Avidity Set To File First Of Three Muscular Dystrophy Drugs In 2025

The company is moving quickly to bring its antibody oligonucleotide conjugates to patients in three separate muscular dystrophy diseases, causing unease for its rivals.

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Avidity Biosciences could be about to transform treatment of three muscular dystrophy diseases with first-in-class RNA-based therapies, the most advanced being on track for filing by the end of 2025.

The San Diego, CA-based firm is developing a new hybrid drug class called antibody oligonucleotide conjugates (AOCs), which use monoclonal antibodies to transport oligonucleotide therapies into muscle and cardiac tissue,

Early readouts from its candidates last year made the company one of best-performing mid-cap biopharma stocks in 2024, and

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