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Dystrophin messenger ribonucleic acid (mRNA) is a preclinical therapeutic candidate being developed by Factor Biosciences Therapeutics for the treatment of Duchenne Muscular Dystrophy (DMD). This program utilizes mRNA-mediated in vivo gene editing to target and potentially correct mutations in the dystrophin gene, or to facilitate the expression of a functional dystrophin protein. By leveraging Factor's proprietary mRNA and nucleic-acid delivery technologies, the therapy aims to restore dystrophin levels in muscle tissues, addressing the underlying cause of muscle degeneration. The asset is currently in the preclinical stage of development as part of Factor's internal pipeline.
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