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Auto-Tuning Drug Regulator Construct, US20260108617A1

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Summary

USPTO published patent application US20260108617A1 for an auto-tuning drug regulator construct with a filing date of January 17, 2024. The invention describes a chemical construct comprising a biorecognition component, an incapacitation component, and an active drug component, where drug release is triggered by the presence or absence of a target enzyme. Six inventors are named: Tapash Jay Sarkar, Edward Njoo, Lorelei Xia, Akira Yamamoto, Zachary Bashkin, and Warren Chang. This document is a publication announcement only and creates no compliance obligations.

“The construct is a chemical structure comprising: (a) a biorecognition component comprising a substrate recognized by an enzyme, (b) an incapacitation component, and (c) an active drug component.”

USPTO , verbatim from source
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About this source

USPTO classification A61K covers pharmaceutical preparations: formulations, dosage forms, combination therapies, delivery systems, and the vehicles that carry active ingredients. Every newly published application in A61K lands in this feed, around 245 a month. Applications publish 18 months after filing, so this feed reveals what pharma formulators at major sponsors and generics were working on in the prior year and a half. Watch this if you compete in drug formulation, file freedom-to-operate analyses, scout competitive drug products before clinical readouts, or follow novel delivery platforms like nanoparticles, lipid carriers, and long-acting injectables.

What changed

USPTO published patent application US20260108617A1 for an auto-tuning drug regulator construct, classified under CPC A61K 47/65. The application claims a chemical structure with three integrated components: a biorecognition component recognized by a target enzyme, an incapacitation component that renders the drug benign upon substrate-enzyme interaction, and an active drug component that takes effect when the enzyme is inactive or absent.

Pharmaceutical and biotechnology companies developing enzyme-responsive drug delivery systems should note this filing as it may represent prior art for similar approaches. Patent applicants in this space should conduct clearance searches against the claims. No regulatory obligations or compliance deadlines arise from this publication.

Archived snapshot

Apr 23, 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

AUTO-TUNING DRUG REGULATOR CONSTRUCTIONS

Application US20260108617A1 Kind: A1 Apr 23, 2026

Inventors

Tapash Jay SARKAR, Edward NJOO, Lorelei XIA, Akira YAMAMOTO, Zachary BASHKIN, Warren CHANG

Abstract

The present invention provides a regulator construct in which the drug efficacy is auto-regulated by the presence of a indicator enzyme. The construct is a chemical structure comprising: (a) a biorecognition component comprising a substrate recognized by an enzyme, (b) an incapacitation component, and (c) an active drug component. The incapacitation component provides a chemical incapacitation mechanism to render benign or incapacitate the drug component, after the substrate-enzyme interaction, allowing additionally for the creation of altered benign chemical structures while, otherwise, when said enzymes is inactive or absent the drug will take effect.

CPC Classifications

A61K 47/65

Filing Date

2024-01-17

Application No.

19148655

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Last updated

Classification

Agency
USPTO
Published
April 23rd, 2026
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor

Who this affects

Applies to
Pharmaceutical companies
Industry sector
5411 Legal Services
Activity scope
Patent application Drug delivery system Biorecognition technology
Geographic scope
United States US

Taxonomy

Primary area
Intellectual Property
Operational domain
Legal
Topics
Pharmaceuticals

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