Resumen de acción 6160 BeiGene, Ltd., empresa oncológica, se dedica a descubrir y desarrollar diversos tratamientos para pacientes con cáncer en Estados Unidos, China, Europa y a escala internacional. Saber más
Recompensas Análisis de riesgos Ver todos los controles de riesgos Captura tus ideas, enlaces y narrativas de la empresa
Competidores de BeiGene, Ltd. Historial de precios y rendimiento
Resumen de las cotizaciones máximas, mínimas y variaciones del BeiGene Precios históricos de las acciones Precio actual de la acción US$104.70 Máximo en las últimas 52 semanas US$153.00 Mínimo de 52 semanas US$75.45 Beta 0.60 Cambio en 1 mes -8.00% Variación en 3 meses -14.25% Cambio de 1 año 1.45% Variación en 3 años -34.97% Variación en 5 años 0.87% Variación desde la OPV -2.15%
Noticias y actualizaciones recientes
BeiGene, Ltd. Advances Leadership in CLL at ASH 2024 with New Data from Its Hematology Franchise Including BRUKINSA and Novel Pipeline Assets Dec 10
European Commission Approves BeiGene’s TEVIMBRA for First-Line Treatment of Advanced/Metastatic Esophageal Squamous Cell Carcinoma and Gastric or Gastroesophageal Junction Cancer Nov 27
BeiGene, Ltd. Announces Passing Away of Donald Glazer, A Board Member and the Chair of the Nominating and Corporate Governance Committee Oct 28
BeiGene, Ltd. to Report Q3, 2024 Results on Nov 13, 2024 Sep 30 BeiGene, Ltd. Appoints Shalini Sharp to Board of Directors and Member of the Audit Committee, Effective September 27, 2024 Sep 26
BeiGene Receives Israeli Ministry of Health Approval for TEVIMBRA® for the Treatment of Oesophageal Squamous Cell Carcinoma (OSCC) After Prior Chemotherapy Sep 17 Ver más actualizaciones
BeiGene, Ltd. Advances Leadership in CLL at ASH 2024 with New Data from Its Hematology Franchise Including BRUKINSA and Novel Pipeline Assets Dec 10
European Commission Approves BeiGene’s TEVIMBRA for First-Line Treatment of Advanced/Metastatic Esophageal Squamous Cell Carcinoma and Gastric or Gastroesophageal Junction Cancer Nov 27
BeiGene, Ltd. Announces Passing Away of Donald Glazer, A Board Member and the Chair of the Nominating and Corporate Governance Committee Oct 28
BeiGene, Ltd. to Report Q3, 2024 Results on Nov 13, 2024 Sep 30 BeiGene, Ltd. Appoints Shalini Sharp to Board of Directors and Member of the Audit Committee, Effective September 27, 2024 Sep 26
BeiGene Receives Israeli Ministry of Health Approval for TEVIMBRA® for the Treatment of Oesophageal Squamous Cell Carcinoma (OSCC) After Prior Chemotherapy Sep 17
BeiGene, Ltd. to Report Q2, 2024 Results on Aug 07, 2024 Jul 24
Beigene, Ltd. Appoints Aaron Rosenberg as the Principal Financial Officer, Effective from July 22, 2024 Jul 19
BeiGene, Ltd. Announces CFO Changes Jul 18
BeiGene, Ltd. to Report First Half, 2024 Results on Aug 30, 2024 Jun 28 BeiGene to Present New Data from SEQUOIA Study Evaluating BRUKINSA® plus Venetoclax in High-Risk First-Line CLL/SLL at EHA2024 BeiGene, Ltd. Announces New Analyses for BRUKINSA® (zanubrutinib) At ASCO Underscore Differentiated Clinical Profile for Treatment of CLL and SLL May 25
BeiGene Highlights New Hematology Portfolio and Pipeline Data at EHA2024 May 16
BeiGene, Ltd. Receives European Commission Approval for Tislelizumab as Treatment for Non-Small Cell Lung Cancer Apr 23
BeiGene, Ltd., Annual General Meeting, Jun 05, 2024 Apr 17
BeiGene, Ltd. to Report Q1, 2024 Results on May 11, 2024 Mar 29
BeiGene, Ltd. Receives FDA Approval for TEVIMBRA for Treatment of Advanced or Metastatic Esophageal Squamous Cell Carcinoma After Prior Chemotherapy Mar 15
BeiGene, Ltd. Announces FDA Accelerated Approval of BRUKINSA for the Treatment of Relapsed or Refractory Follicular Lymphoma Mar 08
