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BeiGene (BGNE) Announces Health Canada Approval for BRUKINSA
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BeiGene Announces Health Canada Approval for BRUKINSA® (zanubrutinib) in Relapsed or Refractory Marginal Zone Lymphoma
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BeiGene to Present at the Cowen 42nd Annual Health Care Virtual Conference
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BeiGene Reports Fourth Quarter and Full Year 2021 Financial Results
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BeiGene (BGNE) Announces European Medicines Agency Acceptance of Applications for BRUKINSA (zanubrutinib) in Chronic Lymphocytic Leukemia and Marginal Zone Lymphoma
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BeiGene (BGNE) Announces FDA Acceptance of Supplemental New Drug Application for BRUKINSA in Chronic Lymphocytic Leukemia
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BeiGene (BGNE) Announces FDA Acceptance of Supplemental New Drug Application for BRUKINSA in Chronic Lymphocytic Leukemia
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BeiGene Announces U.S. FDA Acceptance of Supplemental New Drug Application for BRUKINSA (zanubrutinib) in Chronic Lymphocytic Leukemia
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BeiGene Announces European Medicines Agency Acceptance of Applications for BRUKINSA (zanubrutinib) in Chronic Lymphocytic Leukemia and Marginal Zone Lymphoma
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BeiGene (BGNE) Announces Approval of BRUKINSA by Swissmedic for Treatment of Adult Patients with Waldenström’s Macroglobulinemia
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BeiGene Announces Approval for BRUKINSA (zanubrutinib) by Swissmedic for Treatment of Adult Patients with Waldenström’s Macroglobulinemia
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Drs. Margaret Dugan and Alessandro Riva Appointed to BeiGene Board of Directors
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BeiGene Announces Acceptance of Supplemental New Drug Application in China for BRUKINSA (zanubrutinib) in Chronic Lymphocytic Leukemia with Breakthrough Therapy Designation
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BeiGene (BGNE) Reports Positive Findings from Phase 3 Trial of Tislelizumab in Combination with Chemotherapy
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BeiGene Announces Positive Findings from Phase 3 Trial of Tislelizumab in Combination with Chemotherapy in First-Line Gastric or Gastroesophageal Junction Cancer
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BeiGene (BGNE) Announces Supplemental NDA for BRUKINSA in Waldenstrom’s Macroglobulinemia Accepted in China
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BeiGene Announces Acceptance of a Supplemental New Drug Application in China for BRUKINSA (zanubrutinib) in Waldenström’s Macroglobulinemia
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BeiGene Announces Launch of Bioisland Innovation Center
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BeiGene (BGNE) Announces UK Approval of BRUKINSA for Treatment of Adults with Waldenström’s Macroglobulinemia
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BeiGene Announces Authorisation of BRUKINSA (zanubrutinib) from the United Kingdom’s MHRA for the Treatment of Adults with Waldenström’s Macroglobulinemia in Great Britain
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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 China
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BeiGene (BGNE) Announces Updated Safety and Efficacy Findings on BRUKINSA in BTK Inhibitor-Intolerant Patients with Relapsed or Refractory B-Cell Malignancies
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BeiGene (BGNE) Reports Results from SEQUOIA Trial of BRUKINSA
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BeiGene Presents Results from SEQUOIA Trial of BRUKINSA (zanubrutinib) in First-Line Chronic Lymphocytic Leukemia at the 63rd ASH Annual Meeting
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BeiGene Presents Updated Safety and Efficacy Findings on BRUKINSA (zanubrutinib) in BTK Inhibitor-Intolerant Patients with Relapsed or Refractory B-Cell Malignancies
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BeiGene (BGNE) Presents Results from Phase 3 Trial of Tislelizumab in Nasopharyngeal Cancer at ESMO
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BeiGene Presents Results from Phase 3 Trial of Tislelizumab in Nasopharyngeal Cancer at ESMO Immuno-Oncology Congress 2021
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BeiGene (BGNE) and EUSA Pharma Announce Approval of SYLVANT in China for Idiopathic Multicentric Castleman Disease
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BeiGene and EUSA Pharma Announce NMPA Approval of SYLVANT® (Siltuximab for Injection) in China for Idiopathic Multicentric Castleman Disease
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BeiGene and EUSA Pharma Announce NMPA Approval of SYLVANT® (Siltuximab for Injection) in China for Idiopathic Multicentric Castleman Disease
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BeiGene to Present New Clinical Data on Tislelizumab at ESMO IO Congress 2021
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BeiGene (BGNE) Announces Pricing of its RMB22.2 billion (US$3.5 billion) IPO on the STAR Market of the Shanghai Stock Exchange in China
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BeiGene Announces Pricing of its RMB22.2 billion (US$3.5 billion) Initial Public Offering on the STAR Market of the Shanghai Stock Exchange in China
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BeiGene (BGNE) Announces Approval of BRUKINSA in European Union for Treatment of Adults with Waldenstrom's Macroglobulinemia
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BeiGene Announces Approval of BRUKINSA (zanubrutinib) in the European Union for Treatment of Adults with Waldenström’s Macroglobulinemia
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BeiGene (BGNE) Launches Proposed Initial Public Offering on the STAR Market in China
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BeiGene Launches Proposed Initial Public Offering on the STAR Market in China
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BeiGene Closes on Property for New U.S. Manufacturing and Clinical R&D Center
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BeiGene Initiates First-in-Human Phase 1 Clinical Trial of Investigational TYK2 Inhibitor BGB-23339
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BeiGene (BGNE) and NewBridge Receive Approval for BRUKINSA in Saudi Arabia
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BeiGene and NewBridge Pharmaceuticals Announce Approval in Saudi Arabia of BRUKINSA® (Zanubrutinib) for the Treatment of Patients with Relapsed or Refractory Mantle Cell Lymphoma
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BeiGene Reports Third Quarter 2021 Financial Results
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BeiGene to Present Clinical Data on BRUKINSA in Chronic Lymphocytic Leukemia at the 63rd ASH Annual Meeting
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BeiGene (BGNE) and Nanolek's BRUKINSA Approved in Russia for Treatment of Patients with Relapsed or Refractory Mantle Cell Lymphoma
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BeiGene and Nanolek Announce Approval in Russia for BRUKINSA® (Zanubrutinib) for Treatment of Patients with Relapsed or Refractory Mantle Cell Lymphoma
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BeiGene's (BGNE) BRUKINSA Approved for Treatment of Patients with Mantle Cell Lymphoma in Australia
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BeiGene Announces BRUKINSA® (Zanubrutinib) Approved for Treatment of Patients with Mantle Cell Lymphoma
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BeiGene Announces BRUKINSA® (Zanubrutinib) Approved for Treatment of Patients with Mantle Cell Lymphoma in Australia
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BeiGene (BGNE) Announces First Regulatory Approval in Australia for BRUKINSA for Treatment of Patients with Waldenstrom's Macroglobulinemia
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BeiGene Announces First Regulatory Approval in Australia for BRUKINSA® (Zanubrutinib) for Treatment of Patients with Waldenström’s Macroglobulinemia

