20:54:48 EDT Wed 08 May 2024
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Q:BGNE - BEIGENE LTD SPON ADS EACH REPR 13 ORD SHS - Website unknown - click to update
Sym-XBid - AskLastChg%ChVol$Vol#TrOpen-Hi-LoYear Hi-LoLast TrNewsDelay
BGNE - Q5.0160.00·166.940.1164.44+3.882.4221.035,7954,117165.49  168.46  161.38247.495  126.968119:42:0106:0015 min RT 2¢

Recent Trades - Last 10 of 4117
Time ETExPriceChangeVolume
19:42:01Q164.604.0439
19:37:24Q163.462.901
19:37:24Q163.472.9110
16:20:00Q164.443.885
16:01:08Q164.443.88700
16:00:06Q164.443.8899
16:00:05Q164.443.885
16:00:05Q164.443.881
16:00:05Q164.443.88369
16:00:05Q164.443.88234

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Recent Bulletins
Date ETSymbolTypeHeadline
2024-05-08 06:00U:BGNENews ReleaseBeiGene Reports First Quarter 2024 Financial Results and Business Updates
2024-04-26 10:34U:BGNENews ReleaseBeiGene Demonstrates Global Progress in 2023 Responsible Business & Sustainability Report
2024-04-24 16:01U:BGNENews ReleaseGlobal Oncology Innovator BeiGene Highlights New Data across Hematology and Solid Tumor Portfolio at 2024 ASCO Annual Meeting
2024-04-23 06:00U:BGNENews ReleaseBeiGene Receives European Commission Approval for Tislelizumab as Treatment for Non-Small Cell Lung Cancer
2024-03-14 16:28U:BGNENews ReleaseBeiGene Receives FDA Approval for TEVIMBRA(TM) for the Treatment of Advanced or Metastatic Esophageal Squamous Cell Carcinoma After Prior Chemotherapy
2024-03-13 08:00U:BGNENews ReleaseFirst Doses of BRUKINSA(TM) provided to Patients with Chronic Lymphocytic Leukemia in Low- and Middle-Income Countries Under Collaboration of The Max Foundation, BeiGene, and the BeiGene Foundation
2024-03-07 17:19U:BGNENews ReleaseBeiGene Announces FDA Accelerated Approval of BRUKINSA for the Treatment of Relapsed or Refractory Follicular Lymphoma
2024-03-06 06:00U:BGNENews ReleaseBeiGene to Present Clinical and Preclinical Data from Broad Portfolio and Pipeline at AACR Annual Meeting 2024
2024-02-29 10:00U:BGNENews ReleaseBeiGene Announces New Efficacy Analysis Comparing BRUKINSA(TM) vs Acalabrutinib in Relapsed or Refractory Chronic Lymphocytic Leukemia
2024-02-28 08:05U:BGNENews ReleaseBeiGene to Present at Upcoming Investor Conferences
2024-02-27 06:00U:BGNENews ReleaseBeiGene's Biologics License Application for TEVIMBRA(TM) (tislelizumab) for First-Line Gastric or Gastroesophageal Junction Cancers Accepted by FDA
2024-02-26 06:00U:BGNENews ReleaseBeiGene Reports Fourth Quarter and Full Year 2023 Financial Results and Business Updates
2024-02-26 05:00U:BGNENews ReleaseBeiGene Receives Positive CHMP Opinion for Tislelizumab as Treatment for Non-Small Cell Lung Cancer
2024-01-23 06:00U:BGNENews ReleaseBeiGene Welcomes Experienced Life Sciences Executive Olivier Brandicourt to Board of Directors
2023-12-22 06:00U:BGNENews ReleaseFDA Approves Label Update for BRUKINSA ‚ ® (zanubrutinib) in Chronic Lymphocytic Leukemia (CLL)
2023-12-21 06:01U:BGNENews ReleaseBeiGene to Present at the 42nd Annual J.P. Morgan Healthcare Conference
2023-11-29 16:01U:BGNENews ReleaseBeiGene to Host ASH Investor Meeting in Person and via Webcast on December 10, 2023
2023-11-28 06:00U:BGNENews ReleaseBeiGene to Present New Data Highlighting Hematology Portfolio and Pipeline Strengths at ASH 2023
2023-11-21 06:00U:BGNENews ReleaseBeiGene and Ensem Therapeutics Announce Partnership to Advance Differentiated CDK2 Inhibitor
2023-11-17 06:00U:BGNENews ReleaseBeiGene Receives European Commission Approval for BRUKINSA ‚ ® (zanubrutinib) for the Treatment of Relapsed or Refractory Follicular Lymphoma