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.
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Syndax presented data from the pivotal Phase II AUGMENT-101 trial of revumenib in KMT2Ar acute myeloid leukemia and acute lymphoid leukemia at the ASH late-breaking abstract session.
The company presented results from the pivotal Phase II AUGMENT-101 trial in a late-breaking abstract at the American Society of...







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