Commercial MomentumSyndax has entered a new phase of executional depth as Revuforj advances from its initial launch in relapsed or refractory leukemia toward first-line expansion, with commercial traction already exceeding expectations through rapid formulary access and sustained treatment persistence.
FDA ApprovalRevuforj received FDA approval for the treatment of relapsed or refractory NPM1-mutated AML, expanding its reach into the largest molecularly defined AML subgroup.
Market OpportunityRevumenib now addresses more than 6,500 U.S. relapsed or refractory acute leukemia patients annually, creating a greater than $2B market opportunity.