BMY Aperçu des actions Bristol-Myers Squibb Company découvre, développe, concède sous licence, fabrique, commercialise, distribue et vend des produits biopharmaceutiques dans le monde entier. Plus de détails
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Bristol-Myers Squibb Company Concurrents Historique des prix et performances
Résumé des hausses, des baisses et des variations du cours de l'action pour la période du 1er janvier au 31 décembre 2009 Bristol-Myers Squibb Historique des cours de bourse Prix actuel de l'action US$54.24 Plus haut sur 52 semaines US$0 Plus bas sur 52 semaines US$0 Bêta 0.46 Variation sur 1 mois 0% Variation sur 3 mois 0% Variation sur 1 an 0% Variation sur 3 ans 22.19% Variation sur 5 ans 22.19% Évolution depuis l'introduction en bourse -0.75%
Nouvelles et mises à jour récentes
Bristol Myers Squibb Announces U.S. Food and Drug Administration Approves Opdivo Qvantig™? (nivolumab and Hyaluronidase-nvhy) Injection, for Subcutaneous Use in Most Previously Approved Adult, Solid Tumor Opdivo®? (Nivolumor Opdivo) Indications Dec 28 Bristol Myers Squibb Receives European Commission Approval for Opdivo® (nivolumab) Plus Yervoy® (ipilimumab) for the First-Line Treatment of Adult Patients with Microsatellite Instability-High or Mismatch Repair Deficient Metastatic Colorectal Cancer
Bristol-Myers Squibb Company to Report Q4, 2024 Results on Feb 06, 2025 Dec 19
Bristol Myers Squibb Company Declares Quarterly Dividend, Payable on February 3, 2025 Dec 12
Bristol Myers Squibb Highlights Progress of Cell Therapy Portfolio At Ash 2024 with Long-Term Survival Data and Results from Expanding Pipeline Dec 10
Bristol Myers Squibb’s Presentations at ASH 2024 Reinforce Strength of Hematology Portfolio and Scientific Advances in Differentiated Research Platforms Nov 20 Voir plus de mises à jour
Bristol Myers Squibb Announces U.S. Food and Drug Administration Approves Opdivo Qvantig™? (nivolumab and Hyaluronidase-nvhy) Injection, for Subcutaneous Use in Most Previously Approved Adult, Solid Tumor Opdivo®? (Nivolumor Opdivo) Indications Dec 28 Bristol Myers Squibb Receives European Commission Approval for Opdivo® (nivolumab) Plus Yervoy® (ipilimumab) for the First-Line Treatment of Adult Patients with Microsatellite Instability-High or Mismatch Repair Deficient Metastatic Colorectal Cancer
Bristol-Myers Squibb Company to Report Q4, 2024 Results on Feb 06, 2025 Dec 19
Bristol Myers Squibb Company Declares Quarterly Dividend, Payable on February 3, 2025 Dec 12
Bristol Myers Squibb Highlights Progress of Cell Therapy Portfolio At Ash 2024 with Long-Term Survival Data and Results from Expanding Pipeline Dec 10
Bristol Myers Squibb’s Presentations at ASH 2024 Reinforce Strength of Hematology Portfolio and Scientific Advances in Differentiated Research Platforms Nov 20
Bristol Myers Squibb Receives Positive CHMP Opinion for Repotrectinib for the Treatment of Advanced ROS1-Positive Non-Small Cell Lung Cancer and Advanced NTRK-Positive Solid Tumors Nov 16
Bristol-Myers Squibb Company Showcases the Continued Strength of Its Cardiovascular Portfolio with New Clinical and Real-World Data At American Heart Association Scientific Sessions 2024 Nov 12 Bristol Myers Squibb Presents New Long-Term Data from the EMERGENT Program Evaluating Covenfy in Adults with Schizophrenia At Psych Congress 2024
Bristol Myers Squibb to Present New Clinical and Health Economics and Outcomes Research Data At Psych Congress 2024 Oct 28
U.S. Food and Drug Administration Approves Perioperative Treatment of Neoadjuvant Opdivo® (nivolumab) and Chemotherapy Followed by Surgery and Adjuvant Single-Agent Opdivo for Resectable Non-Small Cell Lung Cancer (NSCLC) Oct 04
