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Obrutinib is a small molecule drug candidate that acts as a Bruton's tyrosine kinase (BTK) inhibitor. It is structurally and mechanistically related to ibrutinib, but it is a distinct compound. Obrutinib has been developed for the treatment of B-cell malignancies such as chronic lymphocytic leukemia (CLL), mantle cell lymphoma (MCL), and other hematologic cancers. Like other BTK inhibitors, obrutinib works by irreversibly binding to the BTK enzyme, thereby blocking B-cell receptor signaling pathways essential for the survival and proliferation of malignant B cells.
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