FDA Approves Pemigatinib for Patients With Myeloid/Lymphoid Neoplasms and FGFR1 Rearrangement

Last Updated: Monday, October 3, 2022

Based on data from the phase II, open-label, single-arm FIGHT-203 study, the U.S. Food and Drug Administration approved the selective fibroblast growth factor receptor (FGFR) inhibitor pemigatinib for the treatment of adults with relapsed or refractory myeloid/lymphoid neoplasms with FGFR1 rearrangement—extremely rare yet aggressive MPN subtypes.

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