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CAMBRIDGE, Mass. and BEIJING, China, June 18, 2020 (GLOBE NEWSWIRE) -- BeiGene, Ltd. (NASDAQ: BGNE; HKEX: 06160), a commercial-stage biotechnology company focused on developing and commercializing innovative molecularly-targeted and immuno-oncology drugs for the treatment of cancer, today announced that its marketing authorization application ...

(MAA) for BRUKINSA® (zanubrutinib) for the treatment of patients with Waldenström’s macroglobulinemia (WM) who have received at least one prior therapy or as first-line treatment for patients unsuitable for chemo-immunotherapy has been validated for regulatory review by the European Medicines Agency (EMA).

http://www.globenewswire.com/news-release/2020/06/18/2050036/0/en/BeiGene-Announces-European-Medicines-Agency-Acceptance-of-its-Marketing-Authorization-Application-for-BRUKINSA-Zanubrutinib-for-the-Treatment-of-Patients-with-Waldenstr%C3%B6m-s-Macrogl.html