Bristol Myers Squibb Presents New Data from Two Trials Demonstrating Sotyktu (Deucravacitinib) Efficacy in Both Moderate-To-Severe Scalp Psoriasis and in A Real-World Setting Sep 29
U.S. Food and Drug Administration Approves Bristol Myers Squibb's COBENFY (xanomeline and Trospium Chlorx), a First-In-Class Muscarinic Agonist for the Treatment of Schizophrenia in Adults Sep 27 Bristol Myers Squibb Announces New Long-Term Zeposia (ozanimod) Data Demonstrate Durable Efficacy and Consistent Safety in Relapsing Forms of Multiple Sclerosis Sep 18
Bristol Myers Squibb Presents Landmark 10-Year Follow-Up Data from Checkmate -067 Which Showed Continued Durable Long-Term Survival Benefit with Opdivo® Plus Yervoy® in Advanced Melanoma Sep 16
Bristol-Myers Squibb Company to Report Q3, 2024 Results on Oct 31, 2024 Sep 12
Bristol Myers Squibb Announces Long-Term Follow-Up Data from Phase 3 Study of CAMZYOS (Mavacamten) Underscores Established Efficacy and Safety Profile in Patients with Symptomatic Obstructive Hypertrophic Cardiomyopathy (oHCM) Sep 02
Bristol Myers Squibb Receives U.S. Food and Drug Administration sBLA Acceptance for First-Line Treatment of Unresectable Hepatocellular Carcinoma Aug 21 European Medicines Agency Validates Bristol Myers Squibb's Application for CAR T Cell Therapy Breyanzi for Relapsed or Refractory Follicular Lymphoma Aug 19
Bristol-Myers Squibb Company Announces Intangible Asset Impairment Charges for the Three Months Ended June 30, 2024 Jul 26
Bristol Myers Squibb Receives European Medicines Agency Validation of Application for Opdivo (Nivolumab) Plus Yervoy (Ipilimumab) for First-Line Treatment of Unresectable or Advanced Hepatocellular Carcinoma Jul 20
Bristol Myers Squibb Announces U.S. FDA Accelerated Approval of KRAZATI®? (adagrasib) in Combination with Cetuximab for Adult Patients with Previously Treated KRAS G12C-Mutated Locally Advanced or Metastatic Colorectal Cancer (CRC) Jun 22 Bristol-Myers Squibb Company to Report Q2, 2024 Results on Jul 26, 2024
First quarter dividend of US$0.60 announced Jun 20
Bristol Myers Squibb Appoints Michael R. McMullen as Independent Director and Member of the Audit Committee, Effective July 1, 2024 Jun 19 Bristol Myers Squibb Declares A Quarterly Dividend, Payable on August 1, 2024 Jun 18
Bristol Myers Squibb Announces Opdivo (Nivolumab) Plus Yervoy (Ipilimumab) Significantly Improved Overall Survival Compared to Lenvatinib or Sorafenib as First-Line Treatment for Patients with Advanced Hepatocellular Carinoma in Checkmate -9DW Trial Jun 06 Bristol Myers Squibb’S Breyanzi Demonstrates Clinically Meaningful Outcomes Across Broad Range of B-Cell Malignancies in New Data Presented At 2024 Asco® Annual Meeting
U.S. Food and Drug Administration Approves Bristol Myers Squibb’s Breyanzi as a New CAR T Cell Therapy for Relapsed or Refractory Mantle Cell Lymphoma Jun 01
Bristol Myers Squibb Receives European Commission Approval for Opdivo (nivolumab) in Combination with Cisplatin and Gemcitabine May 30
Bristol Myers Squibb Announces New Four-Year Results from the POETYK PSO Long-Term Extension Trial of Sotyktu (Deucravacitinib) Treatment in Adult Patients with Moderate-To-Severe Plaque Psoriasis May 18 Bristol Myers Squibb's CAR T Cell Therapy Breyanzi Approves by the U.S. Food and Drug Administration for Relapsed or Refractory Follicular Lymphoma May 17
Bristol Myers Squibb Provides Update on Phase 3 CheckMate -73L Trial May 11
U.S. Food and Drug Administration Accepts Bristol Myers Squibb’s Application for Subcutaneous Nivolumab (nivolumab and hyaluronidase) May 08
European Medicines Agency Validates Bristol Myers Squibb’s Application for Opdivo (nivolumab) Plus Yervoy (ipilimumab) for the First-Line Treatment of Adult Patients with Microsatellite Instability–High or Mismatch Repair Deficient Metastatic Colorectal Cancer May 07
