Bristol-Myers Squibb Co header image

Bristol-Myers Squibb Co

BMY

Equity

ISIN null / Valor 914188

New York Stock Exchange, Inc (2026-05-22)
USD 59.46-0.15%

Bristol-Myers Squibb Co
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About company

Bristol-Myers Squibb is a global biopharmaceutical company that researches, develops, manufactures and commercializes prescription medicines, with a commercial focus on oncology, hematology, immunology and cardiovascular disease. Its marketed portfolio includes immuno‑oncology therapies such as nivolumab (Opdivo), the widely used anticoagulant apixaban (Eliquis, co‑developed with Pfizer) and a range of treatments for blood cancers and autoimmune conditions, while its pipeline covers targeted small molecules, biologics and emerging modalities including cell therapies. The company generates revenue from global product sales, licensing and collaboration agreements and supports those commercial activities with substantial R&D and clinical development operations; its 2019 acquisition of Celgene significantly expanded its hematology and oncology franchises. Headquartered in New York, Bristol‑Myers Squibb operates worldwide as a publicly traded pharmaceutical firm.

Summarized from source with an LLMView SourceSector: Healthcare

Latest Results (25.04.2026):

Bristol-Myers Squibb Co — fourth quarter of 2025: Total Q4 revenues were $12.5 billion (up 1% year‑over‑year), driven by a 16% increase in the Growth Portfolio to $7.4 billion. Q4 GAAP EPS was $0.53 and non‑GAAP EPS was $1.26 (both include a net impact of $(0.60) from Acquired IPRD charges and licensing income). Full‑year 2025 revenues were $48.2 billion; full‑year GAAP EPS was $3.46 and non‑GAAP EPS was $6.15 (net impact $(1.40)). The company provided 2026 guidance of ~$46.0–$47.5 billion in revenues and non‑GAAP EPS of $6.05–$6.35, and increased the quarterly dividend to $0.63 per share.

Revenue snapshot

Q4 total revenues: $12.502B (+1% reported, roughly flat ex‑FX). Growth Portfolio: $7.393B (+16% reported, +15% ex‑FX). Legacy Portfolio: $5.109B (‑15% reported, ‑16% ex‑FX). Q4 regional mix: U.S. $8.558B; International $3.944B.

Earnings and net income

Q4 GAAP EPS $0.53; Q4 non‑GAAP EPS $1.26 (both include net Acquired IPRD/licensing impact of $(0.60)). Q4 net income attributable to BMS: ~$1.1B GAAP; ~$2.6B non‑GAAP. Full‑year 2025: GAAP EPS $3.46, non‑GAAP EPS $6.15; full‑year net income attributable ~$7.1B GAAP and ~$12.5B non‑GAAP.

Specified items and cost trends

Q4 Acquired IPRD charges were $1.393B (increase vs prior year) driven by the 2025 Orbital Therapeutics acquisition; full‑year Acquired IPRD charges were $3.721B (lower than prior year, which included Karuna). Q4 amortization of acquired intangible assets fell to $826M. GAAP gross margin in Q4 rose to 67.2%; non‑GAAP gross margin was 71.9% (down vs prior year non‑GAAP), reflecting product mix and specified adjustments.

Product performance — key drivers

Growth Portfolio leaders in Q4: Opdivo $2.693B (WW +9%), Breyanzi $392M (WW +49%), Reblozyl $666M (WW +22%), Camzyos $353M (WW +59%). Legacy leader Eliquis: $3.453B Q4 (WW +8%). Growth Portfolio strength offset declines across much of the Legacy portfolio due to expected generic pressure and higher U.S. government channel rebates.

Capital allocation & dividend

Board increased the quarterly common dividend to $0.63 per share (annualized $2.52) — the 17th consecutive annual dividend increase and the 94th consecutive year of dividend payments. Management cites a strengthened balance sheet and continued investment capacity for growth drivers.

2026 guidance highlights

Non‑GAAP guidance: total revenues ~$46.0–$47.5B; non‑GAAP diluted EPS $6.05–$6.35; non‑GAAP gross margin ~69%–70%; operating expenses ~ $16.3B. Company expects Legacy Portfolio to decline ~12–16% in 2026, partially offset by Growth Portfolio. Eliquis WW revenue expected to grow ~10–15% vs. 2025.

Pipeline & business development

Recent milestones: Camzyos Phase 3 SCOUT‑HCM positive in adolescents; FDA priority review for Opdivo supplemental filing in untreated Stage III/IV classical Hodgkin lymphoma (PDUFA goal date Apr 8, 2026); Breyanzi approvals (U.S. for relapsed/refractory marginal zone lymphoma; EU for mantle cell lymphoma); promising pumitamig Phase 2 interim data; discontinuation of the milvexian Librexia ACS trial (no new safety concerns). In Jan 2026 BMS announced a Microsoft collaboration to deploy FDA‑cleared radiology AI to aid early lung cancer detection.

Summarized from source with an LLMView Source

Key figures

26.4%1Y
-9.65%3Y
-11.3%5Y

Performance

27.8%1Y
26.9%3Y
24.0%5Y

Volatility

Market cap

121422 M

Market cap (USD)

Daily traded volume (Shares)

6,489,774

Daily traded volume (Shares)

1 day high/low

57.55 / 56.05

1 day high/low (USD)

52 weeks high/low

0.00 / 0.00

52 weeks high/low (USD)

Dividend ex-date

01 January, 2022

Dividend ex-date

Dividend

0.00

Dividend (USD)

Dividend yield (p.a.)

0.00%

Dividend yield (p.a.)

0.002022
0.002023
0.002024

Est dividend (USD)

0.00%2022
0.00%2023
0.00%2024

Est dividend yield

P/E ratio

10.00

P/E ratio

00.002022
00.002023
00.002024

Est P/E ratio

EPS

0.00

EPS (USD)

0.002022
0.002023
0.002024

Est EPS (USD)

Ratings & reviews

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4.00

2 votes
Performance:
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4.00
Innovation:
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3.00
Society:
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4.00
Nature:
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4.00
Nojus Okleiteris
Netherlands, 09 Nov 2025
star star star star star
.
Markus Dathe
Switzerland, 28 Mar 2025
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Big Pharma.

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