Bristol-Myers Squibb Company

BMY

US1101221083

Bristol-Myers Squibb Company est spécialisé dans le développement, la fabrication et la commercialisation de produits pharmaceutiques. Les produits sont destinés au traitement des cancers, des maladies cardio-vasculaires, de l'hépatite, des maladies immunitaires et des désordres psychiatriques. The United States account for 70.1% of net sales.

Sector

Pharmaceuticals

Calendar

05:30pm - American Society of Clinical Psychopharmacology Meeting - Poster Number: T76

Related indices

S&P 500

More about the company

Income Statement Evolution

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Analysis / Opinion

Christopher Boerner, CEO of Bristol-Myers: A pipeline of 16 treatments, with a focus on neuroscience and oncology

January 09, 2024 at 06:06 pm

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Ratings for Bristol-Myers Squibb Company

Trading Rating

Investor Rating

ESG Refinitiv

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Analysts' Consensus

Sell

Buy

Mean consensus

HOLD

Number of Analysts

Last Close Price

40.25 USD

Average target price

53.19 USD

Spread / Average Target

+32.16%

Consensus

EPS Revisions

Estimates Revisions

Quarterly earnings - Rate of surprise

Company calendar

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Real-time Estimate Cboe BZX Other stock markets 20:36:33 30/05/2024 BST			5-day change	1st Jan Change
40.38 ^USD	+0.31%		-2.86%	-21.36%

06:57pm	Bristol-Myers Squibb Says Breyanzi Gets FDA Approval as CAR T Cell Therapy for Mantle Cell Lymphoma	MT
06:22pm	Bristol Myers: FDA approval for Breyanzi	CF

Bristol-Myers Squibb Says Breyanzi Gets FDA Approval as CAR T Cell Therapy for Mantle Cell Lymphoma	05:57pm	MT
Bristol Myers: FDA approval for Breyanzi	05:22pm	CF
US FDA allows use of Bristol's cell therapy for rare blood cancer	04:55pm	RE
Bristol Myers Squibb’s Urothelial Carcinoma Combo Drug Gets EU Commission Approval	05-29	MT
Bristol-Myers Squibb Gains EU Approval for Opdivo Combination Therapy for Urothelial Cancer	05-29	MT
Bristol Myers: new EC approval for Opdivo	05-29	CF
Bristol Myers Squibb Receives European Commission Approval for Opdivo in Combination with Cisplatin and Gemcitabine	05-29	CI
Prothena to Receive $80 Million From Bristol-Myers Squibb For PRX019 Global License	05-28	MT
Bristol Myers: will present data on schizophrenia	05-27	CF
Bristol Myers: presents over 130 studies at ASCO	05-27	CF
Bristol-Myers Squibb Unveils Positive Data for KarXT in Schizophrenia Treatment	05-23	MT
Bristol Myers, Sanofi liability in Hawaii Plavix case grows to $916 million	05-22	RE
Bristol-Myers Squibb Announces Strategies to Improve Access to Medicines	05-22	MT
Bristol Myers: 10-year strategy for poor countries	05-22	CF
Bristol-Myers Squibb Invests in NeoPhore	05-22	MT
Neophore Limited announced that it has received funding from a group of investors	05-21	CI
Bristol Myers: national schizophrenia campaign	05-21	CF
Bristol-Myers Squibb Says US FDA Reassigns Action Date Subcutaneous Nivolumab	05-21	MT
Bristol Myers: deadline set for subcutaneous Opdivo	05-21	CF
Bristol Myers Squibb Announces Updated Action Date by the U.S. Food and Drug Administration for Subcutaneous Nivolumab (Nivolumab and Hyaluronidase)	05-21	CI
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	05-16	CI
Everlasting momentum	05-16
Bristol Myers Gets FDA OK of Breyanzi in Follicular Lymphoma	05-16	DJ
Bristol-Myers Squibb Gets FDA Accelerated Approval for Breyanzi for Follicular Lymphoma	05-16	MT
Bristol Myers Squibb's CAR T Cell Therapy Breyanzi Approves by the U.S. Food and Drug Administration for Relapsed or Refractory Follicular Lymphoma	05-16	CI