Dyne Therapeutics‘s patent involves complexes with muscle-targeting agents linked to molecular payloads, inhibiting DUX4 expression. Claim 1 specifies an anti-transferrin receptor antibody linked to an oligonucleotide targeting a specific region of human transferrin receptor protein 1. The oligonucleotide includes modifications and a region complementary to a specific nucleotide sequence. GlobalData’s report on Dyne Therapeutics gives a 360-degree view of the company including its patenting strategy. Buy the report here.
According to GlobalData’s company profile on Dyne Therapeutics, Antibody-conjugate nanoparticles was a key innovation area identified from patents. Dyne Therapeutics's grant share as of May 2024 was 2%. Grant share is based on the ratio of number of grants to total number of patents.
Complex of anti-transferrin receptor antibody linked to oligonucleotide
A recently granted patent (Publication Number: US12012460B2) discloses a complex comprising an anti-transferrin receptor antibody covalently linked to an oligonucleotide. The antibody binds to a specific region of the human transferrin receptor protein 1 (TfR1) and the oligonucleotide contains modifications and a region of complementarity to a specific nucleotide sequence. The modifications include 2'-modified nucleosides and a modified backbone, and the oligonucleotide ranges from 15-30 nucleotides in length. Additionally, the complex can be obtained through a cycloaddition reaction involving specific linkers and sugar molecules can be part of the antibody structure.
Furthermore, the patent claims cover variations in the length of the region of complementarity, the type of oligonucleotide used (such as phosphorodiamidate morpholino oligomer), and the specific antibodies involved (such as ScFv, Fab fragment). The complex is designed for targeting genes associated with diseases related to muscle weakness, including muscular dystrophy, by binding to specific regions of the transferrin receptor protein. The patent also details the use of cleavable linkers and specific sequences for the covalent linkage between the antibody and the oligonucleotide, providing a novel approach for therapeutic interventions targeting muscle-related disorders.
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