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Large-Scale Liposomal Aminoglycoside Manufacturing Method

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Summary

USPTO published patent application US20260096989A1 by Insmed Incorporated for large-scale manufacturing of liposomal aminoglycoside drug formulations. The method uses a specific lipid-to-drug stream flow rate ratio to achieve high encapsulation efficiency with a lipid-to-drug weight ratio below 1:1.

What changed

USPTO published Insmed's patent application for a large-scale manufacturing method of liposomal drug formulations containing aminoglycosides such as amikacin. The method utilizes a specific relative flow rate ratio of lipid to drug streams to produce liposomes with high encapsulation efficiency, resulting in formulations with an overall lipid-to-drug weight ratio of less than 1:1. The patent is classified under CPC codes A61K 9/1277 (liposomes) and A61K 31/7036 (amikacin derivatives).

For pharmaceutical manufacturers developing or producing liposomal aminoglycoside formulations, this patent establishes intellectual property protection for Insmed's manufacturing process. Competitors seeking to manufacture similar formulations at scale may need to design around these claims or seek licensing arrangements. The application was filed December 9, 2025, under application number 19413999.

What to do next

  1. Monitor for patent grant and assess freedom-to-operate implications for competing liposomal aminoglycoside products
  2. Review patent claims for potential licensing opportunities if manufacturing similar formulations

Archived snapshot

Apr 10, 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

LARGE-SCALE MANUFACTURING METHODS FOR AMINOGLYCOSIDES

Application US20260096989A1 Kind: A1 Apr 09, 2026

Assignee

Insmed Incorporated

Inventors

Robert WORSHAM

Abstract

Provided herein is a method for the large-scale manufacture of liposomal drug formulations containing an aminoglycoside such as amikacin having advantageous lipid/drag characteristics. The method utilizes a particular relative flow rate ratio of lipid to drug streams to obtain liposomes with a high aminoglycoside encapsulation efficiency. The resulting liposomal drug formulations advantageously comprise an overall lipid-to-drug weight ratio of less than 1:1.

CPC Classifications

A61K 9/1277 A61K 31/7036

Filing Date

2025-12-09

Application No.

19413999

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Last updated

Classification

Agency
USPTO
Published
April 9th, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
US20260096989A1

Who this affects

Applies to
Pharmaceutical companies Drug manufacturers Manufacturers
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Pharmaceutical manufacturing Drug formulation development Lipid-based drug delivery
Geographic scope
United States US

Taxonomy

Primary area
Intellectual Property
Operational domain
Legal
Topics
Pharmaceuticals Healthcare

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