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Dual-Chamber Drug Delivery Patent, Semaglutide and Cagrilintide

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Summary

USPTO Application US20260108587A1, published April 23, 2026, covers aqueous pharmaceutical formulations of semaglutide and cagrilintide designed for co-administration via a dual-chamber medical device. The inventors are Tommy Sander, Christian Poulsen, and Rosa Rebecca Erritzoee Hansen. Filing date was December 17, 2025, under Application No. 19423120. CPC classifications include A61K 38/26 (GLP-1 peptides), A61M 5/19 (infusion devices), and various formulation excipients.

“Disclosed herein are an aqueous pharmaceutical formulation comprising cagrilintide and an aqueous formulation comprising semaglutide.”

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

USPTO published patent application US20260108587A1 for an aqueous pharmaceutical formulation comprising cagrilintide and a separate aqueous formulation comprising semaglutide, both designed for presentation and administration using a dual-chamber medical device.

Pharmaceutical companies developing GLP-1 combination therapies should review this filing for potential freedom-to-operate implications, as the dual-chamber device design and specific formulation combinations may represent competitive IP landscape considerations.

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

PHARMACEUTICAL FORMULATIONS

Application US20260108587A1 Kind: A1 Apr 23, 2026

Inventors

Tommy Sander, Christian Poulsen, Rosa Rebecca Erritzoee Hansen

Abstract

Disclosed herein are an aqueous pharmaceutical formulation comprising cagrilintide and an aqueous formulation comprising semaglutide. The compositions of these two pharmaceutical formulations allow for their presentation in, and administration using, the dual-chamber medical device disclosed herein. Individuals with diseases, such as diabetes and/or obesity and/or related co-morbidities, may benefit from the co-administration of semaglutide and cagrilintide, and/or of the two liquid pharmaceutical formulations disclosed herein, using the medical device disclosed herein.

CPC Classifications

A61K 38/26 A61K 9/0019 A61K 9/08 A61K 31/4172 A61K 38/1703 A61K 47/02 A61K 47/10 A61K 47/12 A61K 47/183 A61K 47/22 A61K 47/24 A61K 47/26 A61M 5/19

Filing Date

2025-12-17

Application No.

19423120

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Last updated

Classification

Agency
USPTO
Instrument
Rule
Branch
Executive
Legal weight
Binding
Stage
Draft
Change scope
Minor
Document ID
US20260108587A1

Who this affects

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

Taxonomy

Primary area
Intellectual Property
Operational domain
Legal
Topics
Pharmaceuticals Healthcare

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