Resumen de acción HCM HUTCHMED (China) Limited, junto con sus filiales, descubre, desarrolla y comercializa terapias dirigidas e inmunoterapias para el cáncer y enfermedades inmunológicas en Hong Kong y a escala internacional. Saber más
Recompensas Análisis de riesgos No se han detectado riesgos en HCM a partir de nuestros controles de riesgos.
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Competidores de HUTCHMED (China) Limited Historial de precios y rendimiento
Resumen de las cotizaciones máximas, mínimas y variaciones del HUTCHMED (China) Precios históricos de las acciones Precio actual de la acción UK£13.56 Máximo en las últimas 52 semanas UK£21.92 Mínimo de 52 semanas UK£11.93 Beta 0.76 Cambio en 1 mes -5.17% Variación en 3 meses -34.96% Cambio de 1 año 3.20% Variación en 3 años -45.83% Variación en 5 años -44.77% Variación desde la OPV 0.44%
Noticias y actualizaciones recientes
Hutchmed Announces NMPA Full Approval for Orpathys (Savolitinib) in China for Patients with Locally Advanced or Metastatic Met Exon 14 NSCLC Jan 14 HUTCHMED (China) Limited Announces NDA Acceptance in China with Priority Review Status for ORPATHYS®? and TAGRISSO®? Combination in Lung Cancer Patients with MET amplication After Progression on First-Line EGFR Inhibitor Therapy Jan 02
Hutchmed (China) Limited Announces Breakthrough Therapy Designation in China for Orpathys®? and Tagrisso®? Combination in Certain Lung Cancer Patients After Disease Progression on Egfr Inhibitor Therapy Dec 12
HUTCHMED (China) Limited Announces Appointment of Chaohong Hu as Independent Non-Executive Director and Member of Technical Committee, Effective November 21, 2024 Nov 20
HUTCHMED (China) Limited Announces Positive High-Level Results from the SAVANNAH Phase II Trial Oct 16
Hutchmed (China) Limited Highlights Clinical Data to Be Presented at ESMO Congress 2024 and the 2024 World Conference of Lung Cancer Sep 09 Ver más actualizaciones
Hutchmed Announces NMPA Full Approval for Orpathys (Savolitinib) in China for Patients with Locally Advanced or Metastatic Met Exon 14 NSCLC Jan 14 HUTCHMED (China) Limited Announces NDA Acceptance in China with Priority Review Status for ORPATHYS®? and TAGRISSO®? Combination in Lung Cancer Patients with MET amplication After Progression on First-Line EGFR Inhibitor Therapy Jan 02
Hutchmed (China) Limited Announces Breakthrough Therapy Designation in China for Orpathys®? and Tagrisso®? Combination in Certain Lung Cancer Patients After Disease Progression on Egfr Inhibitor Therapy Dec 12
HUTCHMED (China) Limited Announces Appointment of Chaohong Hu as Independent Non-Executive Director and Member of Technical Committee, Effective November 21, 2024 Nov 20
HUTCHMED (China) Limited Announces Positive High-Level Results from the SAVANNAH Phase II Trial Oct 16
Hutchmed (China) Limited Highlights Clinical Data to Be Presented at ESMO Congress 2024 and the 2024 World Conference of Lung Cancer Sep 09
HUTCHMED Provides Update on Fruquintinib for Second-Line Gastric Cancer in China Aug 30
Hutchmed Growing Sales By 64% In H1 2024 Aug 09
HUTCHMED (China) Limited Provides Revenue Guidance for the Year 2024 Jul 31
HUTCHMED (China) Limited Announces NDA Acceptance in China for Tazemetostat for the Treatment of Relapsed or Refractory Follicular Lymphoma with Priority Review Jul 04
HUTCHMED (China) Limited to Report First Half, 2024 Results on Jul 31, 2024 Jun 26
Hutchmed Highlights Publication of Phase Iii Eslim-01 Results in the Lancet Haematology Jun 19
HUTCHMED (China) Limited Initiates Phase I Trial of Menin Inhibitor HMPL-506 in Patients with Hematological Malignancies in China Jun 08
HUTCHMED (China) Limited Highlights Publication of Phase III FRUTIGA Results in Nature Medicine Jun 05
HUTCHMED (China) Limited Highlights Presentations of New and Updated Data from Several Studies of Compounds Discovered by HUTCHMED At the Upcoming American Society of Clinical Oncology May 25 HUTCHMED (China) Limited Announces Executive Changes
HUTCHMED (China) Limited Initiates the RAPMichael Registrational Phase III Trial of HMPL-306 for Patients with IDH1- and/or IDH2-Mutated Relapsed/Refractory Acute Myeloid Leukemia in China May 15
