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Intranasal Dry Powder Epinephrine Patent Application, Belhaven BioPharma

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Summary

Belhaven BioPharma Inc. filed US Patent Application US20260108686A1 on June 18, 2025, covering intranasal dry powder epinephrine compositions for treating anaphylaxis, bronchospasms, respiratory impairment, organophosphate poisoning, and major adverse cardiac events. The application claims compositions including epinephrine with citric acid or a salt as a stabilizing agent and a carrier, classified under CPC codes A61M 15/08 and A61K 9/0043. Inventors Scott Lyman and Brian Taubenheim are named on the application.

“Intranasal dry powder epinephrine compositions are described herein.”

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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 a patent application with the USPTO for intranasal dry powder epinephrine compositions. The compositions include epinephrine or a pharmaceutically acceptable salt, a stabilizing agent (citric acid or derivative), and a carrier. The application covers methods for treating conditions affecting the central nervous system including anaphylaxis, bronchospasms, respiratory impairment, organophosphate poisoning, and major adverse cardiac events.

Pharmaceutical manufacturers and drug delivery developers should monitor this filing as it may indicate competitive landscape considerations for epinephrine delivery alternatives. Patent applicants may reference this application during prior art searches for dry powder or intranasal epinephrine technologies.

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 US20260108686A1 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 imped 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

2025-06-18

Application No.

19242195

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Last updated

Classification

Agency
USPTO
Published
June 18th, 2025
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Draft
Change scope
Minor
Document ID
US20260108686A1

Who this affects

Applies to
Pharmaceutical companies
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Patent application Pharmaceutical development
Geographic scope
United States US

Taxonomy

Primary area
Intellectual Property
Operational domain
Legal
Topics
Healthcare Medical Devices

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