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Articles published by BeiGene, Ltd.

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BeiGene Reports First Quarter 2023 Financial Results and Corporate Developments
From BeiGene, Ltd.
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BeiGene and SpringWorks Present Clinical Data on Lifirafenib, in Combination with Mirdametinib, in Patients with Advanced or Refractory Solid Tumors with MAPK Pathway Aberrations at the American Association for Cancer Research Annual Meeting 2023
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BeiGene Reports Fourth Quarter and Full Year 2022 Financial Results
From BeiGene, Ltd.
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BeiGene Reports Third Quarter 2022 Financial Results
From BeiGene, Ltd.
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BeiGene Reports Second Quarter 2022 Financial Results
From BeiGene, Ltd.
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BeiGene Strengthens European Presence With the Opening of Regional Office in Basel, Switzerland
From BeiGene, Ltd.
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BeiGene Reports First Quarter 2022 Financial Results
From BeiGene, Ltd.
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BeiGene Introduces Global Environmental, Social, and Governance Strategy
From BeiGene, Ltd.
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IRC Determines BRUKINSA® (Zanubrutinib) Demonstrates Superior Overall Response Rate Versus Ibrutinib in Final Response Analysis of ALPINE Trial in Chronic Lymphocytic Leukemia
From BeiGene, Ltd.
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BeiGene Reports Fourth Quarter and Full Year 2021 Financial Results
From BeiGene, Ltd.
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BeiGene to Present at the Guggenheim Healthcare Talks - 2022 Oncology Conference
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BeiGene to Present at the J.P. Morgan 40th Annual Healthcare Conference
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BeiGene Expands Collaboration with Novartis to Develop and Commercialize BeiGene’s TIGIT Inhibitor and Market Five Novartis Oncology Medicines in China Broad Markets
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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 and EUSA Pharma Announce NMPA Approval of SYLVANT® (Siltuximab for Injection) in China for Idiopathic Multicentric Castleman Disease
From BeiGene, Ltd.
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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 Launches Proposed Initial Public Offering on the STAR Market in China
From BeiGene, Ltd.
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BeiGene Closes on Property for New U.S. Manufacturing and Clinical R&D Center
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BeiGene Reports Third Quarter 2021 Financial Results
From BeiGene, Ltd.
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BeiGene Announces Inclusion in FTSE Russell Indices
From BeiGene, Ltd.
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U.S. FDA Grants BRUKINSA® (Zanubrutinib) Accelerated Approval in Relapsed or Refractory Marginal Zone Lymphoma
From BeiGene, Ltd.
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BeiGene Announces U.S. FDA Acceptance of Biologics License Application for Tislelizumab in Esophageal Squamous Cell Carcinoma
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BeiGene to Present Latest Findings in Robust Lung Cancer Portfolio at ESMO Congress 2021
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U.S. FDA Grants BRUKINSA® (Zanubrutinib) Approval in Waldenström’s Macroglobulinemia
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BeiGene Announces Acceptance of a Supplemental Biologics License Application in China for Tislelizumab in Nasopharyngeal Cancer
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BeiGene and EUSA Pharma Announce China NMPA Approval of QARZIBA® (Dinutuximab Beta) for Patients with High-Risk Neuroblastoma
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BeiGene to Host Investor Conference Call and Webcast to Discuss the Company’s Early Development Pipeline and Research on August 25, 2021
From BeiGene, Ltd.
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BeiGene Reports Second Quarter 2021 Financial Results
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BeiGene Announces Plans to Build New Manufacturing and Clinical R&D Center at Princeton West Innovation Park in Hopewell, New Jersey
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BeiGene Announces Positive Topline Results from Phase 3 SEQUOIA Trial Comparing BRUKINSA® (Zanubrutinib) to Bendamustine Plus Rituximab in Patients with Treatment-Naïve Chronic Lymphocytic Leukemia
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