HUTCHMED (China) Limited Initiates Phase II/III Trial of the Combination of Surufatinib and Camrelizumab for Treatment-Naive Pancreatic Ductal Adenocarcinoma in Collaboration with Hengrui May 14
HUTCHMED (China) Limited Appoints Dr. Renu Bhatia as an Independent Non-Executive Director and a Member of Technical Committee, Effective May 13, 2024 May 09
HUTCHMED (China) Limited, Annual General Meeting, May 10, 2024 Apr 09
HUTCHMED (China) Limited Highlights Data to be Presented at AACR Congress 2024 Apr 05
HUTCHMED and Innovent Jointly Announce NDA Acceptance in China for Fruquintinib Combination with Sintilimab for the Treatment of Advanced Endometrial Cancer with Priority Review Status Apr 03
HUTCHMED (China) Limited Announces Savolitinib sNDA Accepted in China for Treatment-Naive or Previously Treated Patients with Locally Advanced or Metastatic MET Exon 14 NSCLC Mar 28
Hutchmed Initiates Registration Stage of the Eslim-02 Phase Ii/Iii Trial of Sovleplenib for Warm Antibody Autoimmune Hemolytic Anemia in China Mar 22
Hutchmed Is Turning Profitable Mar 20
HUTCHMED (China) Limited Provides Revenue Guidance for the Year 2024 Feb 29
Hutchmed (China) Limited Highlights Presentation of Phase III Data on Fruquintinib in Second-Line Gastric Cancer At Asco Plenary Series Session Feb 07
HUTCHMED (China) Limited to Report Fiscal Year 2023 Results on Feb 28, 2024 Feb 01
HUTCHMED (China) Limited Receives Elunate® (Fruquintinib) Marketing Approval in Hong Kong for Treatment of Metastatic Colorectal Cancer Jan 30
HUTCHMED (China) Limited Announces NDA Acceptance in China for Sovleplenib for the Treatment of Primary Immune Thrombocytopenia with Priority Review Status Jan 11
HUTCHMED (China) Limited Completes Enrollment of a Phase II/III Trial of Fruquintinib in Combination with Sintilimab for Advanced Renal Cell Carcinoma in China Dec 13
Hutchmed (China) Limited Announces First in Human, Open-Label, Dose-Escalation Study of Erk1/2 Inhibitor Hmpl-295 in Patients with Advanced Solid Tumors Dec 01
HUTCHMED Announces that Takeda Receives U.S. FDA Approval of FRUZAQLA (fruquintinib) for Previously Treated Metastatic Colorectal Cancer Nov 09
HUTCHMED (China) Limited Announces Submission of New Drug Application for Fruquintinib for Previously Treated Metastatic Colorectal Cancer in Japan Oct 01
HUTCHMED (China) Limited Announces Presentation of Results from the Phase IIIb Trial of Savolitinib at the 2023 World Conference of Lung Cancer Sep 13
Hutchmed (China) Limited Completes Patient Enrollment of a Bridging Study of Tazemetostat in Patients with Relapsed/Refractory Follicular Lymphoma in China Sep 12
HUTCHMED Receives Breakthrough Therapy Designation in China for Savolitinib for Gastric Cancer Aug 29
HUTCHMED (China) Limited Announces the Sovleplenib Phase III ESLIM-01 Study Met its Primary Endpoint in Primary Immune Thrombocytopenia in China Aug 21
HUTCHMED (China) Limited Receives Breakthrough Therapy Designation in China for Fruquintinib Combination with Sintilimab for Treatment of Advanced Endometrial Cancer, and Completes Enrollment of Registration Study Jul 22
HUTCHMED (China) Limited Announces Changes to Board of Directors and Technical Committee Jul 14
Hutchmed (China) Limited Initiates Phase I Study of Its Novel SHP2 Inhibitor HMPL-415 for Advanced Malignant Solid Tumors in China Jul 12
HUTCHMED (China) Limited to Report First Half, 2023 Results on Jul 31, 2023 Jun 27 HUTCHMED (China) Limited and Takeda Announce Publication of Phase III FRESCO-2 Results in the Lancet Jun 17
Takeda and HUTCHMED Announce Marketing Authorization Application of Fruquintinib for Previously Treated Metastatic Colorectal Cancer Validated by the European Medicines Agency Jun 16
HUTCHMED (China) Limited and Takeda Announce New Drug Application (NDA) for Fruquintinib for Treatment of Previously Treated Metastatic Colorectal Cancer Granted Priority Review May 31
HUTCHMED (China) Limited Announces New and Updated Clinical Data Related to HUTCHMED May 26
HUTCHMED (China) Limited Appoints Solange Peters as Independent Non-Executive Director, Member of the Technical Committee and Member of the Audit Committee May 11
