Efficacy And SafetyThe BEAT study demonstrates strong performance with a 100% overall response rate and a 95% complete remission rate, indicating high efficacy of the treatment.
Market PositionSyndax is already first to market in r/r KMT2Ar acute leukemias and will likely be first to market in NPM1m, historically providing an advantage in market share.
Regulatory ApprovalRevuforj received FDA approval for the treatment of adult and pediatric patients one year and older with r/r acute leukemia with a KMT2A translocation.