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Belhaven BioPharma Intranasal Dry Powder Epinephrine Patent Application

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Summary

Belhaven BioPharma Inc. filed patent application US20260108688A1 for intranasal dry powder epinephrine compositions including a stabilizing agent (citric acid or salt) and carrier, dated October 29, 2025. The application covers methods for treating health conditions threatening the central nervous system including anaphylaxis, bronchospasms, respiratory impairment, organophosphate poisoning, and major adverse cardiac events. Inventors are Scott Lyman and Brian Taubenheim.

“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 patent application US20260108688A1 with the USPTO on October 29, 2025, covering intranasal dry powder epinephrine compositions combined with citric acid or a salt as a stabilizing agent and a carrier. The application identifies specific therapeutic uses including anaphylaxis, bronchospasms, respiratory impairment, organophosphate poisoning, and major adverse cardiac events.

Pharmaceutical and medical device companies developing epinephrine delivery systems should review this application to assess potential patent landscape implications for intranasal dry powder formulations. Competitors in the anaphylaxis treatment space may need to design around these claims or evaluate licensing opportunities with Belhaven BioPharma.

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 US20260108688A1 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

2025-10-29

Application No.

19372926

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Last updated

Classification

Agency
USPTO
Published
October 29th, 2025
Instrument
Rule
Branch
Executive
Legal weight
Binding
Stage
Final
Change scope
Minor
Document ID
US20260108688A1

Who this affects

Applies to
Pharmaceutical companies Drug manufacturers
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Patent filing Drug formulation Intranasal delivery
Geographic scope
United States US

Taxonomy

Primary area
Intellectual Property
Operational domain
Legal
Topics
Medical Devices Pharmaceuticals

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