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REGENXBIO presented interim clinical data for RGX-202, an investigational gene therapy designed to treat Duchenne Muscular Dystrophy, at the American Society of Gene & Cell Therapy conference in May 2024. The therapy features a novel microdystrophin transgene engineered to encode key functional domains of naturally occurring dystrophin to prevent muscle degeneration.
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16 Pages
Cytek Biosciences
Adani Transmission Limited 2022 Asian Credit Conference Presentation
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40 Pages
Adani Transmission Limited