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CHICAGO & OSAKA, Japan--(BUSINESS WIRE)--Takeda Pharmaceutical Company Limited (TSE:4502) today reported results from a Phase 1 study evaluating the safety, tolerability, and maximum tolerated dose (MTD) of MLN9708, the first investigational oral proteasome inhibitor in clinical trials. The study evaluated once a week oral dosing of single agent MLN9708 in patients with relapsed and/or refractory multiple myeloma (MM). These data were reported in an oral presentation during the annual meeting of the American Society of Clinical Oncology (ASCO), held May 31st to June 4th in Chicago, Illinois.
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