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BMY

Bristol Myers Squibb (BMY)

Bristol Myers Squibb Co
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DatumZeitQuelleÜberschriftSymbolFirma
01/05/202414h00GlobeNewswire Inc.Editas Medicine and Bristol Myers Squibb Extend Alpha-Beta T Cell CollaborationNYSE:BMYBristol Myers Squibb Co
29/04/202412h00PR Newswire (US)Repertoire® Immune Medicines and Bristol Myers Squibb Announce Multi-Year Strategic Collaboration to Develop Tolerizing Vaccines for Autoimmune DiseasesNYSE:BMYBristol Myers Squibb Co
26/04/202412h59Business WireCHMP 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 CarcinomaNYSE:BMYBristol Myers Squibb Co
25/04/202413h53IH Market NewsU.S. Futures Drop in Pre-Market Trading as Tech Stocks Plunge After Meta Issues Gloomy ForecastNYSE:BMYBristol Myers Squibb Co
25/04/202412h59Business WireBristol Myers Squibb Reports First Quarter Financial Results for 2024NYSE:BMYBristol Myers Squibb Co
23/04/202413h25IH Market NewsApple Loses Market Share in China, GM Surges in Pre-Market Following Upward Revisions for 2024 Projections, and More NewsNYSE:BMYBristol Myers Squibb Co
22/04/202412h59Business WireBristol Myers Squibb and Cellares Announce a $380M Worldwide Capacity Reservation and Supply Agreement for the Manufacture of CAR T Cell Therapies to Bring the Promise of Cell Therapy to More Patients, FasterNYSE:BMYBristol Myers Squibb Co
22/04/202412h59Business WireBristol Myers Squibb and Cellares Announce a $380M Worldwide Capacity Reservation and Supply Agreement for the Manufacture of CAR T Cell Therapies to Bring the Promise of Cell Therapy to More Patients, FasterNYSE:BMYBristol Myers Squibb Co
08/04/202417h30Business WireKRAZATI (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)NYSE:BMYBristol Myers Squibb Co
06/04/202419h15Business Wire Bristol Myers Squibb Presents New Pooled Interim Long-Term Safety and Metabolic Outcomes Data from the EMERGENT Program Evaluating KarXT in Schizophrenia at the 2024 Annual Congress of the Schizophrenia International Research SocietyNYSE:BMYBristol Myers Squibb Co
06/04/202419h15Business WireBristol Myers Squibb Presents New Interim Long-Term Efficacy Data from the EMERGENT-4 Trial Evaluating KarXT in Schizophrenia at the 2024 Annual Congress of the Schizophrenia International Research SocietyNYSE:BMYBristol Myers Squibb Co
05/04/202415h05Business WireU.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 TherapyNYSE:BMYBristol Myers Squibb Co
03/04/202402h08Business WireEuropean Commission Expands Approval of Bristol Myers Squibb’s Reblozyl® (luspatercept) to Include First-Line Treatment of Transfusion-Dependent Anemia in Adults with Lower-Risk Myelodysplastic Syndromes (LR-MDS)NYSE:BMYBristol Myers Squibb Co
02/04/202412h59Business WireBristol Myers Squibb Releases 2023 Environmental, Social and Governance Report Demonstrating Progress and Setting New Long-Term GoalsNYSE:BMYBristol Myers Squibb Co
28/03/202421h05Business WireBristol Myers Squibb Announces Pivotal KRYSTAL-12 Confirmatory Trial Evaluating KRAZATI (adagrasib) Meets Primary Endpoint of Progression-Free Survival for Patients with Pretreated KRASG12C-Mutated Locally Advanced or Metastatic Non-Small Cell Lung…NYSE:BMYBristol Myers Squibb Co
28/03/202421h01Business WireBristol Myers Squibb Provides Update on the First Phase 3 YELLOWSTONE Trial Evaluating Oral Zeposia (ozanimod) in Patients with Moderate to Severe Active Crohn’s DiseaseNYSE:BMYBristol Myers Squibb Co
28/03/202412h30GlobeNewswire Inc.Perspective Therapeutics Provides Recent Business Highlights and Reports Fiscal Year 2023 Financial ResultsNYSE:BMYBristol Myers Squibb Co
26/03/202419h25Business WireA Bristol Myers Squibb Expande as Iniciativas de Doações para a Equidade em Saúde a fim de Melhorar os Resultados de SaúdeNYSE:BMYBristol Myers Squibb Co
26/03/202411h59Business WireBristol Myers Squibb Expands Health Equity Grant Initiatives to Improve Health OutcomesNYSE:BMYBristol Myers Squibb Co
25/03/202413h00Business WireBristol Myers Squibb to Present Data at the American College of Cardiology Annual Scientific Session 2024 Reinforcing Extensive Body of Evidence in Clinical and Real-World Settings Across Cardiovascular PortfolioNYSE:BMYBristol Myers Squibb Co
20/03/202421h45Business WireBristol 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 MyelomaNYSE:BMYBristol Myers Squibb Co
20/03/202411h59Business WireBristol Myers Squibb Announces CheckMate -9DW Trial Evaluating Opdivo (nivolumab) Plus Yervoy (ipilimumab) Meets Primary Endpoint of Overall Survival for the First-Line Treatment of Advanced Hepatocellular CarcinomaNYSE:BMYBristol Myers Squibb Co
19/03/202411h59Business WireBristol Myers Squibb and Ted Danson Empower Those with Plaque Psoriasis to Take Action in “SO, Have You Found It?” CampaignNYSE:BMYBristol Myers Squibb Co
18/03/202413h44Business WireBristol Myers Squibb Completes Acquisition of Karuna Therapeutics, Strengthening Neuroscience PortfolioNYSE:BMYBristol Myers Squibb Co
15/03/202423h27Business WireFDA Advisory Committee Votes in Favor of Bristol Myers Squibb’s and 2seventy bio’s Abecma for Triple-Class Exposed Multiple Myeloma in Earlier Lines of TherapyNYSE:BMYBristol Myers Squibb Co
15/03/202402h35Business WireU.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 (CLL) or Small Lymphocytic Lymphoma (SLL)NYSE:BMYBristol Myers Squibb Co
11/03/202421h16Business WireBristol Myers Squibb to Report Results for First Quarter 2024 on April 25, 2024NYSE:BMYBristol Myers Squibb Co
07/03/202420h23Business WireU.S. Food and Drug Administration Approves Opdivo® (nivolumab), in Combination with Cisplatin and Gemcitabine, for First-Line Treatment of Adult Patients with Unresectable or Metastatic Urothelial CarcinomaNYSE:BMYBristol Myers Squibb Co
06/03/202422h17Business WireBristol Myers Squibb to Participate in Upcoming Investor ConferencesNYSE:BMYBristol Myers Squibb Co
04/03/202423h57Edgar (US Regulatory)Form 4 - Statement of changes in beneficial ownership of securitiesNYSE:BMYBristol Myers Squibb Co
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