We are a commercial stage oncology innovator seeking to develop first-in-class therapies in areas of significant unmet need such as acute leukemia and chronic graft-versus-host disease. Our team is committed to adhering to scientific excellence and dedicated to serving the patient community by delivering therapeutics that provide meaningful and differentiated clinical results and address urgent unmet need.
Treatment Pipeline
View PipelineRevumenib
Beyond its initial indication, Syndax is also investigating revumenib in other genetically defined acute leukemias such as those with an NPM1 mutation, where a pivotal trial is ongoing.
Explore MoreAxatilimab
In addition to its first indication, Syndax aims to investigate axatilimab in earlier lines of therapy in combination with standard of care agents and in potential indications such as idiopathic pulmonary fibrosis, where a Phase 2 clinical trial is ongoing.
Explore moreSyndax to Announce Third Quarter 2024 Financial Results and Host Conference Call and Webcast on November 5, 2024
Incyte and Syndax Announce New England Journal of Medicine Publication of Data from Pivotal AGAVE-201 Trial of Niktimvo™ (axatilimab-csfr) in Chronic Graft-Versus-Host Disease
Incyte and Syndax Announce U.S. FDA Approval of Niktimvo™ (axatilimab-csfr) for the Treatment of Chronic Graft-Versus-Host Disease (GVHD)
Syndax is proud to announce a major milestone that the U.S. Food and Drug Administration has approved Revuforj® (revumenib)!
Read Our Press ReleasePlease see Full Prescribing Information, including BOXED WARNING here.