http://www.twitter.comTwitter is a service for friends, family, and co-workers to communicate and stay connected through the exchange of quick, frequent answers to one simple question: What are you doing?
View Older Stories View More Recent Stories
-
BeiGene Announces First Regulatory Approval in Australia for BRUKINSA® (Zanubrutinib) for Treatment of Patients with Waldenström’s Macroglobulinemia
-
BeiGene Announces Inclusion in FTSE Russell Indices
-
BeiGene (BGNE) Announces Positive CHMP Opinion for BRUKINSA® (Zanubrutinib) for the Treatment of Adults with Waldenström’s Macroglobulinemia
-
BeiGene Receives Positive CHMP Opinion for BRUKINSA® (Zanubrutinib) for the Treatment of Adults with Waldenström’s Macroglobulinemia
-
BeiGene (BGNE) BRUKINSA® Granted Accelerated Approval in Relapsed or Refractory Marginal Zone Lymphoma
-
U.S. FDA Grants BRUKINSA® (Zanubrutinib) Accelerated Approval in Relapsed or Refractory Marginal Zone Lymphoma
-
BeiGene (BGNE) Announces U.S. FDA Acceptance of BLA for Tislelizumab in Esophageal Squamous Cell Carcinoma
-
BeiGene Announces U.S. FDA Acceptance of Biologics License Application for Tislelizumab in Esophageal Squamous Cell Carcinoma
-
BeiGene to Present Latest Findings in Robust Lung Cancer Portfolio at ESMO Congress 2021
-
BeiGene (BGNE) Granted FDA Approval for BRUKINSA to Treat WM
-
U.S. FDA Grants BRUKINSA® (Zanubrutinib) Approval in Waldenström’s Macroglobulinemia
-
BeiGene (BGNE) Announces Acceptance of Chinese Supplemental Biologics License Application for Tislelizumab
-
BeiGene Announces Acceptance of a Supplemental Biologics License Application in China for Tislelizumab in Nasopharyngeal Cancer
-
BeiGene Announces Acceptance by Swissmedic of Marketing Authorization Application for BRUKINSA® (Zanubrutinib) in Waldenström’s Macroglobulinaemia
-
BeiGene and EUSA Pharma Announce China NMPA Approval of QARZIBA® (Dinutuximab Beta) for Patients With High-Risk Neuroblastoma
-
BeiGene (BGNE) and EUSA Pharma Announce China NMPA Approval of QARZIBA® (Dinutuximab Beta) for Patients with High-Risk Neuroblastoma
-
BeiGene and EUSA Pharma Announce China NMPA Approval of QARZIBA® (Dinutuximab Beta) for Patients with High-Risk Neuroblastoma
-
BeiGene to Host Investor Conference Call and Webcast to Discuss the Company’s Early Development Pipeline and Research on August 25, 2021
-
BeiGene Reports Second Quarter 2021 Financial Results
-
BeiGene Announces Plans to Build New Manufacturing and Clinical R&D Center at Princeton West Innovation Park in Hopewell, New Jersey
-
BeiGene (BGNE) Announces Positive opline Results from Phase 3 SEQUOIA Trial of BRUKINSA® (Zanubrutinib)
-
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
-
BeiGene (BGNE) Announces Approval in Canada of BRUKINSA for the Treatment of Patients with Mantle Cell Lymphoma BGNE:
-
BeiGene Announces Approval in Canada of BRUKINSA® (Zanubrutinib) for the Treatment of Patients with Mantle Cell Lymphoma
-
BeiGene (BGNE) Announces the Approval in China of KYPROLIS for Injection for Adult Patients with R/R Multiple Myeloma
-
BeiGene Announces the Approval in China of KYPROLIS® (Carfilzomib) for Injection for Adult Patients with Relapsed or Refractory Multiple Myeloma
-
BeiGene Announces Acceptance of a Supplemental Biologics License Application in China for Tislelizumab in Esophageal Squamous Cell Carcinoma (ESCC)
-
PureTech (PRTC) Announces Clinical Trial and Supply Agreement with BeiGene (BGNE) to Evaluate LYT-200 and Tislelizumab in Patients with Difficult-to-Treat Solid Tumors
-
PureTech Announces Clinical Trial and Supply Agreement with BeiGene to Evaluate LYT-200 and Tislelizumab in Patients with Difficult-to-Treat Solid Tumors
-
BeiGene (BGNE) Announces China NMPA Approves Tislelizumab in Non-Small Cell Lung Cancer and Hepatocellular Carcinoma
-
China NMPA Approves Tislelizumab in Non-Small Cell Lung Cancer and Hepatocellular Carcinoma
-
BeiGene (BGNE) Announces China NMPA Approval of BRUKINSA for Treatment of Patients with Relapsed or Refractory Waldenstrom's Macroglobulinemia
-
BeiGene Announces China NMPA Approval of BRUKINSA® (Zanubrutinib) for the Treatment of Patients with Relapsed or Refractory Waldenström’s Macroglobulinemia
-
BeiGene Announces First Patient Dosed in Global Phase 3 Trial of Anti-TIGIT Antibody Ociperlimab in Non-Small Cell Lung Cancer
-
BeiGene Presents Long-Term Efficacy and Safety Results from Three Pivotal Trials of BRUKINSA® (Zanubrutinib) and Tislelizumab at EHA2021
-
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
-
Shoreline Biosciences and BeiGene Announce Strategic Worldwide Collaboration to Develop and Commercialize Genetically Modified Natural Killer (NK) Cell Therapies
-
BeiGene (BGNE) Announces Acceptance of sBLA in China for Tislelizumab in Microsatellite Instability-High or Mismatch Repair-Deficient Solid Tumors
-
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
-
BeiGene Presents Clinical Data from Two Pivotal Trials of Tislelizumab at the 2021 ASCO Annual Meeting
-
BeiGene Presents Clinical Data from Two Phase 2 Trials of Pamiparib at the 2021 ASCO Annual Meeting
-
BeiGene (BGNE) Announces First Presentation of Phase 3 ALPINE Trial Comparing BRUKINSA to Ibrutinib in Chronic Lymphocytic Leukemia to Be Featured in Presidential Symposium at EHA2021
-
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
-
BeiGene (BGNE) Reports Positive Topline Results from Phase 3 Trial of Tislelizumab
-
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
-
BeiGene to Showcase Broad Clinical Portfolio at 2021 ASCO Annual Meeting
-
BeiGene (BGNE) Announces U.S. FDA Acceptance and Priority Review of sNDA for BRUKINSA in Marginal Zone Lymphoma
-
BeiGene Announces U.S. FDA Acceptance and Priority Review of Supplemental New Drug Application for BRUKINSA® (Zanubrutinib) in Marginal Zone Lymphoma
-
BeiGene (BGNE) Highlights Progress in Hematology at EHA2021 Virtual Congress
-
BeiGene Highlights Progress in Hematology at EHA2021 Virtual Congress

