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Beigene Ltd ADR
(NQ:
BGNE
)
138.99
+8.05 (+6.15%)
Official Closing Price
Updated: 4:15 PM EDT, Apr 23, 2024
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Press Releases about Beigene Ltd ADR
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BeiGene Expands Reach of its Innovative BTK Inhibitor with Recent Regulatory Approvals in Latin America
October 26, 2022
From
BeiGene
Via
Business Wire
BeiGene Receives Positive CHMP Opinion for BRUKINSA® (zanubrutinib) for the Treatment of Adults With CLL
October 14, 2022
From
BeiGene
Via
Business Wire
BeiGene Announces Positive Topline Results from Final Progression-Free Survival Analysis of BRUKINSA® (zanubrutinib) Compared to IMBRUVICA® (ibrutinib) in Phase 3 Chronic Lymphocytic Leukemia (CLL) Trial
October 12, 2022
From
BeiGene
Via
Business Wire
NICE Recommends BeiGene’s BRUKINSA® (zanubrutinib) for Patients with Waldenström’s Macroglobulinemia who have had at Least One Treatment
September 19, 2022
From
BeiGene
Via
Business Wire
BeiGene Receives Positive CHMP Opinion for BRUKINSA® (zanubrutinib) for the Treatment of Adults with Marginal Zone Lymphoma
September 19, 2022
From
BeiGene
Via
Business Wire
BeiGene Announces Data Presentations at ESMO 2022 Including Late-Breaking Oral Presentation for Tislelizumab in First-Line Unresectable Hepatocellular Cancer
September 10, 2022
From
BeiGene
Via
Business Wire
BeiGene to Present at the Morgan Stanley 20th Annual Global Healthcare Conference
September 07, 2022
From
BeiGene
Via
Business Wire
BeiGene Announces Acceptance of 11th Regulatory Submission for PD-1 Inhibitor Tislelizumab in China
August 23, 2022
From
BeiGene
Via
Business Wire
BeiGene Announces Strategic Alliance with Ontada to Improve U.S. Community Oncology Care
August 15, 2022
From
BeiGene
Via
Business Wire
BeiGene Announces Positive Global Phase 3 Trial Results for PD-1 Inhibitor Tislelizumab in First-Line Unresectable Hepatocellular Cancer
August 09, 2022
From
BeiGene
Via
Business Wire
BeiGene Reports Second Quarter 2022 Financial Results
August 04, 2022
From
BeiGene, Ltd.
Via
Business Wire
BeiGene Provides Regulatory Update on the U.S. Biologics License Application (BLA) for PD-1 Inhibitor Tislelizumab in 2L ESCC
July 14, 2022
From
BeiGene
Via
Business Wire
BeiGene Appoints Chan Lee as General Counsel
July 13, 2022
From
BeiGene
Via
Business Wire
BeiGene Announces Strategic Research Collaboration with InnoRNA to Jointly Discover Novel mRNA Therapies
July 06, 2022
From
BeiGene
Via
Business Wire
BeiGene Announces Late-Breaking Data at ESMO GI Showing Overall Survival Benefit for Tislelizumab Plus Chemotherapy in First-Line Advanced or Metastatic Esophageal Squamous Cell Carcinoma
June 30, 2022
From
BeiGene
Via
Business Wire
BeiGene Announces Acceptance of Supplemental Biologics License Application in China for Anti-PD-1 Inhibitor Tislelizumab
June 21, 2022
From
BeiGene
Via
Business Wire
BeiGene Announces BRUKINSA™ (zanubrutinib) Is Approved in 50 Markets
June 13, 2022
From
BeiGene
Via
Business Wire
BeiGene Announces PDUFA Goal Date Extension for U.S. sNDA for BRUKINSA for the Treatment of CLL/SLL
June 13, 2022
From
BeiGene
Via
Business Wire
BeiGene Highlights Growing Portfolio and Pipeline Targeting Hematologic Malignancies at European Hematology Association 2022 Congress
June 10, 2022
From
BeiGene
Via
Business Wire
China NMPA Approves Tislelizumab for Recurrent or Metastatic Nasopharyngeal Cancer
June 10, 2022
From
BeiGene
Via
Business Wire
BeiGene to Present at the Goldman Sachs 43rd Annual Global Healthcare Conference
June 08, 2022
From
BeiGene
Via
Business Wire
BeiGene Clinical Data Presentations at 2022 ASCO Annual Meeting Demonstrate Mature and Growing Oncology Portfolio
May 26, 2022
From
BeiGene
Via
Business Wire
BeiGene Strengthens European Presence With the Opening of Regional Office in Basel, Switzerland
May 17, 2022
From
BeiGene, Ltd.
Via
Business Wire
BeiGene to Demonstrate Strength of Hematology Portfolio and Pipeline at European Hematology Association 2022 Congress
May 12, 2022
From
BeiGene
Via
Business Wire
BeiGene Reports First Quarter 2022 Financial Results
May 05, 2022
From
BeiGene, Ltd.
Via
Business Wire
BeiGene Announces the Approval in China of BLINCYTO® (Blinatumomab) for Injection for Pediatric Patients with Relapsed or Refractory B-Cell Precursor Acute Lymphoblastic Leukemia (ALL)
May 04, 2022
From
BeiGene
Via
Business Wire
BeiGene Breaks Ground on New Manufacturing and Clinical R&D Center at the Princeton West Innovation Campus in New Jersey
April 29, 2022
From
BeiGene
Via
Business Wire
BeiGene Announces BRUKINSA (zanubrutinib) Approval in Uruguay in Mantle Cell Lymphoma, Marginal Zone Lymphoma, and Waldenström’s Macroglobulinemia
April 28, 2022
From
BeiGene
Via
Business Wire
BeiGene to Present Clinical Data from Innovative Oncology Portfolio at 2022 ASCO Annual Meeting
April 27, 2022
From
BeiGene
Via
Business Wire
Global Phase 3 Trial of BeiGene’s PD-1 Inhibitor, Tislelizumab, in Combination with Chemotherapy Meets Primary Endpoint in First-Line Advanced Esophageal Squamous Cell Carcinoma
April 27, 2022
From
BeiGene
Via
Business Wire
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