BeiGene, Ltd. to Present Clinical and Preclinical Data from Broad Portfolio and Pipeline at AACR Annual Meeting 2024 Mar 06
BeiGene, Ltd. Receives Positive CHMP Opinion for Tislelizumab as Treatment for Non-Small Cell Lung Cancer Feb 28
BeiGene, Ltd. Announces Adults Living with Chronic Lymphocytic Leukemia in Ontario and Quebec Now Have Access, Through Public Reimbursement, to BRUKINSA® (Zanubrutinib) Jan 31
Beigene, Ltd. Announces Board Changes Jan 23
BeiGene, Ltd. Announces FDA Approves Label Update for BRUKINSA (zanubrutinib) in Chronic Lymphocytic Leukemia Dec 22
BeiGene, Ltd. Receives European Commission Approval for BRUKINSA®? (zanubrutinib) for the Treatment of Relapsed or Refractory Follicular Lymphoma Nov 18
Beigene, Ltd. Receives Positive Recommendation from Nice in U.K. for Adult Patients with Chronic Lymphocytic Leukemia Oct 21
BeiGene, Ltd. Presentations at ESMO 2023 Demonstrate Robust Clinical Strategy for Tislelizumab as Monotherapy and in Combination with Pipeli Oct 17
BeiGene Receives Positive CHMP Opinion for BRUKINSA®? (zanubrutinib) in Relapsed or Refractory Follicular Lymphoma Oct 15
BeiGene Receives Positive CHMP Opinion for BRUKINSA®? (zanubrutinib) in Relapsed or Refractory Follicular Lymphoma Oct 14
U.S. FDA Accepts Biologics License Application in First-Line Advanced ESCC Sep 22
BeiGene, Ltd. Announces Positive Regulatory Updates in Europe and the U.S. After Recently Regaining Global Rights for TEVIMBRA(R) Sep 20
Beigene, Ltd. Announces Change of Chair of Audit Committee Sep 15
Beigene Announces Positive CHMP Opinion for Tislelizumab as Treatment for Advanced or Metastatic ESCC Jul 23
Beigene, Ltd. Announces FDA Acceptance of sNDA for Fifth Brukinsa(R) Indication Jul 13
BeiGene, Ltd. to Report First Half, 2023 Results on Aug 30, 2023 Jun 28 BeiGene Highlights Significant Brukinsa® (Zanubrutinib) Data at 17th International Conference on Malignant Lymphoma
Pharmacyclics LLC Files Complaint Against Beigene, Ltd. and Beigene USA, Inc Jun 16
BeiGene Highlights Promising Data from Blood Cancer Portfolio and Pipeline at the European Hematology Association Hybrid Congress Jun 10
BeiGene, Ltd. Announces Approval of BRUKINSA (Zanubrutinib) by Health Canada for the Treatment of Adult Patients with Chronic Lymphocytic Leukemia May 31
BeiGene, Ltd. Announces Presentations At the 2023 ASCO Annual Meeting Reinforce Promise Across Oncology Portfolio May 26
Beigene, Ltd. Provides Update Regarding Recent Business Developments May 09
BeiGene Announces BRUKINSA Approved in the U.S. for Chronic Lymphocytic Leukemia Jan 21
Brukinsa (Zanubrutinib) Receives Marketing Authorization for Chronic Lymphocytic Leukemia and Marginal Zone Lymphoma in Great Britain by MHRA Jan 20
BeiGene Announces Expansion of Coverage on China’s National Reimbursement Drug List Jan 19
BeiGene, Ltd. Announces Center for Drug Evaluation of the China National Medical Products Administration Accepts Supplemental Biologics License Application Jan 07
BeiGene Announces Acceptance of 12th Regulatory Submission in China for PD-1 Inhibitor Tislelizumab Dec 31
Beigene, Ltd.'S Brukinsa Demonstrated Superior Progression-Free Survival over Imbruvica (Ibrutinib) in Chronic Lymphocytic Leukemia in Late-Breaker At ASH Dec 14
Beigene to Present Final Pfs Results from Alpine Trial Demonstrating Superior Pfs for Brukinsa® Versus Imbruvica® in Late-Breaking Oral Session At Ash 2022 Nov 23
Beigene, Ltd. Announces Change of Co-Chair of Scientific Advisory Committee Nov 22
BeiGene Receives European Commission Approval for Brukinsa® (Zanubrutinib) for the Treatment of Adults with Chronic Lymphocytic Leukemia (Cll) Nov 18
Beigene, Ltd. Announces Brazil Approvals for Brukinsa® as A Treatment for Rare Blood Cancers Nov 11
