Syndax says revumenib plus intensive chemo posts 97% remission rate in Phase 1 newly diagnosed AML trial at EHA 2026

Syndax

Syndax

SNDX

0.00

  • Syndax highlighted new Revuforj (revumenib) data presented at EHA 2026, spanning real-world use, frontline combinations, post-transplant maintenance, and additional leukemia subtypes.
  • Across studies, revumenib produced high response rates in NPM1-mutated or KMT2A-rearranged acute leukemia, including deep remissions when combined with standard regimens.
  • Post-transplant use in a trial analysis showed strong survival outcomes, supporting a potential maintenance strategy to extend remission durability.
  • Data in NUP98-rearranged acute leukemia showed meaningful activity in a hard-to-treat population, expanding the drug’s commercial and clinical reach beyond its current core segments.
  • Safety findings were broadly consistent with the established profile, with no new signals highlighted in the EHA presentations.


Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Syndax Pharmaceuticals Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202606110703PRIMZONEFULLFEED9745489) on June 11, 2026, and is solely responsible for the information contained therein.