CHMP Adopts Positive Opinion Recommending Approval of Bristol Myers Squibb's Opdivo (nivolumab) in Combination with Cisplatin and Gemcitabine for the First-Line Treatment of Adult Patients with Unresectable or Metastatic Urothelial Carcinoma Apr 27
First quarter 2024 earnings released: US$5.89 loss per share (vs US$1.08 profit in 1Q 2023) Apr 25
Bristol Myers Squibb Announces KRAZATI (adagrasib) in Combination with Cetuximab Demonstrates Clinically Meaningful Activity as a Targeted Treatment Option for Patients with Previously Treated KRAS G12C-Mutated Locally Advanced or Metastatic Colorectal Cancer (CRC) Apr 10
U.S. Fda Approves Bristol Myers Squibb and 2Seventy Bio’S Abecma for Triple-Class Exposed Relapsed or Refractory Multiple Myeloma After Two Prior Lines of Therapy Apr 06
European Commission Expands Approval of Bristol Myers Squibb’S Reblozyl® (Luspatercept) Apr 03 Bristol Myers Squibb Provides Update on the First Phase 3 YELLOWSTONE Trial Evaluating Oral Zeposia (Oozanimod) in Patients with Moderate to Severe Active Crohn's Disease
Upcoming dividend of US$0.60 per share Mar 28
Bristol Myers Squibb to Present Data at the American College of Cardiology Annual Scientific Session 2024 Mar 27 Bristol Myers Squibb’s Abecma (idecabtagene vicleucel) Becomes First CAR T Cell Therapy Approved in the European Union in Earlier Lines for Triple-Class Exposed Relapsed and Refractory Multiple Myeloma
Bristol-Myers Squibb Company, Annual General Meeting, May 07, 2024 Mar 19 Bristol-Myers Squibb Company (NYSE:BMY) completed the acquisition of Karuna Therapeutics, Inc. (NasdaqGM:KRTX) from Capital International Investors, FMR LLC, The Vanguard Group, Inc., T. Rowe Price Group, Inc. (NasdaqGS:TROW) and others. Mar 18
FDA Advisory Committee Votes in Favor of Bristol-Myers Squibb Company and 2seventy bio, Inc. Abecma for Triple-Class Exposed Multiple Myeloma in Further Lines of Therapy Mar 16
U.S. FDA Approves Bristol Myers Squibb’s Breyanzi® as the First and Only CAR T Cell Therapy for Adults with Relapsed or Refractory Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma Mar 15
Bristol-Myers Squibb Company to Report Q1, 2024 Results on Apr 25, 2024 Mar 12
Fourth quarter dividend of US$0.60 announced Mar 11
U.S. Food and Drug Administration Approves Bristol-Myers Squibb Company's Opdivo Mar 08
Bristol-Myers Squibb Company (NYSE:BMY) completed the acquisition of RayzeBio, Inc. (NasdaqGM:RYZB). Feb 27 Bristol-Myers Squibb Company (NYSE:BMY) completed the acquisition of RayzeBio, Inc. (NasdaqGM:RYZB). Feb 26
Bristol Myers Squibb Receives Positive CHMP Opinion for Reblozyl® (luspatercept) for Treatment of Adults with Transfusion-Dependent Anemia due to Low- to Intermediate-Risk Myelodysplastic Syndromes (MDS) Feb 23
Bristol Myers Squibb Announces U.S. Food and Drug Administration (FDA) Accepts for Priority Review the Supplemental New Drug Application (sNDA) for KRAZATI (adagrasib) in Combination with Cetuximab for the Treatment of Patients with Previously Treated KRASG12C-Mutated Locally Advanced or Metastatic Colorectal Cancer Feb 22
Bristol-Myers Squibb Company Announces Management Changes Feb 16
U.S. Food and Drug Administration Accepts for Priority Review Bristol Myers Squibb's Application for Augtyro (repotrectinib) for the Treatment of Patients with NTRK-Positive Locally Advanced or Metastatic Solid Tumors Feb 15
Bristol Myers Squibb Announces Acceptance of U.S. and EU Regulatory Filings for Neoadjuvant Opdivo (nivolumab) and Chemotherapy Followed by Surgery and Adjuvant Opdivo in Resectable Non-Small Cell Lung Cancer Feb 10
Bristol Myers Squibb and 2seventy bio, Inc. Share Update on U.S. FDA Oncologic Drugs Advisory Committee Meeting for Abecma in Triple-Class Exposed Multiple Myeloma Based on KarMMa-3 Study Feb 06
