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MRG-110 is a locked nucleic acid-modified antisense oligonucleotide designed to inhibit microRNA-92a (miR-92a). By targeting and inhibiting miR-92a, which is known to negatively regulate angiogenesis and tissue repair, MRG-110 promotes the growth of new blood vessels (angiogenesis) and accelerates wound healing. Preclinical studies demonstrated that inhibition of miR-92a by MRG-110 increases vascularization and improves functional outcomes in models of heart failure and wound healing. In clinical trials, administration of MRG-110 led to increased perfusion and histological markers of neoangiogenesis as well as reduced expression of alpha-smooth muscle actin (α-SMA), correlating with decreased activation of myofibroblasts. The drug was developed for potential use in conditions where vascular flow is compromised such as heart failure, ischemia, and wounds[2][3][4][5][7].
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