Tuxobertinib (BDTX-189) is a potent, orally active and selective inhibitor of allosteric EGFR and HER2 oncogenic mutations, including EGFR/HER2 exon 20 insertion mutants. Tuxobertinib shows K D s of 0.2, 0.76, 13 and 1.2 nM for EGFR , HER2, BLK and RIPK2 , reapectively. Anticancer activity.
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