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BeiGene Announces Approval of BRUKINSA (zanubrutinib) in the European Union for Treatment of Adults with Waldenström s Macroglobulinemia

BeiGene Receives Positive CHMP Opinion for BRUKINSA (Zanubrutinib) for the Treatment of Adults with Waldenström s Macroglobulinemia

BeiGene Receives Positive CHMP Opinion for BRUKINSA (Zanubrutinib) for the Treatment of Adults with Waldenström s Macroglobulinemia
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X4 Pharmaceuticals Announces Presentation of Positive Data from Ongoing Phase 1b Clinical Trial of Mavorixafor in Waldenström s Macroglobulinemia at EHA 2021

Robust decreases in serum IgM at low- and mid-doses suggest best-in-class potential for mavorixafor plus ibrutinib therapy in double-mutation Waldenström’s patients; meaningful increases in hemoglobin levels suggest reduction in cancer burden in bone marrow At 6 months, patients achieved median IgM level reductions of 60%-75%, with one patient achieving normal IgM, and two of four patients (50%) had >50% reduction in IgM from baseline e-Poster now available online; pre-recorded presentation by l

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