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Forecast
The analysts' average price target is €59.13 (+7.43%). The median is €58.16 (+5.67%).
| Buy |
19 |
| Hold |
21 |
| Sell |
2 |
News Go to news feed
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. » More on 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. » More on 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. » More on de.investing.com
Historical dividends Dividends
All dividend metrics All metricsFinancials
| (EUR) | June 2026 | YoY |
|---|---|---|
| Revenue | 11.37B | 9.20% |
| Gross profit | 8.1B | 7.34% |
| Net profit | 2.91B | 161.50% |
| EBITDA | 4.46B | 60.71% |
Fundamentals
| Metric | Value |
|---|---|
Market capitalization | €112.37B |
Number of shares | 2.04B |
52-week high/low | €61.42 - €38.05 |
Dividend yield | 3.90% |
Dividends TTM | €2.16 |
Next dividend | €0.56 |
Beta | 0.23 |
P/E ratio | 13.54 |
PEG ratio | 0.16 |
P/B ratio | 5.62 |
P/S ratio | 2.55 |
Company profile
Bristol-Myers Squibb Company discovers, develops, licenses, manufactures, and markets biopharmaceutical products worldwide. It offers products for hematology, oncology, cardiovascular, immunology, fibrotic, neuroscience, and covid-19 diseases. The company's products include Revlimid, an oral immunomodulatory drug for the treatment of multiple myeloma; Eliquis, an oral inhibitor for reduction in risk of stroke/systemic embolism in NVAF, and for the treatment of DVT/PE; Opdivo for anti-cancer indications; Pomalyst/Imnovid indicated for patients with multiple myeloma; and Orencia for adult patients with active RA and psoriatic arthritis. It also provides Sprycel for the treatment of Philadelphia chromosome-positive chronic myeloid leukemia; Yervoy for the treatment of patients with unresectable or metastatic melanoma; Abraxane, a protein-bound chemotherapy product; Reblozyl for the treatment of anemia in adult patients with beta thalassemia; and Empliciti for the treatment of multiple myeloma. In addition, the company offers Zeposia to treat relapsing forms of multiple sclerosis; Breyanzi, a CD19-directed genetically modified autologous T cell immunotherapy for the treatment of adult patients with relapsed or refractory large B-cell lymphoma; Inrebic, an oral kinase inhibitor indicated for the treatment of adult patients with myelofibrosis; and Onureg for the treatment of adult patients with AML. It sells products to wholesalers, distributors, pharmacies, retailers, hospitals, clinics, and government agencies. The company was formerly known as Bristol-Myers Company. The company was founded in 1887 and is headquartered in New York, New York.
| Name | Bristol Myers Squibb |
| CEO | Christopher Boerner |
| Headquarters | Princeton,
nj USA |
| Website | |
| Sector | Health Care |
| Industry | Pharmaceuticals |
| IPO | 06/01/1972 |
| Employees | 32,500 |
Ticker symbols
| Exchange | Symbol |
|---|---|
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 |