Full year 2023 earnings released: EPS: US$3.88 (vs US$2.97 in FY 2022) Feb 02
Bristol-Myers Squibb Company Announces Three Regulatory Acceptances from the U.S. Food and Drug Administration (FDA) and Japan’S Ministry of Health, Labour and Welfare (MHLW) for Breyanzi Jan 31
Bristol Myers Squibb Announces the First Disclosure of Data from the Phase 3 CheckMate -67T Trial Jan 28
Bristol-Myers Squibb Company Receives Positive Chmp Opinion for Car T Cell Therapy Abecma (Idecabtagene Vicleucel) in Earlier Lines of Therapy for Triple-Class Exposed Relapsed and Refractory Multiple Myeloma Jan 26 Bristol Myers Squibb and Exelixis, Inc. Announce Four-Year Follow-Up Results from the CheckMate -9ER Trial Evaluating Opdivo (cabozantinib) Bristol-Myers Squibb Company (NYSE:BMY) completed the acquisition of Mirati Therapeutics, Inc. (NasdaqGS:MRTX) from a group of shareholders. Jan 23
Bristol Myers Squibb Announces Results from the Phase 3 Randomized Trial Evaluating Opdivo (nivolumab) Plus Yervoy (ipilimumab) Jan 21
Bristol Myers Squibb Data At Asco Gu 2024 Showcase Transformative Research in the Treatment of Genitourinary Cancers Jan 17
European Medicines Agency Validates Bristol Bristol-Myers Squibb Company Application for Repotrectinib for the Treatment of Locally Advanced or Metastatic Ros1-Positive Non-Small Cell Lung Cancer and Ntrk-Positive Solid Tumors Jan 02
Upcoming dividend of US$0.60 per share at 4.7% yield Dec 28
Bristol-Myers Squibb Company (NYSE:BMY) entered into definitive merger agreement to acquire RayzeBio, Inc. (NasdaqGM:RYZB) for $3.8 billion. Dec 27
Bristol-Myers Squibb Company (NYSE:BMY) entered into a definitive merger agreement to acquire Karuna Therapeutics, Inc. (NasdaqGM:KRTX) for $12.6 billion. Dec 23 Rendement pour les actionnaires BMY CH Pharmaceuticals CH Marché 7D 0% 1.5% 1.0% 1Y 0% 0.6% 2.3%
Voir le rapport complet des actionnaires
Rendement vs Industrie: BMY a sous-performé le secteur Swiss Pharmaceuticals qui a rapporté 0.6 % au cours de l'année écoulée.
Rendement vs marché: BMY a sous-performé le marché Swiss qui a rapporté 2.3 % au cours de l'année écoulée.
Volatilité des prix Is BMY's price volatile compared to industry and market? BMY volatility BMY Average Weekly Movement n/a Pharmaceuticals Industry Average Movement 2.9% Market Average Movement 3.3% 10% most volatile stocks in CH Market 7.7% 10% least volatile stocks in CH Market 1.6%
Cours de l'action stable: BMY n'a pas connu de volatilité de prix significative au cours des 3 derniers mois.
Volatilité au fil du temps: Données insuffisantes pour déterminer l'évolution de la volatilité de BMY au cours de l'année écoulée.
À propos de l'entreprise Fondée Salariés PDG Site web 1887 34,100 Chris Boerner www.bms.com
Bristol-Myers Squibb Company découvre, développe, concède sous licence, fabrique, commercialise, distribue et vend des produits biopharmaceutiques dans le monde entier. Elle propose des produits pour l'hématologie, l'oncologie, les maladies cardiovasculaires, l'immunologie, la fibrose et les neurosciences. Les produits de la société comprennent Eliquis pour la réduction du risque d'accident vasculaire cérébral/embolie systémique en cas de fibrillation auriculaire non valvulaire, et pour le traitement de la TVP/de l'EP ; Opdivo pour diverses indications anticancéreuses, y compris la vessie, le sang, le CCR, la tête et le cou, le RCC, le HCC, le poumon, le mélanome, le MPM, l'estomac et le cancer de l'œsophage ; Pomalyst/Imnovid pour le myélome multiple ; Orencia pour la polyarthrite rhumatoïde active et l'arthrite psoriasique ; et Sprycel pour le traitement de la leucémie myéloïde chronique à chromosome Philadelphie positif.
