TSE:4151Pharmaceuticals
Did Kyowa Kirin's (TSE:4151) New FDA Approval and Trials Just Shift Its Investment Narrative?
In the past week, Kyowa Kirin announced a series of product milestones, including FDA approval of KOMZIFTI (ziftomenib) for NPM1-mutated acute myeloid leukemia, new Japan launches of LUMICEF and Crysvita formulations, and the start of a Phase 3 achondroplasia study.
These developments reflect Kyowa Kirin’s focus on expanding its rare disease and oncology portfolios while enhancing treatment convenience and patient outcomes.
We'll explore how Kyowa Kirin's new ACHONDROPLASIA trial launch is...