Market OpportunityRevumenib now addresses more than 6,500 U.S. relapsed or refractory acute leukemia patients annually, creating a greater than $2B market opportunity.
Market PositionSyndax's earlier market entry, more mature safety dataset, and ongoing integration into transplant and maintenance settings collectively strengthen its position as the anchored menin inhibitor entrant in AML.
Regulatory ApprovalsRevuforj received FDA approval for the treatment of relapsed or refractory NPM1-mutated AML, expanding its reach into the largest molecularly defined AML subgroup.