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Patent Application for Tenosynovial Giant Cell Tumor Treatment

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Summary

The USPTO has published a patent application (US20260085124A1) detailing compositions and methods for treating tenosynovial giant cell tumor using intra-articular delivery of anti-CSF1R antibodies. The application, filed by Kirk William Johnson, focuses on sustained drug exposure within joints.

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

What changed

This document is a patent application (US20260085124A1) filed with the USPTO, detailing novel methods for treating tenosynovial giant cell tumor. The application describes compositions and techniques for intra-articular delivery of anti-CSF1R antibodies, aiming for sustained therapeutic activity within joints beyond conventional short dwell times.

As this is a patent application, it does not impose immediate regulatory obligations or deadlines on regulated entities. However, it signifies potential future developments in pharmaceutical treatments for specific joint diseases. Companies involved in drug development, particularly in oncology and rheumatology, may find this application relevant for competitive intelligence and potential licensing opportunities.

Archived snapshot

Mar 26, 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

TREATMENT OF TENOSYNOVIAL GIANT CELL TUMOR

Application US20260085124A1 Kind: A1 Mar 26, 2026

Inventors

Kirk William Johnson

Abstract

The present disclosure provides compositions and methods for intra-articular delivery of anti-CSF1R antibodies to a joint that is impacted by a disease that is treatable with CSF1/CSF1R inhibition and/or that expresses CSF1R. It was conventional knowledge that the intra-articular dwell time of proteins in joints is typically a few hours or less. The present disclosure shows, however, that intra-articular delivery of an anti-CSF1R antibody can lead to sustained exposure and pharmacologic activity of the antibody in the joints far beyond a few hours, providing an effective means for targeted and extended delivery of the therapeutic agent.

CPC Classifications

C07K 16/2866 A61P 35/00 A61K 2039/505 A61K 2039/54 A61K 2039/545

Filing Date

2023-09-11

Application No.

19111100

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Named provisions

TREATMENT OF TENOSYNOVIAL GIANT CELL TUMOR

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Last updated

Classification

Agency
USPTO
Instrument
Notice
Legal weight
Non-binding
Stage
Draft
Change scope
Minor
Document ID
US20260085124A1

Who this affects

Applies to
Drug manufacturers Healthcare providers Patients
Industry sector
3254 Pharmaceutical Manufacturing 6211 Healthcare Providers
Activity scope
Drug Labeling Clinical Trial Reporting
Geographic scope
United States US

Taxonomy

Primary area
Pharmaceuticals
Operational domain
Legal
Compliance frameworks
FDA 21 CFR Part 11 GxP
Topics
Medical Devices Healthcare

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