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Beigene Ltd ADR
(NQ:
BGNE
)
131.86
UNCHANGED
Streaming Delayed Price
Updated: 4:00 PM EDT, Apr 17, 2024
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Press Releases about Beigene Ltd ADR
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BeiGene Launches Proposed Initial Public Offering on the STAR Market in China
November 23, 2021
From
BeiGene, Ltd.
Via
Business Wire
BeiGene Closes on Property for New U.S. Manufacturing and Clinical R&D Center
November 23, 2021
From
BeiGene, Ltd.
Via
Business Wire
BeiGene Initiates First-in-Human Phase 1 Clinical Trial of Investigational TYK2 Inhibitor BGB-23339
November 22, 2021
From
BeiGene
Via
Business Wire
BeiGene and NewBridge Pharmaceuticals Announce Approval in Saudi Arabia of BRUKINSA® (Zanubrutinib) for the Treatment of Patients with Relapsed or Refractory Mantle Cell Lymphoma
November 14, 2021
From
BeiGene
Via
Business Wire
BeiGene Reports Third Quarter 2021 Financial Results
November 04, 2021
From
BeiGene, Ltd.
Via
Business Wire
BeiGene to Present Clinical Data on BRUKINSA in Chronic Lymphocytic Leukemia at the 63rd ASH Annual Meeting
November 04, 2021
From
BeiGene
Via
Business Wire
BeiGene and Nanolek Announce Approval in Russia for BRUKINSA® (Zanubrutinib) for Treatment of Patients with Relapsed or Refractory Mantle Cell Lymphoma
October 20, 2021
From
BeiGene
Via
Business Wire
BeiGene Announces BRUKINSA® (Zanubrutinib) Approved for Treatment of Patients with Mantle Cell Lymphoma in Australia
October 10, 2021
From
BeiGene
Via
Business Wire
BeiGene Announces First Regulatory Approval in Australia for BRUKINSA® (Zanubrutinib) for Treatment of Patients with Waldenström’s Macroglobulinemia
October 07, 2021
From
BeiGene
Via
Business Wire
BeiGene Announces Inclusion in FTSE Russell Indices
September 20, 2021
From
BeiGene, Ltd.
Via
Business Wire
BeiGene Receives Positive CHMP Opinion for BRUKINSA® (Zanubrutinib) for the Treatment of Adults with Waldenström’s Macroglobulinemia
September 17, 2021
From
BeiGene
Via
Business Wire
U.S. FDA Grants BRUKINSA® (Zanubrutinib) Accelerated Approval in Relapsed or Refractory Marginal Zone Lymphoma
September 15, 2021
From
BeiGene, Ltd.
Via
Business Wire
BeiGene Announces U.S. FDA Acceptance of Biologics License Application for Tislelizumab in Esophageal Squamous Cell Carcinoma
September 13, 2021
From
BeiGene, Ltd.
Via
Business Wire
BeiGene to Present Latest Findings in Robust Lung Cancer Portfolio at ESMO Congress 2021
September 12, 2021
From
BeiGene, Ltd.
Via
Business Wire
U.S. FDA Grants BRUKINSA® (Zanubrutinib) Approval in Waldenström’s Macroglobulinemia
September 01, 2021
From
BeiGene, Ltd.
Via
Business Wire
BeiGene Announces Acceptance of a Supplemental Biologics License Application in China for Tislelizumab in Nasopharyngeal Cancer
August 22, 2021
From
BeiGene, Ltd.
Via
Business Wire
BeiGene and EUSA Pharma Announce China NMPA Approval of QARZIBA® (Dinutuximab Beta) for Patients with High-Risk Neuroblastoma
August 17, 2021
From
BeiGene, Ltd.
Via
Business Wire
BeiGene to Host Investor Conference Call and Webcast to Discuss the Company’s Early Development Pipeline and Research on August 25, 2021
August 16, 2021
From
BeiGene, Ltd.
Via
Business Wire
BeiGene Reports Second Quarter 2021 Financial Results
August 05, 2021
From
BeiGene, Ltd.
Via
Business Wire
BeiGene Announces Plans to Build New Manufacturing and Clinical R&D Center at Princeton West Innovation Park in Hopewell, New Jersey
August 03, 2021
From
BeiGene, Ltd.
Via
Business Wire
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
July 29, 2021
From
BeiGene, Ltd.
Via
Business Wire
BeiGene Announces Approval in Canada of BRUKINSA® (Zanubrutinib) for the Treatment of Patients with Mantle Cell Lymphoma
July 26, 2021
From
BeiGene, Ltd.
Via
Business Wire
BeiGene Announces the Approval in China of KYPROLIS® (Carfilzomib) for Injection for Adult Patients with Relapsed or Refractory Multiple Myeloma
July 09, 2021
From
BeiGene, Ltd.
Via
Business Wire
BeiGene Announces Acceptance of a Supplemental Biologics License Application in China for Tislelizumab in Esophageal Squamous Cell Carcinoma (ESCC)
July 07, 2021
From
BeiGene, Ltd.
Via
Business Wire
China NMPA Approves Tislelizumab in Non-Small Cell Lung Cancer and Hepatocellular Carcinoma
June 23, 2021
From
BeiGene, Ltd.
Via
Business Wire
BeiGene Announces China NMPA Approval of BRUKINSA® (Zanubrutinib) for the Treatment of Patients with Relapsed or Refractory Waldenström’s Macroglobulinemia
June 18, 2021
From
BeiGene
Via
Business Wire
BeiGene Announces First Patient Dosed in Global Phase 3 Trial of Anti-TIGIT Antibody Ociperlimab in Non-Small Cell Lung Cancer
June 17, 2021
From
BeiGene, Ltd.
Via
Business Wire
BeiGene Presents Long-Term Efficacy and Safety Results from Three Pivotal Trials of BRUKINSA® (Zanubrutinib) and Tislelizumab at EHA2021
June 11, 2021
From
BeiGene, Ltd.
Via
Business Wire
BeiGene Presents ALPINE Results at EHA2021 Demonstrating Both Efficacy and Safety Advantages of BRUKINSA® (Zanubrutinib) in Head-to-Head Comparison to Ibrutinib in Chronic Lymphocytic Leukemia
June 11, 2021
From
BeiGene, Ltd.
Via
Business Wire
Shoreline Biosciences and BeiGene Announce Strategic Worldwide Collaboration to Develop and Commercialize Genetically Modified Natural Killer (NK) Cell Therapies
June 09, 2021
From
BeiGene, Ltd.
Via
Business Wire
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