Abbisko Therapeutics Co., Ltd. Completes First Patient Enrollment in Phase II Clinical Trial for Investigational Pan-FGFR Inhibitor ABSK091 in Combination with Anti-PD-1 Antibody Tislelizumab Developed by BeiGene, Ltd. in Urothelial Carcinoma Nov 05
BeiGene Receives European Commission Approval for BRUKINSA(R) (zanubrutinib) for the Treatment of Adults with Marginal Zone Lymphoma Nov 03
BeiGene, Ltd. Expands Reach of its Innovative BTK Inhibitor with Recent Regulatory Approvals in Latin America Oct 27
BeiGene Receives Positive CHMP Opinion for BRUKINSA® (zanubrutinib) for the Treatment of Adults With CLL Oct 15
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 Oct 13 NICE Recommends Beigene’s BRUKINSA® (Zanubrutinib) for Patients with Waldenström’s Macroglobulinemia Who Have Had At Least One Treatment
Beigene, Ltd. Announces Appointment of Member of Compensation Committee Sep 15
BeiGene Announces Data Presentations at ESMO 2022 Including Late-Breaking Oral Presentation for Tislelizumab in First-Line Unresectable Hepatocellular Cancer Sep 10
BeiGene Announces Acceptance of 11th Regulatory Submission for PD-1 Inhibitor Tislelizumab in China Aug 24
BeiGene Announces Positive Global Phase 3 Trial Results for PD-1 Inhibitor Tislelizumab in First-Line Unresectable Hepatocellular Cancer Aug 10
Beigene Provides Regulatory Update on the U.S. Biologics License Application (Bla) for Pd 1 Inhibitor Tislelizumab in 2L Escc Jul 15
BeiGene, Ltd. Appoints Chan Lee as General Counsel, July 18 2022 Jul 14
Leap Therapeutics and BeiGene, Ltd. Announces Initiation of New DKN-01 Clinical Trials in Gastric Cancer, Colorectal Cancer and Endometrial Cancer Jul 13
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 Jul 01
Beigene, Ltd. Announces Executive Changes Jun 23
Beigene Announces Acceptance of Supplemental Biologics License Application in China for Anti-PD-1 Inhibitor Tislelizumab Jun 22 Ministry of Health in Kuwait Approves Beigene, Ltd.'s BRUKINSA™ (Zanubrutinib) in 50 Markets
BeiGene, Ltd. Announces NMPA Grants its Anti-PD-1 Antibody Tislelizumab Approval for First-Line Treatment of Patients with Advanced Non-Squamous Non-Small Cell Lung Cancer and Conditional Approval for Treatment of Patients with Hepatocellular Carcinoma Jun 11
Beigene Announces the Approval in China of BLINCYTO® for Injection for Pediatric Patients with Relapsed or Refractory B-Cell Precursor Acute Lymphoblastic Leukemia May 05
BeiGene, Ltd., Annual General Meeting, Jun 22, 2022 May 02
BeiGene to Present Clinical Data from Innovative Oncology Portfolio at 2022 ASCO Annual Meeting Apr 28
BeiGene, Ltd. to Report Q1, 2022 Results on May 05, 2022 Apr 22
BeiGene Presents Updated Results from Phase 3 RATIONALE-309 Trial of PD-1 Inhibitor Tislelizumab in First-Line RM-NPC in Virtual ASCO Plenary Series Apr 20
BeiGene, Ltd. Announces China National Medical Products Administration Approves Tislelizumab for Patients with Second-Line Esophageal Squamous Cell Carcinoma Apr 16
Beigene Announces IRC Determines Brukinsa® (Zanubrutinib) Demonstrates Superior Overall Response Rate Versus Ibrutinib in Final Response Analysis of ALPINE Trial in Chronic Lymphocytic Leukemia Apr 12
BeiGene to Present Clinical Results and Biomarker Data on Tislelizumab in Solid Tumors at the AACR Annual Meeting 2022 Apr 09
Beigene, Ltd. Announces European Medicines Agency Acceptance of Marketing Authorization Applications for Tislelizumab for the Treatment of Patients with ESCC and NSCLC Apr 07 BeiGene, Ltd. Announces Resignation of Jane Huang, Chief Medical Officer
BeiGene, Ltd. Announces Appointment of Margaret Han Dugan as Member of the Commercial and Medical Affairs Advisory Committee of its Board of Directors Mar 01
