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Mammoth Biosciences CRISPR Dystrophin Editing Patent Application

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Summary

USPTO published patent application US20260097134A1 assigned to Mammoth Biosciences, Inc. covering CRISPR-Cas systems and methods for editing human dystrophin genes to treat Duchenne muscular dystrophy (DMD). The application includes compact Type V CRISPR-associated proteins, RNA-dependent DNA polymerase, and guide nucleic acids for gene modification therapies.

What changed

USPTO published patent application US20260097134A1 from Mammoth Biosciences covering systems, compositions, and methods for modifying the human dystrophin gene using CRISPR-Cas technology for Duchenne muscular dystrophy treatment. The application includes compact Type V CRISPR-associated proteins, RNA-dependent DNA polymerase, and guide nucleic acids.

This patent application represents potential intellectual property protection for gene editing approaches targeting DMD. Parties conducting gene editing research or developing DMD treatments should monitor this application for potential freedom-to-operate implications.

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Archived snapshot

Apr 11, 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

COMPOSITIONS AND METHODS FOR PRECISE EDITING OF HUMAN DYSTROPHIN

Application US20260097134A1 Kind: A1 Apr 09, 2026

Assignee

Mammoth Biosciences, Inc.

Inventors

Yuchen GAO, Ning CHAI, Wiputra Jaya HARTONO, Benjamin Julius RAUCH, Aaron DELOUGHERY, Stepan TYMOSHENKO, William Douglass WRIGHT, Paula GONCALVES CERQUEIRA, Brian R. CHAIKIND, Kevin Cristopher WILKINS

Abstract

Disclosed herein are systems, compositions, and methods for modifying the human dystrophin gene (DMD). Systems, compositions, and methods may comprise a compact Type V CRISPR-associated (Cas) protein, an RNA-dependent DNA polymerase, and/or one or more guide nucleic acids or uses thereof. These systems, compositions, and methods may be useful for treating diseases such as Duchenne muscular dystrophy (DMD).

CPC Classifications

A61K 48/0058 C12N 9/1276 C12N 9/224 C12N 15/11 C12N 15/86 C12N 15/907 C12Y 207/07049 C12N 2310/20 C12N 2750/14143

Filing Date

2025-12-05

Application No.

19410151

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Last updated

Classification

Agency
USPTO
Published
April 9th, 2026
Instrument
Rule
Legal weight
Binding
Stage
Final
Change scope
Minor
Document ID
US20260097134A1
Docket
19410151

Who this affects

Applies to
Pharmaceutical companies Biotechnology companies
Industry sector
3254.1 Biotechnology
Activity scope
Patent application Gene therapy development
Geographic scope
United States US

Taxonomy

Primary area
Intellectual Property
Operational domain
Legal
Topics
Pharmaceuticals Healthcare

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