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ActRIIB Variants Treat Neuromuscular, Osteogenesis Imperfecta

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Summary

The USPTO published patent application US20260108585A1 on April 23, 2026, covering pharmaceutical compositions of extracellular ActRIIB variant polypeptides fused to Fc domains for treating multiple conditions including neuromuscular diseases, osteogenesis imperfecta, myelofibrosis, thrombocytopenia, neutropenia, and metabolic disease. The application, filed September 17, 2025, under application number 19331002, names Jasbir S. Seehra, Jennifer Lachey, and Elissa Furutani as inventors. CPC classifications include A61K 38/179, A61K 35/19, and C07K 14/78.

“The invention features polypeptides that include an extracellular ActRIIB variant.”

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

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

The USPTO published patent application US20260108585A1 disclosing compositions and methods of use for extracellular ActRIIB variant polypeptides, optionally fused to an Fc domain monomer or moiety, for therapeutic applications. The filing covers treatment of neuromuscular diseases, osteogenesis imperfecta, myelofibrosis, thrombocytopenia, neutropenia, and metabolic disease. The application was filed on September 17, 2025, under application number 19331002.

Pharmaceutical companies and researchers developing ActRIIB-related therapeutics should review this published application to assess potential freedom-to-operate considerations and competitive patent landscape. The published CPC codes A61K and C07K indicate the application's relevance to pharmaceutical composition and protein therapeutic development programs.

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

METHODS OF USING ACTIVIN RECEPTOR TYPE IIB VARIANTS

Application US20260108585A1 Kind: A1 Apr 23, 2026

Inventors

Jasbir S. SEEHRA, Jennifer LACHEY, Elissa FURUTANI

Abstract

The invention features polypeptides that include an extracellular ActRIIB variant. In some embodiments, a polypeptide of the invention includes an extracellular ActRIIB variant fused to an Fc domain monomer or moiety. The invention also features pharmaceutical compositions containing said polypeptides and methods of using the polypeptides to treat diseases and conditions including neuromuscular diseases, osteogenesis imperfecta, myelofibrosis, thrombocytopenia, neutropenia, and metabolic disease.

CPC Classifications

A61K 38/179 A61K 35/19 C07K 14/78 C07K 2319/30

Filing Date

2025-09-17

Application No.

19331002

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Last updated

Classification

Agency
USPTO
Published
April 23rd, 2026
Instrument
Rule
Branch
Executive
Legal weight
Binding
Stage
Final
Change scope
Minor
Document ID
US20260108585A1

Who this affects

Applies to
Pharmaceutical companies Manufacturers
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Patent application Therapeutic composition research
Geographic scope
United States US

Taxonomy

Primary area
Intellectual Property
Operational domain
Regulatory Affairs
Topics
Pharmaceuticals Healthcare

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