HUTCHMED (China) Limited to Report Fiscal Year 2022 Results on Feb 28, 2023 Jan 31
HUTCHMED (China) Limited Announces Agreement with NHSA for Inclusion of ORPATHYS in the National Reimbursement Drug List in China Jan 19
Hutchmed Completes Patient Enrollment of Eslim-01, A Phase Iii Trial of Sovleplenib in Primary Immune Thrombocytopenia in China Jan 04
HUTCHMED Initiates Rolling Submission of Nda to U.S. Fda for Fruquintinib for the Treatment of Refractory Colorectal Cancer Dec 20
HUTCHMED (China) Limited Announces Positive Topline Result in Fruquintinib Phase III FRUTIGA Study in Second-Line Gastric Cancer in China Nov 14
Hutchmed (China) Limited Initiates Phase 2/3 Trial of Fruquintinib Oct 28
HUTCHMED (China) Limited Initiates Phase II/III Trial of Sovleplenib for Warm Antibody Autoimmune Hemolytic Anemia in China Oct 11
Hutchmed begins dosing in phase 2/3 trial of sovleplenib for red blood cell disorder Oct 10
HUTCHMED (China) Limited Announces Summary Results of the 691-Patient, Multi-Regional Clinical Trial Sep 08
Inmagene Biopharmaceuticals and HUTCHMED (China) Limited Announce First Participant in Global Phase I Trial of IMG-004 Aug 10 HUTCHMED (China) Limited Announces that Fruquintinib Global Phase III FRESCO-2 Study Has Met Its Primary Endpoint in Metastatic Colorectal Cancer
Hutchmed, Inmagene begin dosing in phase 1 trial of potential autoimmune disease drug IMG-004 Aug 09
HUTCHMED (China) Limited Announces Fruquintinib Global Phase III FRESCO-2 Study in Metastatic Colorectal Cancer Aug 08
HUTCHMED (China) Limited Initiates A Bridging Study of Tazemetostat in Patients with Relapsed/Refractory Follicular Lymphoma in China Aug 01
Hutchmed begins dosing in mid-stage study of tazemetostat in blood cancer subtype Aug 01
HUTCHMED (China) Limited Initiates Phase I Trial of Anti-CD47 Monoclonal Antibody HMPL-A83 in Patients with Advanced Malignant Neoplasms in China Jul 16
Hutchmed begins dosing in early-stage study of cancer drug HMPL-A83 Jul 15
HUTCHMED (China) Limited Highlights First Presentation of Results of the SAVANNAH Global Phase II Trial of Savolitinib plus TAGRISSO® at the 2022 WCLC Annual Meeting Jul 13
Inmagene Biopharmaceuticals and HUTCHMED Announce First Participants in Global Phase I Trial of IMG-007 Jul 07
Hutchmed, Inmagene begin dosing in early-stage study of IMG-007 for eczema Jul 06
HUTCHMED (China) Limited to Report First Half, 2022 Results on Aug 01, 2022 Jun 08
HUTCHMED Announces TAZVERIK(R) Approved to be Used in Hainan Pilot Zone in China Jun 02
HUTCHMED (China) Limited Announces Board Changes May 18
Hutchmed Roils Markets With Changing Of Its Guard, U.S. Delisting Threat Mar 11 HUTCHMED (China) Limited Provides Revenue Guidance for the Year 2022
HUTCHMED (China) Limited Receives Approval to Commercialize Elunate in Macau Mar 03
HUTCHMED (China) Limited to Report Fiscal Year 2021 Final Results on Mar 03, 2022 Feb 08
HUTCHMED Initiates Phase Ib/II Study of HMPL-453 in Combination with Chemotherapy or Toripalimab for Advanced Solid Tumors in China Feb 05
HUTCHMED (China) Limited Initiates a Phase I Trial of HMPL-653 in Patients with Advanced Malignant Solid Tumors and TGCT in China Jan 20
HUTCHMED (China) Limited Update Analysis of Ongoing International Phase I/Ib Trial of Fruquintinib Jan 19
HUTCHMED (China) Limited Receives Breakthrough Therapy Designation in China for HMPL-523 for Treatment of Primary Immune Thrombocytopenia Jan 13
HUTCHMED Initiates Phase I Study of BTK Inhibitor HMPL-760 in Patients with Previously Treated B-Cell Non-Hodgkin Lymphoma in China Jan 10
Hutchmed (China) Limited Completes Planned Enrollment of FRESCO-2, A Global Phase III Trial of Fruquintinib in Metastatic Colorectal Cancer Dec 07
HUTCHMED (China) Limited and AstraZeneca PLC Initiate Sachi Phase III Trial of Orpathys® and Tagrisso® Combination in Certain Lung Cancer Patients in China After Progression on EGFR Inhibitor Therapy Nov 24 Rentabilidad de los accionistas HCM US Pharmaceuticals Mercado US 7D -4.5% 3.2% 1.9% 1Y 3.2% 3.2% 25.0%
Ver rendimientos de los accionistas
Rentabilidad vs. Industria: HCM igualó a la industria US Pharmaceuticals, que obtuvo un rendimiento del 3.2% el año pasado.
