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Autor:
Padmaja Magadala, Joseph J. Buggy, Michelle Francesco, Lucy Jawed, Betty Chang, Stella Chang, Susanne M. Steggerda, Patricia Thiemann
Publikováno v:
Cancer Research. 73:923-923
Introduction: Ibrutnib is a potent and selective Btk inhibitor that covalently modifies Cys481 in Btk and inhibits B cell antigen receptor (BCR) signaling. Ibrutinib is currently in a Phase II study in patients with relapsed or refractory mantle cell