Clinical TrialsThe launch of the FLT3/NPM1 co-mutation arm in the KOMET-007 trial represents a significant advancement in treating AML patients with poor prognosis.
Regulatory ApprovalIn agreement with the FDA, each trial design includes dual-primary endpoints to support potential U.S. accelerated approval and full approval.
Safety ProfileThe new results continue to support ziftomenib’s favorable safety profile and encouraging efficacy in combination with SoC.
Therapeutic PotentialKura's commitment to exploring ziftomenib's efficacy in frontline AML settings highlights the company's dedication to improving treatment options.