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Revumenib is an oral, small molecule menin inhibitor used for the treatment of acute leukemias harboring lysine methyltransferase 2A gene (KMT2A, also known as MLL) rearrangements. It works by disrupting the interaction between menin and KMT2A, a protein complex that drives leukemogenesis in these cancers. By blocking this interaction, revumenib downregulates oncogenic gene expression and promotes differentiation or death of leukemia cells. The drug is indicated for relapsed or refractory acute leukemia with KMT2A translocation in adults and pediatric patients aged 1 year and older. Revumenib was developed by Syndax Pharmaceuticals and is marketed under the brand name Revuforj[1][4][5][6][7][8].
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