Two and a half months after its first US Food and Drug Administration approval for Incyte Corp.-partnered Niktimvo (axatilimab-csfr) in chronic graft-versus-host disease (GVHD), Syndax Pharmaceuticals Inc. announced $350m in new financing from Royalty Pharma plc on 4 November to fund the launches of Niktimvo and what may be Syndax’s second FDA approval this year, the menin inhibitor revumenib for KMT2A-rearranged (KMT2Ar) acute leukemias.
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Scrip for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?