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Beigene Ltd ADR (NQ: BGNE )

160.59 +4.06 (+2.59%)
Streaming Delayed Price Updated: 3:13 PM EDT, May 2, 2024 Add to My Watchlist
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Press Releases about Beigene Ltd ADR

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BeiGene Presents Long-Term Efficacy and Safety Results from Three Pivotal Trials of BRUKINSA® (Zanubrutinib) and Tislelizumab at EHA2021
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
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
From BeiGene, Ltd.
Via Business Wire
BeiGene Announces Acceptance of a Supplemental Biologics License Application in China for Tislelizumab in Microsatellite Instability-High (MSI-H) or Mismatch Repair-Deficient (dMMR) Solid Tumors
From BeiGene, Ltd.
Via Business Wire
BeiGene Presents Clinical Data from Two Pivotal Trials of Tislelizumab at the 2021 ASCO Annual Meeting
From BeiGene, Ltd.
Via Business Wire
BeiGene Presents Clinical Data from Two Phase 2 Trials of Pamiparib at the 2021 ASCO Annual Meeting
From BeiGene, Ltd.
Via Business Wire
BeiGene Announces First Presentation of the Phase 3 ALPINE Trial Comparing BRUKINSA® (Zanubrutinib) to Ibrutinib in Chronic Lymphocytic Leukemia to Be Featured in Presidential Symposium at EHA2021
From BeiGene, Ltd.
Via Business Wire
BeiGene Announces Positive Topline Results from Phase 3 Trial of Tislelizumab in Combination with Chemotherapy as First-Line Treatment for Recurrent or Metastatic Nasopharyngeal Cancer
From BeiGene, Ltd.
Via Business Wire
BeiGene to Showcase Broad Clinical Portfolio at 2021 ASCO Annual Meeting
From BeiGene, Ltd.
Via Business Wire
BeiGene Announces U.S. FDA Acceptance and Priority Review of Supplemental New Drug Application for BRUKINSA® (Zanubrutinib) in Marginal Zone Lymphoma
From BeiGene, Ltd.
Via Business Wire
BeiGene Highlights Progress in Hematology at EHA2021 Virtual Congress
From BeiGene, Ltd.
Via Business Wire
China NMPA Approves PARP Inhibitor Pamiparib for Patients with Previously Treated Advanced Ovarian Cancer
From BeiGene, Ltd.
Via Business Wire
BeiGene Reports First Quarter 2021 Financial Results
From BeiGene, Ltd.
Via Business Wire
BRUKINSA® (Zanubrutinib) Demonstrates Superior Objective Response Rate by Investigator Assessment and Reduced Rates of Atrial Fibrillation or Flutter at Interim Analysis in Head-to-Head Trial Against Ibrutinib in Chronic Lymphocytic Leukemia
From BeiGene
Via Business Wire
BeiGene Presents Interim Analysis Results of RATIONALE 303 Trial of Tislelizumab in Second- or Third-Line Non-Small Cell Lung Cancer at the AACR Annual Meeting 2021
From BeiGene, Ltd.
Via Business Wire
BeiGene Presents Clinical Data on Sitravatinib in Combination with Tislelizumab at the AACR Annual Meeting 2021
From BeiGene, Ltd.
Via Business Wire
BeiGene Provides Update on Phase 2 Clinical Trial of Zanubrutinib in Patients with COVID-19-Related Pulmonary Distress
From BeiGene, Ltd.
Via Business Wire
BeiGene Launches BRUKINSA® (Zanubrutinib) in Canada for Patients with Waldenström’s Macroglobulinemia
From BeiGene, Ltd.
Via Business Wire
BeiGene Announces First Commercial Manufacturing Approval for Its State-of-the-Art Biologics Facility in Guangzhou, China
From BeiGene, Ltd.
Via Business Wire
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