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CUR102 is a discovery-stage microRNA (miRNA) therapeutic being developed by Curamys for the treatment of Duchenne Muscular Dystrophy (DMD). The drug candidate is designed to target specific disease-associated microRNAs that are implicated in the pathogenesis of DMD. By modulating the levels or activity of these miRNAs, CUR102 aims to regulate gene expression pathways involved in muscle degeneration and regeneration, potentially offering a novel approach to slowing disease progression in patients with DMD. As part of Curamys's broader miRNA platform, CUR102 represents a targeted approach to addressing the underlying molecular drivers of muscular dystrophy.
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