Syndax Pharmaceuticals, Inc. is starting out with a rare subset of acute leukemia patients when it submits revumenib for US Food and Drug Administration review at the end of the year, but it is also aiming for a larger subset that could potentially yield a blockbuster opportunity, one in which others hope to compete as well.
Syndax’s Revumenib Makes Splash At ASH As Company Eyes Blockbuster Opportunity
The company presented data for the menin inhibitor in KMT2Ar acute leukemias in an ASH late-breaker. The larger addressable population, including mNPM1 AML, could be a $2bn opportunity.

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Pipeline Watch is a weekly snapshot of selected late-stage clinical trial events and approvals announced by pharmaceutical and biotech companies at medical and industry conferences, in financial and company presentations, and in company releases and statements.
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