BeiGene (BGNE) – Business Wire
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BeiGene Receives European Commission Approval for Tislelizumab as Treatment for Non-Small Cell Lung Cancer
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BeiGene Receives FDA Approval for TEVIMBRA® for the Treatment of Advanced or Metastatic Esophageal Squamous Cell Carcinoma After Prior Chemotherapy
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Pi Health Raises Over $30M in Series A to Revolutionize Cancer Care and Clinical Trials
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First Doses of BRUKINSA® provided to Patients with Chronic Lymphocytic Leukemia in Low- and Middle-Income Countries Under Collaboration of The Max Foundation, BeiGene, and the BeiGene Foundation
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BeiGene Announces FDA Accelerated Approval of BRUKINSA for the Treatment of Relapsed or Refractory Follicular Lymphoma
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BeiGene to Present Clinical and Preclinical Data from Broad Portfolio and Pipeline at AACR Annual Meeting 2024
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BeiGene Announces New Efficacy Analysis Comparing BRUKINSA® vs Acalabrutinib in Relapsed or Refractory Chronic Lymphocytic Leukemia
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BeiGene to Present at Upcoming Investor Conferences
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BeiGene’s Biologics License Application for TEVIMBRA® (tislelizumab) for First-Line Gastric or Gastroesophageal Junction Cancers Accepted by FDA
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BeiGene Reports Fourth Quarter and Full Year 2023 Financial Results and Business Updates
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BeiGene Receives Positive CHMP Opinion for Tislelizumab as Treatment for Non-Small Cell Lung Cancer
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BeiGene Welcomes Experienced Life Sciences Executive Olivier Brandicourt to Board of Directors
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FDA Approves Label Update for BRUKINSA® (zanubrutinib) in Chronic Lymphocytic Leukemia (CLL)
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BeiGene to Present at the 42nd Annual J.P. Morgan Healthcare Conference
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BeiGene to Host ASH Investor Meeting in Person and via Webcast on December 10, 2023
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BeiGene to Present New Data Highlighting Hematology Portfolio and Pipeline Strengths at ASH 2023
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BeiGene and Ensem Therapeutics Announce Partnership to Advance Differentiated CDK2 Inhibitor
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BeiGene Receives European Commission Approval for BRUKINSA® (zanubrutinib) for the Treatment of Relapsed or Refractory Follicular Lymphoma
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BeiGene Continues Global Growth with Third Quarter 2023 Financial Results and Business Updates
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BeiGene to Present at the Jefferies London Healthcare Conference
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BRUKINSA® Receives Positive Recommendation from NICE in U.K. for Adult Patients with Chronic Lymphocytic Leukemia
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BeiGene Announces the Phase 3 RATIONALE 315 Trial Met Primary Endpoints of Major Pathological Response Rate and Event-Free Survival for Tislelizumab Plus Chemotherapy in Patients with Resectable Non-S
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BeiGene Announces Late-Breaking Data at ESMO Showing Tislelizumab plus Chemotherapy Significantly Improved Overall Survival at Final Analysis in First-Line Advanced Gastric or Gastroesophageal Junctio
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BeiGene Presentations at ESMO 2023 Demonstrate Robust Clinical Strategy for Tislelizumab as Monotherapy and in Combination with Pipeline Assets
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BeiGene Receives Positive CHMP Opinion for BRUKINSA® (zanubrutinib) in Relapsed or Refractory Follicular Lymphoma
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BeiGene Announces Positive Regulatory Updates in Europe and the U.S. After Recently Regaining Global Rights for TEVIMBRA®
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BeiGene to Present at the Morgan Stanley 21st Annual Global Healthcare Conference
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BeiGene Accelerates Global Momentum with Strong Second Quarter 2023 Financial Results
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BeiGene Announces Positive CHMP Opinion for Tislelizumab as a Treatment for Advanced or Metastatic ESCC
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BeiGene Announces FDA Acceptance of sNDA for Fifth BRUKINSA® Indication
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BeiGene and DualityBio Announce Partnership to Advance Differentiated Antibody Drug Conjugate (ADC) Therapy for Solid Tumors
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BeiGene to Host Investor Research and Development Day in Person and via Webcast on July 18, 2023
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BeiGene to Vigorously Defend Patent Infringement Allegations by Pharmacyclics
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BeiGene Highlights Significant BRUKINSA® (zanubrutinib) Data at the 17th International Conference on Malignant Lymphoma
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BeiGene Highlights Promising Data from Blood Cancer Portfolio and Pipeline at the European Hematology Association Hybrid Congress
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BRUKINSA® Approved in Canada for the Treatment of Chronic Lymphocytic Leukemia
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BeiGene Presentations at the 2023 ASCO Annual Meeting Reinforce Promise Across Oncology Portfolio
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BeiGene to Present at Upcoming Investor Conferences
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The Max Foundation, BeiGene, and the BeiGene Foundation Announce Collaboration to Advance Health Equity by Providing Access to BRUKINSA® for the Treatment of Chronic Lymphocytic Leukemia in Low- and
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BeiGene Receives New Approvals for BRUKINSA® (zanubrutinib) in China
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BeiGene Reports First Quarter 2023 Financial Results and Corporate Developments
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BeiGene to Highlight Broad Oncology Portfolio at the 2023 ASCO Annual Meeting
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BeiGene Announces Goals Focused on Sustainable Growth and Workforce Diversity in New ESG Report
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BeiGene Announces Positive Phase 3 Tislelizumab Trial in Advanced Gastric or Gastroesophageal Junction Adenocarcinoma
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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 Assoc
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MapKure, BeiGene and SpringWorks Present Clinical Data on BGB-3245, a Selective Next-Generation B-RAF Inhibitor, in Adult Patients with Advanced or Refractory Solid Tumors at the American Association
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BeiGene Expands Presence in Latin America With Opening of Brazil Office
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BeiGene Appoints Julius Pryor III as First Global Head of Diversity and Health Equity
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BeiGene Enters New Phase to Expand US Manufacturing and R&D Footprint in New Jersey
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BeiGene Reports Fourth Quarter and Full Year 2022 Financial Results
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