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CUR101 is a preclinical-stage microRNA (miRNA) therapeutic candidate being developed by Curamys for the treatment of Duchenne Muscular Dystrophy (DMD). The drug is designed to target specific disease-associated microRNAs that are implicated in the pathogenesis and progression of DMD. By modulating the levels of these miRNAs, CUR101 aims to regulate gene expression pathways involved in muscle degeneration, inflammation, and fibrosis, potentially slowing or halting the progression of the disease. The program is part of Curamys's broader pipeline utilizing miRNA-based modalities to address neuromuscular and neurodegenerative conditions.
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