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Previsão
O preço-alvo médio dos analistas é € 58,80 (+7,69%). A mediana é € 57,84 (+5,93%).
| Comprar |
19 |
| Manter |
21 |
| Vender |
2 |
Notícias Ir para o feed de notícias
Bristol Myers Squibb: Phase-3 data on RYZ101 confirm expansion of precision oncology
The drug RYZ101 met the primary endpoint in a Phase-3 study and improved progression-free survival, supporting the focus on precision oncology. Bristol Myers Squibb sees the results as validation of its strategy to generate additional growth through acquisitions. The company is in a consolidation phase and expects 2026 revenue of $49–50 billion while aiming to offset revenue losses from expiring patents. » Mais em finanzen.net
Bristol-Myers Squibb reaches 52-week high at $68.10
Bristol-Myers Squibb shares rose to a 52-week high of $68.10 and have gained about 43% over the past year. The stock trades at a P/E ratio of 14.6 but is rated by InvestingPro as overvalued relative to fair value; the company has paid a dividend for 56 years, with a yield of 3.82%. Additionally, the company reported an accelerated approval for Zenbexus, Guggenheim confirmed a "Buy" with a $75.00 target, and Bristol-Myers plans an approximately $2.3 billion production facility in Houston; market rumours of possible takeover interest from AstraZeneca remain unconfirmed. » Mais em de.investing.com
FDA accelerates approval for Bristol Myers Squibb drug Zenbexus for multiple myeloma
The FDA granted Bristol Myers Squibb accelerated approval for Zenbexus (iberdomid) in combination with daratumumab (with hyaluronidase) and dexamethasone for the treatment of adult patients with multiple myeloma after at least one prior therapy. Zenbexus is the first approved cereblon‑modulating protein degrader; the decision is based on the Phase 3 EXCALIBER‑RRMM study, in which 41% of patients treated with the combination achieved a complete remission without minimal residual disease versus 21% in the control arm (median follow‑up 16 months). The approval is conditional on confirmatory trials that will evaluate, among other endpoints, progression‑free survival. Key safety information includes embryofetal toxicity, thromboembolic risks, a REMS program, a high rate of serious adverse events (58.3%) and pronounced neutropenia (90.2%); 4.9% of patients experienced fatal adverse events. Bristol Myers Squibb is also developing mezigdomid, with an FDA decision targeted for May 13, 2027. » Mais em de.investing.com
Dividendos históricos Dividendos
Todos os indicadores de dividendos Todos os indicadoresDados financeiros da empresa
| (EUR) | junho de 2026 | YoY |
|---|---|---|
| Receitas | 11,37 bi | 9,20% |
| Ganho bruto | 8,1 bi | 7,34% |
| Ganho líquido | 2,91 bi | 161,50% |
| EBITDA | 4,46 bi | 60,71% |
Dados fundamentais
| Métrica | Valor |
|---|---|
Capitalização bolsista | € 107,61 bi |
Número de ações | 2,04 bi |
Máximo/mínimo de 52 semanas | € 61,07 - € 37,83 |
Rentabilidade de dividendos | 3,97% |
Dividendos TTM | € 2,16 |
Próximo dividendo | € 0,56 |
Beta | 0,23 |
PER (PE Ratio) | 13,04 |
PEG (PEG Ratio) | 0,16 |
P/VC (PB Ratio) | 5,42 |
P/V (PS Ratio) | 2,46 |
Perfil da empresa
Bristol-Myers Squibb Company erforscht, entwickelt, lizenziert, produziert und vermarktet weltweit biopharmazeutische Produkte. Das Unternehmen bietet Produkte für die Bereiche Hämatologie, Onkologie, Herz-Kreislauf, Immunologie, Fibrosen, Neurowissenschaften und Covid-19-Erkrankungen an. Zu den Produkten des Unternehmens gehören Revlimid, ein orales immunmodulatorisches Medikament zur Behandlung des multiplen Myeloms; Eliquis, ein oraler Inhibitor zur Verringerung des Risikos eines Schlaganfalls/einer systemischen Embolie bei NVAF und zur Behandlung von TVT/PE; Opdivo für Krebsindikationen; Pomalyst/Imnovid für Patienten mit multiplem Myelom; und Orencia für erwachsene Patienten mit aktiver RA und Psoriasis-Arthritis. Darüber hinaus bietet das Unternehmen Sprycel zur Behandlung von Philadelphia-Chromosom-positiver chronisch-myeloischer Leukämie, Yervoy zur Behandlung von Patienten mit inoperablem oder metastasiertem Melanom, Abraxane, ein proteingebundenes Chemotherapieprodukt, Reblozyl zur Behandlung von Anämie bei erwachsenen Patienten mit Beta-Thalassämie und Empliciti zur Behandlung des multiplen Myeloms. Darüber hinaus bietet das Unternehmen Zeposia zur Behandlung rezidivierender Formen der Multiplen Sklerose, Breyanzi, eine CD19-gerichtete, genetisch modifizierte autologe T-Zell-Immuntherapie zur Behandlung erwachsener Patienten mit rezidivierendem oder refraktärem großzelligem B-Zell-Lymphom, Inrebic, einen oralen Kinaseinhibitor zur Behandlung erwachsener Patienten mit Myelofibrose, und Onureg zur Behandlung erwachsener Patienten mit AML an. Das Unternehmen vertreibt seine Produkte an Großhändler, Distributoren, Apotheken, Einzelhändler, Krankenhäuser, Kliniken und Behörden. Das Unternehmen war früher unter dem Namen Bristol-Myers Company bekannt. Das Unternehmen wurde 1887 gegründet und hat seinen Hauptsitz in New York, New York.
| Nome | Bristol Myers Squibb |
| CEO | Christopher Boerner |
| Sede | Princeton,
nj EUA |
| Site | |
| Setor | Cuidados de saúde |
| Indústria | Produtos farmacêuticos |
| Entrada em bolsa | 01/06/1972 |
| Colaboradores | 32.500 |
Análise aprofundada
Símbolos de ticker
| Bolsa | Símbolo |
|---|---|
NASDAQ | |
NYSE | BMY |
XETRA | BRM.DE |
Düsseldorf | BRM.DU |
Frankfurt | BRM.F |
Hamburg | BRM.HM |
London | 0R1F.L |
München | BRM.MU |
SIX | BMYUSD.SW |
Wien | BMYS.VI |
Milan | 1BMY.MI |
Bse | QUEST.BO |
Sao | KEPL3.SA |
Pnk | ERFB |
London Stock Exchange | 0RP6.L |