BeiGene Announces U.S. FDA Acceptance of Supplemental New Drug Application for BRUKINSA (zanubrutinib) in Chronic Lymphocytic Leukemia Feb 24
Beigene, Ltd. Announces Approval for Brukinsa (Zanubrutinib) by Swissmedic for Treatment of Adult Patients with Waldenström’s Macroglobulinemia Feb 18 BeiGene, Ltd. to Report Fiscal Year 2021 Final Results on Mar 31, 2022 BeiGene, Ltd. Announces Executive Changes Feb 05
BeiGene, Ltd. Announces Management Changes Feb 03
BeiGene, Ltd. Announces Board Appointments Feb 02
BeiGene Announces Acceptance of Supplemental New Drug Application in China for BRUKINSA (zanubrutinib) in Chronic Lymphocytic Leukemia with Breakthrough Therapy Designation Jan 30
BeiGene, Ltd. Announces Positive Findings from Phase 3 Trial of Tislelizumab in Combination with Chemotherapy in First-Line Gastric or Gastroesophageal Junction Cancer Jan 25
BeiGene Announces Acceptance of a Supplemental New Drug Application in China for BRUKINSA (zanubrutinib) in Waldenström’s Macroglobulinemia Jan 22
BeiGene, Ltd. Announces China NMPA Approves Tislelizumab as Second- or Third-Line Treatment for Patients with Locally Advanced or Metastatic Non-Small Cell Lung Cancer Jan 07
Beigene Presents Results from Sequoia Trial of Brukinsa (Zanubrutinib) in First-Line Chronic Lymphocytic Leukemia At the 63Rd Ash Annual Meeting Dec 13 Rentabilidad de los accionistas 6160 HK Biotechs Mercado HK 7D -3.4% -3.9% -0.5% 1Y 1.5% -5.7% 19.9%
Ver rendimientos de los accionistas
Rentabilidad vs. Industria: 6160 superó a la industria Hong Kong Biotechs, que obtuvo un rendimiento del -5.7% el año pasado.
Rentabilidad vs. Mercado: 6160 obtuvo unos resultados inferiores a los del mercado Hong Kong, que fueron del 19.9% el año pasado.
Volatilidad de los precios Is 6160's price volatile compared to industry and market? 6160 volatility 6160 Average Weekly Movement 6.6% Biotechs Industry Average Movement 11.1% Market Average Movement 8.8% 10% most volatile stocks in HK Market 18.6% 10% least volatile stocks in HK Market 4.1%
Precio estable de las acciones: 6160 no ha tenido una volatilidad de precios significativa en los últimos 3 meses.
Volatilidad a lo largo del tiempo: La volatilidad semanal de 6160 (7%) se ha mantenido estable durante el año pasado.
Acerca de la empresa BeiGene, Ltd., empresa oncológica, se dedica a descubrir y desarrollar diversos tratamientos para pacientes con cáncer en Estados Unidos, China, Europa y a escala internacional. Entre sus productos en fase comercial figuran BRUKINSA, una pequeña molécula inhibidora de la tirosina quinasa de Bruton (BTK) para el tratamiento de diversos cánceres sanguíneos; TEVIMBRA, una inmunoterapia con anticuerpos anti-PD-1 para el tratamiento de diversos tumores sólidos y cánceres sanguíneos; y PARTRUVIX, una pequeña molécula inhibidora selectiva de las enzimas PARP1 y PARP2 que se está evaluando como monoterapia y en combinaciones para el tratamiento de diversos tumores sólidos. Los productos en fase clínica de la empresa comprenden BGB-11417, un inhibidor de Bcl-2 de molécula pequeña; BGB-16673, un compuesto quimérico de activación de la degradación dirigido a BTK activo contra BTK de tipo salvaje y mutante; BGB-10188; BGB-21447, un inhibidor de Bcl-2; Ociperlimab (BGB-A1217), un inhibidor de TIGIT; Zanidatamab, un anticuerpo biespecífico dirigido a HER2; Surzebiclimab (BGB-A425), un inhibidor de TIM-3; BGB-A445, un anticuerpo agonista de OX40; BGB-15025, un inhibidor de molécula pequeña de HPK1; BGB-24714, un mimético de SMAC; BGB-26808, un inhibidor de HPK-1; Lifirafenib y BGB-3245, que son inhibidores de RAF; BGB-30813; BGB-A3055, un anticuerpo anti-CCR8; y BGB-43395, un inhibidor de CDK-4.
