BMYB34 Stoklara Genel Bakış Bristol-Myers Squibb Company biyofarmasötik ürünleri keşfeder, geliştirir, lisanslar, üretir, pazarlar, dağıtır ve dünya çapında satar. Daha fazla detay
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Bristol-Myers Squibb Company Rakipler Fiyat Geçmişi ve Performans
Hisse fiyatlarındaki yükseliş, düşüş ve değişimlerin özeti Bristol-Myers Squibb Tarihsel hisse senedi fiyatları Güncel Hisse Fiyatı US$347.97 52 Haftanın En Yüksek Seviyesi US$363.51 52 Haftanın En Düşük Seviyesi US$203.10 Beta 0.45 1 Aylık Değişim -2.91% 3 Aylık Değişim 8.27% 1 Yıllık Değişim 46.14% 3 Yıllık Değişim 1.94% 5 Yıllık Değişim 20.70% Halka arzdan bu yana değişim 428.19%
Son Haberler & Güncellemeler Bristol Myers Squibb Receives Positive Chmp Opinion for Car T Cell Therapy Breyanzi for Relapsed or Refractory Follicular Lymphoma
Bristol Myers Squibb Presents Results from Checkmate -8Hw Analysis Evaluating Opdivo® (Nivolumab) Plus Yervoy® (Ipilimumab) Compared to Opdivo Monotherap Jan 27
Bristol Myers Squibb Announces FDA Approval of Cobenfy Jan 08
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 Daha fazla güncelleme görün Bristol Myers Squibb Receives Positive Chmp Opinion for Car T Cell Therapy Breyanzi for Relapsed or Refractory Follicular Lymphoma
Bristol Myers Squibb Presents Results from Checkmate -8Hw Analysis Evaluating Opdivo® (Nivolumab) Plus Yervoy® (Ipilimumab) Compared to Opdivo Monotherap Jan 27
Bristol Myers Squibb Announces FDA Approval of Cobenfy Jan 08
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 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
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
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
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
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
Bristol-Myers Squibb Company (NYSE:BMY) entered into definitive merger agreement to acquire RayzeBio, Inc. (NasdaqGM:RYZB) for $3.8 billion. Dec 27 Hissedar Getirileri BMYB34 BR Pharmaceuticals BR Pazar 7D -3.3% 0.4% 0.9% 1Y 46.1% -16.4% -7.2%
Hissedar getirilerinin tamamını görün
Getiri vs. Endüstri: BMYB34 geçen yıl % -16.4 oranında getiri sağlayan BR Pharmaceuticals sektörünü aştı.
Getiri vs Piyasa: BMYB34 geçen yıl % -7.2 oranında getiri sağlayan BR Piyasasını aştı.
Fiyat Oynaklığı Is BMYB34's price volatile compared to industry and market? BMYB34 volatility BMYB34 Average Weekly Movement 6.9% Pharmaceuticals Industry Average Movement 5.8% Market Average Movement 5.6% 10% most volatile stocks in BR Market 10.0% 10% least volatile stocks in BR Market 3.2%
İstikrarlı Hisse Senedi Fiyatı: BMYB34 son 3 ayda BR piyasasına kıyasla önemli bir fiyat oynaklığı yaşamadı.
Zaman İçindeki Volatilite: BMYB34 'nin haftalık oynaklığı ( 7% ) son bir yıldır istikrarlı seyretti.
Şirket Hakkında Kuruldu Çalışanlar CEO Web sitesi 1887 34,100 Chris Boerner www.bms.com
Bristol-Myers Squibb Company dünya çapında biyofarmasötik ürünler keşfeder, geliştirir, lisanslar, üretir, pazarlar, dağıtır ve satar. Hematoloji, onkoloji, kardiyovasküler, immünoloji, fibrotik ve nörobilim hastalıkları için ürünler sunmaktadır. Şirketin ürünleri arasında valvüler olmayan atriyal fibrilasyonda inme/sistemik emboli riskini azaltmak ve DVT/PE tedavisi için Eliquis; mesane, kan, CRC, baş ve boyun, RCC, HCC, akciğer, melanom, MPM, mide ve özofagus kanseri dahil olmak üzere çeşitli anti-kanser endikasyonları için Opdivo bulunmaktadır; Multipl miyelom için Pomalyst/Imnovid; aktif romatoid artrit ve psoriatik artrit için Orencia; ve Philadelphia kromozomu pozitif kronik miyeloid lösemi tedavisi için Sprycel.
