BeiGene Announces Acceptance of a Supplemental New Drug Application in China for BRUKINSA (zanubrutinib) in Waldenström's MacroglobulinemiaBusiness Wire • 01/20/22
China NMPA Approves Tislelizumab as Second- or Third-Line Treatment for Patients with Locally Advanced or Metastatic Non-Small Cell Lung CancerBusiness Wire • 01/06/22
Novartis Inks Option Agreement For BeiGene Anti-Cancer Therapy For Over $1 BillionBenzinga • 12/20/21
Novartis strengthens immunotherapy pipeline with option, collaboration and license agreement with BeiGene for TIGIT inhibitor ociperlimabGlobeNewsWire • 12/20/21
BeiGene Expands Collaboration with Novartis to Develop and Commercialize BeiGene's TIGIT Inhibitor and Market Five Novartis Oncology Medicines in China Broad MarketsBusiness Wire • 12/20/21
BeiGene Announces Authorisation of BRUKINSA (zanubrutinib) from the United Kingdom's MHRA for the Treatment of Adults with Waldenström's Macroglobulinemia in Great BritainBusiness Wire • 12/15/21
BeiGene Announces Closing of Its RMB22.2 Billion (US$3.5 Billion) Initial Public Offering on the STAR Market of the Shanghai Stock Exchange in ChinaBusiness Wire • 12/15/21
Nanjing Leads Biolabs and BeiGene Announce Worldwide License and Collaboration Agreement for LBL-007 Anti-LAG-3 Antibody; BeiGene Granted Exclusive Commercialization Rights Outside of ChinaBusiness Wire • 12/14/21
Here are the 10 U.S.-listed Chinese stocks with the greatest American ownership — and Alibaba's not one of themCNBC • 12/14/21
BeiGene Presents Results from SEQUOIA Trial of BRUKINSA (zanubrutinib) in First-Line Chronic Lymphocytic Leukemia at the 63rd ASH Annual MeetingBusiness Wire • 12/12/21
BeiGene Presents Updated Safety and Efficacy Findings on BRUKINSA (zanubrutinib) in BTK Inhibitor-Intolerant Patients with Relapsed or Refractory B-Cell MalignanciesBusiness Wire • 12/11/21
BeiGene Presents Results from Phase 3 Trial of Tislelizumab in Nasopharyngeal Cancer at ESMO Immuno-Oncology Congress 2021Business Wire • 12/10/21
BeiGene - EUSA Pharma's Siltuximab Approved In China For Multicentric Castleman DiseaseBenzinga • 12/03/21
BeiGene and EUSA Pharma Announce NMPA Approval of SYLVANT® (Siltuximab for Injection) in China for Idiopathic Multicentric Castleman DiseaseBusiness Wire • 12/03/21