Changeflow GovPing Pharma & Drug Safety Enzyme-Cleavable Prodrug Compositions and Contr...
Routine Notice Added Final

Enzyme-Cleavable Prodrug Compositions and Controlled Release Nafamostat Methods

Favicon for changeflow.com USPTO Patent Grants - Pharma (A61K)
Published
Detected
Email

Summary

USPTO granted patent US12599578B2 to Ensysce Biosciences Inc. for pharmaceutical compositions including enzyme-cleavable prodrugs providing enzymatically-controlled release of active agents, combined with controlled release nafamostat. The patent covers 12 claims and methods of use for these pharmaceutical compositions.

Published by USPTO on changeflow.com . Detected, standardized, and enriched by GovPing. Review our methodology and editorial standards .

What changed

USPTO issued patent US12599578B2 to Ensysce Biosciences Inc. covering pharmaceutical compositions that combine enzyme-cleavable prodrugs with controlled release nafamostat. The invention provides for enzymatically-controlled release of active agents and applies to A61K pharmaceutical compositions.

For pharmaceutical companies and drug developers, this patent establishes IP protection for prodrug delivery technologies. The grant may affect freedom-to-operate analyses for competing formulations involving nafamostat or similar controlled release mechanisms.

Archived snapshot

Apr 17, 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 Grants

Compositions comprising enzyme-cleavable prodrugs and controlled release nafamostat and methods of use thereof

Grant US12599578B2 Kind: B2 Apr 14, 2026

Assignee

Ensysce Biosciences Inc.

Inventors

Lynn Kirkpatrick

Abstract

Aspects of the present disclosure include pharmaceutical compositions, and their methods of use, where the pharmaceutical compositions include an active agent prodrug that provides enzymatically-controlled release of an active agent, and controlled release nafamostat or a pharmaceutically acceptable salt thereof.

CPC Classifications

A61K 31/155 A61K 47/65 A61K 47/64 A61K 9/1623 A61K 9/1635 A61K 9/1652 A61K 38/07 A61K 47/32 A61K 47/38

Filing Date

2022-03-08

Application No.

17689271

Claims

12

View original document →

Get daily alerts for USPTO Patent Grants - Pharma (A61K)

Daily digest delivered to your inbox.

Free. Unsubscribe anytime.

About this page

What is GovPing?

Every important government, regulator, and court update from around the world. One place. Real-time. Free. Our mission

What's from the agency?

Source document text, dates, docket IDs, and authority are extracted directly from USPTO.

What's AI-generated?

The summary, classification, recommended actions, deadlines, and penalty information are AI-generated from the original text and may contain errors. Always verify against the source document.

Last updated

Classification

Agency
USPTO
Published
April 14th, 2026
Instrument
Notice
Legal weight
Binding
Stage
Final
Change scope
Minor
Document ID
US12599578B2

Who this affects

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

Taxonomy

Primary area
Intellectual Property
Operational domain
Legal
Topics
Pharmaceuticals Healthcare

Get alerts for this source

We'll email you when USPTO Patent Grants - Pharma (A61K) publishes new changes.

Free. Unsubscribe anytime.

You're subscribed!