Daha fazla göster Bristol-Myers Squibb Company Temel Bilgiler Özeti Bristol-Myers Squibb'un kazançları ve gelirleri piyasa değeriyle nasıl karşılaştırılır? BMYB34 temel i̇stati̇sti̇kler Piyasa değeri R$694.70b Kazançlar(TTM ) -R$42.17b Gelir(TTM ) R$275.62b
Kazanç ve Gelir En son kazanç raporundan temel karlılık istatistikleri (TTM) BMYB34 gelir tablosu (TTM ) Gelir US$47.44b Gelir Maliyeti US$11.44b Brüt Kâr US$35.99b Diğer Giderler US$43.25b Kazançlar -US$7.26b
Son Raporlanan Kazançlar
Sep 30, 2024
Sonraki Kazanç Tarihi
Feb 06, 2025
Hisse başına kazanç (EPS) -3.58 Brüt Marj 75.87% Net Kâr Marjı -15.30% Borç/Özkaynak Oranı 289.5%
BMYB34 uzun vadede nasıl bir performans gösterdi?
Geçmiş performansı ve karşılaştırmayı görün Temettüler
4.1% Mevcut Temettü Verimi Yaklaşan bir temettüyü almak için ne zaman BMYB34 satın almanız gerekir? Bristol-Myers Squibb temettü tari̇hleri̇ Eski Temettü Tarihi Jan 02 2025 Temettü Ödeme Tarihi Feb 12 2025 Eski temettüye kadar geçen günler 34 days Temettü ödeme tarihine kadar geçen günler 7 days
Şirket Analizi ve Finansal Veri Durumu Veri Son Güncelleme (UTC saati) Şirket Analizi 2025/02/03 17:39 Gün Sonu Hisse Fiyatı 2025/02/03 00:00 Kazançlar 2024/09/30 Yıllık Kazançlar 2023/12/31
Veri Kaynakları Şirket analizimizde kullanılan veriler S&P Global Market Intelligence LLC 'den alınmıştır. Bu raporu oluşturmak için analiz modelimizde aşağıdaki veriler kullanılmıştır. Veriler normalize edilmiştir, bu da kaynağın mevcut olmasından kaynaklanan bir gecikmeye neden olabilir.
Paket Veri Zaman Çerçevesi Örnek ABD Kaynağı * Şirket Finansalları 10 yıl Gelir tablosu Nakit akış tablosu Bilanço Analist Konsensüs Tahminleri +3 yıl Finansal tahminler Analist fiyat hedefleri Piyasa Fiyatları 30 yıl Hisse senedi fiyatları Temettüler, Bölünmeler ve Eylemler Sahiplik 10 yıl En büyük hissedarlar İçeriden öğrenenlerin ticareti Yönetim 10 yıl Liderlik ekibi Yönetim Kurulu Önemli Gelişmeler 10 yıl
* ABD menkul kıymetleri için örnek, ABD dışı için eşdeğer düzenleyici formlar ve kaynaklar kullanılır.
Belirtilmediği sürece tüm finansal veriler yıllık bir döneme dayanmaktadır ancak üç ayda bir güncellenmektedir. Bu, İzleyen On İki Ay (TTM) veya Son On İki Ay (LTM) Verileri olarak bilinir. Buradan daha fazla bilgi edinin.
Analiz Modeli ve Kar Tanesi Bu raporu oluşturmak için kullanılan analiz modelinin ayrıntıları Github sayfamızda mevcuttur, ayrıca raporlarımızın nasıl kullanılacağına dair kılavuzlarımız ve Youtube' da eğitimlerimiz bulunmaktadır.
Simply Wall St analiz modelini tasarlayan ve oluşturan dünya standartlarındaki ekip hakkında bilgi edinin.
Endüstri ve Sektör Metrikleri Sektör ve bölüm metriklerimiz Simply Wall St tarafından her 6 saatte bir hesaplanmaktadır, sürecimizin ayrıntıları 'da mevcuttur.
Analist Kaynakları Bristol-Myers Squibb Company 50 Bu analistlerden 25, raporumuzun girdisi olarak kullanılan gelir veya kazanç tahminlerini sunmuştur. Analistlerin gönderimleri gün boyunca güncellenmektedir.
Analist Kurum David Toung Argus Research Company Ishan Majumdar Baptista Research Charles Butler Barclays
Göster 47 daha fazla analist 