Rentabilidad vs. Mercado: HCM obtuvo unos resultados inferiores a los del mercado US, que fueron del 25% el año pasado.
Volatilidad de los precios Is HCM's price volatile compared to industry and market? HCM volatility HCM Average Weekly Movement 6.9% Pharmaceuticals Industry Average Movement 10.9% Market Average Movement 6.5% 10% most volatile stocks in US Market 19.1% 10% least volatile stocks in US Market 3.2%
Precio estable de las acciones: HCM no ha tenido una volatilidad de precios significativa en los últimos 3 meses en comparación con el mercado US.
Volatilidad a lo largo del tiempo: La volatilidad semanal de HCM (7%) se ha mantenido estable durante el año pasado.
Acerca de la empresa HUTCHMED (China) Limited, junto con sus filiales, descubre, desarrolla y comercializa terapias dirigidas e inmunoterapias contra el cáncer y las enfermedades inmunológicas en Hong Kong y a escala internacional. La empresa desarrolla Savolitinib para el tratamiento del cáncer de pulmón no microcítico (CPNM), el carcinoma papilar de células renales (CCR) y el cáncer gástrico (CG); y Fruquintinib, un inhibidor para el cáncer colorrectal (CCR), el cáncer de mama, el cáncer gástrico, el cáncer de endometrio (CMR) con estabilidad de microsatélites, el CPNM, el CCR, los tumores gastrointestinales, cervicales y sólidos. También desarrolla Surufatinib, que se utiliza para el tratamiento del tumor neuroendocrino pancreático (TNE), TNE no pancreático, carcinoma neuroendocrino, CPCP, cáncer del tracto biliar y tumores sólidos; y Sovleplenib que trata cánceres hematológicos y ciertas enfermedades inmunológicas crónicas.
Mostrar más Resumen de fundamentos de HUTCHMED (China) Limited ¿Cómo se comparan los beneficios e ingresos de HUTCHMED (China) con su capitalización de mercado? Estadísticas fundamentales de HCM Capitalización bursátil US$2.34b Beneficios(TTM ) -US$41.97m Ingresos (TTM ) US$610.81m
3.8x Ratio precio-ventas (PS)
-55.7x Ratio precio-beneficio (PE) Beneficios e Ingresos Estadísticas clave de rentabilidad del último informe de resultados (TTM) Cuenta de resultados (TTM ) de HCM Ingresos US$610.81m Coste de los ingresos US$658.26m Beneficio bruto -US$47.45m Otros gastos -US$5.48m Beneficios -US$41.97m
Últimos beneficios comunicados
Jun 30, 2024
Próxima fecha de beneficios
n/a
Beneficios por acción (BPA) -0.049 Margen bruto -7.77% Margen de beneficio neto -6.87% Ratio deuda/patrimonio 10.9%
¿Cómo se ha desempeñado HCM 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 2025/01/24 04:18 Precio de las acciones al final del día 2025/01/24 00:00 Beneficios 2024/06/30 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 HUTCHMED (China) Limited está cubierta por 49 analistas. 25 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 Jiangqiao Tong BOCI Research Ltd. Linda Lu BOCI Research Ltd. Alec Stranahan BofA Global Research
Mostrar 46 más analistas 
