20260108687A1

Who this affects

Applies to
Pharmaceutical companies Medical device makers
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Patent application Nasal drug delivery Epinephrine formulations
Geographic scope
United States US

Taxonomy

Primary area
Intellectual Property
Operational domain
Legal
Topics
Pharmaceuticals Medical Devices

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