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850501
BMY

Bristol Myers Squibb

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  • 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. » Mere på 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. » Mere på 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. » Mere på de.investing.com


  • Bristol-Myers Squibb said to be negotiating a merger with Astrazeneca

    According to reports, Bristol-Myers Squibb is negotiating a possible merger with Astrazeneca. The stock gave up early gains and closed 0.2 percent higher. Analysts voiced criticism, pointing in particular to substantial antitrust hurdles for such a mega-merger. » Mere på finanzen.net


  • Merger speculation with Bristol Myers Squibb weighs on AstraZeneca stock

    AstraZeneca shares fell about 8.7% in morning trading to $154.88 after reports of initial merger talks with Bristol Myers Squibb, a possible tie-up with a combined valuation of nearly $400 billion. Analysts flagged regulatory hurdles, possible takeover premiums and dilution risks that could further weigh on the stock. It is unclear whether talks will continue or result in a transaction, adding further uncertainty. Meanwhile, Bristol Myers Squibb shares rose as a potential takeover target, while the broader US market remained resilient. » Mere på de.investing.com

I 2026 har Bristol Myers Squibb allerede udloddet 2,18 € i udbytte. Den seneste udlodning fandt sted i november.

Virksomhedstal

I det seneste kvartal havde Bristol Myers Squibb en omsætning på 11,54 mia. € og et nettoresultat på 1,91 mia. €
(EUR) september 2026
YoY
Omsætning 11,54 mia. 10,79 %
Bruttofortjeneste 7,88 mia. 5,21 %
Nettoresultat 1,91 mia. 1,77 %
EBITDA 2,59 mia. 33,88 %

Fundamentale data

Nøgletal Værdi
Markedsværdi
115,51 mia. €
Antal aktier
2,04 mia.
Højeste/laveste i 52 uger
61,96 € - 40,86 €
Udbytteafkast
3,85 %
Udbytte TTM
2,18 €
Beta
0,23
P/E (PE Ratio)
13,85
PEG (PEG Ratio)
0,27
K/I (PB Ratio)
5,46
P/S (PS Ratio)
2,56

Virksomhedsprofil

Bristol-Myers Squibb Company opdager, udvikler, licenserer, fremstiller og markedsfører biofarmaceutiske produkter over hele verden. Virksomheden tilbyder produkter til behandling af sygdomme inden for hæmatologi, onkologi, kardiovaskulær sygdom, immunologi, fibrotiske sygdomme, neurovidenskab og covid-19. Virksomhedens produkter omfatter Revlimid, et oralt immunmodulerende lægemiddel til behandling af multipel myelom; Eliquis, en oral hæmmer til reduktion af risikoen for slagtilfælde og systemisk embolisme ved NVAF samt til behandling af DVT/PE; Opdivo til anti-kræftindikationer; Pomalyst/Imnovid, indiceret til patienter med multipel myelom; og Orencia til voksne patienter med aktiv RA og psoriasisartrit. Virksomheden leverer også Sprycel til behandling af Philadelphia-kromosompositiv kronisk myeloid leukæmi; Yervoy til behandling af patienter med ikke-resektabelt eller metastatisk melanom; Abraxane, et proteinbundet kemoterapipræparat; Reblozyl til behandling af anæmi hos voksne patienter med beta-thalassæmi; og Empliciti til behandling af multipel myelom. Derudover tilbyder virksomheden Zeposia til behandling af recidiverende former for multipel sclerose; Breyanzi, en CD19-rettet, genetisk modificeret autolog T-celleimmunterapi til behandling af voksne patienter med recidiverende eller refraktært storcellet B-cellelymfom; Inrebic, en oral kinasehæmmer indiceret til behandling af voksne patienter med myelofibrose; og Onureg til behandling af voksne patienter med AML. Virksomheden sælger produkter til grossister, distributører, apoteker, detailhandlere, hospitaler, klinikker og statslige myndigheder. Virksomheden var tidligere kendt som Bristol-Myers Company. Virksomheden blev grundlagt i 1887 og har hovedkontor i New York, New York.

Navn
Bristol Myers Squibb
CEO
Christopher Boerner
Hjemsted Princeton, nj
USA
Websted
Sektor
Sundhed
Branche
Lægemidler
Børsnotering
01.06.1972
Medarbejdere 32.500

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