Mostrar más Resumen de fundamentos de BeiGene, Ltd. ¿Cómo se comparan los beneficios e ingresos de BeiGene con su capitalización de mercado? Estadísticas fundamentales de 6160 Capitalización bursátil HK$145.81b Beneficios(TTM ) -HK$6.39b Ingresos (TTM ) HK$25.05b
5.8x Ratio precio-ventas (PS)
-22.8x Ratio precio-beneficio (PE) Beneficios e Ingresos Estadísticas clave de rentabilidad del último informe de resultados (TTM) Cuenta de resultados (TTM ) de 6160 Ingresos CN¥23.51b Coste de los ingresos CN¥3.84b Beneficio bruto CN¥19.67b Otros gastos CN¥25.66b Beneficios -CN¥5.99b
Últimos beneficios comunicados
Sep 30, 2024
Próxima fecha de beneficios
n/a
Beneficios por acción (BPA) -56.41 Margen bruto 83.67% Margen de beneficio neto -25.50% Ratio deuda/patrimonio 29.6%
¿Cómo se ha desempeñado 6160 a largo plazo?
Ver rendimiento histórico y comparativa
Análisis de la empresa y estado de los datos financieros Datos Última actualización (huso horario UTC) Análisis de la empresa 2024/12/22 00:21 Precio de las acciones al final del día 2024/12/20 00:00 Beneficios 2024/09/30 Ingresos anuales 2023/12/31
Fuentes de datos Los datos utilizados en nuestro análisis de empresas proceden de S&P Global Market Intelligence LLC . Los siguientes datos se utilizan en nuestro modelo de análisis para generar este informe. Los datos están normalizados, lo que puede introducir un retraso desde que la fuente está disponible.
Paquete Datos Marco temporal Ejemplo Fuente EE.UU. * Finanzas de la empresa 10 años Cuenta de resultados Estado de tesorería Balance Estimaciones del consenso de analistas +3 años Previsiones financieras Objetivos de precios de los analistas Precios de mercado 30 años Precios de las acciones Dividendos, escisiones y acciones Propiedad 10 años Accionistas principales Información privilegiada Gestión 10 años Equipo directivo Consejo de Administración Principales avances 10 años
* ejemplo para los valores estadounidenses, para los no estadounidenses se utilizan formularios y fuentes normativas equivalentes.
A menos que se especifique lo contrario, todos los datos financieros se basan en un periodo anual, pero se actualizan trimestralmente. Esto se conoce como datos de los últimos doce meses (TTM) o de los últimos doce meses (LTM). Obtenga más información aquí .
Modelo de análisis y copo de nieve Los detalles del modelo de análisis utilizado para generar este informe están disponibles en nuestra página de Github , también tenemos guías sobre cómo utilizar nuestros informes y tutoriales en Youtube .
Conozca al equipo de talla mundial que diseñó y construyó el modelo de análisis Simply Wall St.
Métricas industriales y sectoriales Simply Wall St calcula cada 6 horas nuestras métricas sectoriales y de sección. Los detalles de nuestro proceso están disponibles en .
Fuentes analistas BeiGene, Ltd. está cubierta por 57 analistas. 29 de esos analistas presentaron las estimaciones de ingresos o ganancias utilizadas como datos para nuestro informe. Las estimaciones de los analistas se actualizan a lo largo del día.
Analista Institución Brian Skorney Baird Michael Meng BOCI Research Ltd. Yonglin Yan BOCI Research Ltd.
Mostrar 54 más analistas 