Afficher plus Bristol-Myers Squibb Company Résumé des fondamentaux Comment les bénéfices et les revenus de Bristol-Myers Squibb se comparent-ils à sa capitalisation boursière ? BMY statistiques fondamentales Capitalisation boursière CHF 84.96b Bénéfices(TTM) -CHF 5.54b Recettes(TTM ) CHF 39.38b
Bénéfices et recettes Principales statistiques de rentabilité tirées du dernier rapport sur les bénéfices (TTM) BMY compte de résultat (TTM ) Recettes US$46.51b Coût des recettes US$11.08b Marge brute US$35.43b Autres dépenses US$41.97b Les revenus -US$6.54b
Derniers bénéfices déclarés
Jun 30, 2024
Prochaine date de publication des résultats
Oct 31, 2024
Résultat par action (EPS) -3.23 Marge brute 76.18% Marge bénéficiaire nette -14.06% Ratio dettes/capitaux propres 306.9%
Quelles ont été les performances à long terme de BMY?
Voir les performances historiques et les comparaisons Dividendes
4.8% Rendement actuel des dividendes
-74% Ratio de distribution Quand faut-il acheter BMY pour recevoir un dividende à venir ? Bristol-Myers Squibb dates des dividendes Date ex-dividende Oct 04 2024 Date de paiement du dividende Nov 01 2024 Jours jusqu'au dividende Ex 91 days Jours jusqu'à la date de paiement du dividende 63 days
Analyse de l'entreprise et données financières Données Dernière mise à jour (heure UTC) Analyse de l'entreprise 2024/09/18 08:28 Cours de l'action en fin de journée 2024/06/21 00:00 Les revenus 2024/06/30 Revenus annuels 2023/12/31
Sources de données Les données utilisées dans notre analyse de l'entreprise proviennent de S&P Global Market Intelligence LLC . Les données suivantes sont utilisées dans notre modèle d'analyse pour générer ce rapport. Les données sont normalisées, ce qui peut entraîner un délai avant que la source ne soit disponible.
Paquet Données Cadre temporel Exemple de source américaine * Finances de l'entreprise 10 ans Compte de résultat Tableau des flux de trésorerie Bilan Estimations consensuelles des analystes +3 ans Prévisions financières Objectifs de prix des analystes Prix du marché 30 ans Cours des actions Dividendes, scissions et actions Propriété 10 ans Actionnaires principaux Délits d'initiés Gestion 10 ans L'équipe dirigeante Conseil d'administration Principaux développements 10 ans
* exemple pour les titres américains, pour les titres non-américains des formulaires et sources réglementaires équivalents sont utilisés.
Sauf indication contraire, toutes les données financières sont basées sur une période annuelle mais mises à jour trimestriellement. C'est ce qu'on appelle les données des douze derniers mois (TTM) ou des douze derniers mois (LTM). Pour en savoir plus , cliquez ici .
Modèle d'analyse et flocon de neige Les détails du modèle d'analyse utilisé pour générer ce rapport sont disponibles sur notre page Github . Nous avons également des guides sur la façon d'utiliser nos rapports et des tutoriels sur Youtube .
Découvrez l'équipe de classe mondiale qui a conçu et construit le modèle d'analyse Simply Wall St.
Indicateurs de l'industrie et du secteur Nos indicateurs de secteur et de section sont calculés toutes les 6 heures par Simply Wall St. Les détails de notre processus sont disponibles sur .
Sources des analystes Bristol-Myers Squibb Company est couverte par 51 analystes. 23 de ces analystes ont soumis les estimations de revenus ou de bénéfices utilisées comme données d'entrée dans notre rapport. Les soumissions des analystes sont mises à jour tout au long de la journée.
Analyste Institution David Toung Argus Research Company Ishan Majumdar Baptista Research Charles Butler Barclays
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