BMY on NYSE

Bristol-Myers Squibb

Logo: Bristol-Myers Squibb, Public domain, via Wikimedia Commons6

American pharmaceutical company

Bristol-Myers Squibb Company, doing business as Bristol Myers Squibb, is an American multinational pharmaceutical company headquartered in Princeton, New Jersey.3 Its chief executive is Giovanni Caforio (since 2015).1 It employed about 30,000 people in 2019.1 Its revenue was $46.2 billion in 2022.1 Its shares trade on NYSE under the symbol BMY.1 Wikipedia text CC BY-SA 4.0

$59.67 down 0.90 (1.48%)Price as of Oct 16, 2026 at 19:58 UTC

Last updated Oct 21, 2026.

Overview

1989Founded1

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  • TickerBMY on NYSE1
  • Industrypharmaceutical industry1
  • HeadquartersNew York City1
  • Founded inClinton1
  • Websitewww.bms.com
  • Legal formDelaware corporation1
  • Incorporated inDE7
  • Business addressRoute 206 And Province Line Road, Princeton, Nj 085437
  • Filer categoryLarge accelerated filer7
  • LEIHLYYNH7UQUORYSJQCN424
  • StatusActive4
  • LEI statusIssued and current4
  • Registered addressC/O THE CORPORATION TRUST COMPANY, 19801 Wilmington, United States4
  • Registered withDivision of Corporations, Department of State, 3265014
Bristolmyersprincetonfacility
Photo: Coolcaesar at English Wikipedia, CC BY-SA 3.0, via Wikimedia Commons13

Bristol-Myers Squibb Company, doing business as Bristol Myers Squibb, is an American multinational pharmaceutical company headquartered in Princeton, New Jersey. The company's primary products are apixaban (Eliquis) for people with atrial fibrillation (30% of 2025 revenues); nivolumab (Opdivo), used to treat certain types of cancer (21% of 2025 revenues); lenalidomide (Revlimid), used to treat multiple myeloma, smoldering myeloma, and myelodysplastic syndromes (6% of 2025 revenues); abatacept (Orencia), used to treat autoimmune diseases such as rheumatoid arthritis (8% of 2025 revenues); pomalidomide (Pomalyst/Imnovid), an anti-cancer medication used for the treatment of multiple myeloma and AIDS-related Kaposi sarcoma (6% of 2025 revenues); ipilimumab (Yervoy), to treat cancer (6% of 2025 revenues); and luspatercept (Reblozyl) for the treatment of anemia in beta thalassemia and myelodysplastic syndromes (5% of 2025 revenues). In 2025, 69% of the company's revenues came from the United States.3

Financials

From the company’s reports to the SEC. Every number links to the filing it came from.

Key numbers, fiscal 2025

14.6%Net margin14
-0.2%Revenue growth, 202514
38.2%Return on equity14
2.32×Debt to equity14
$12.8BFree cash flow14

What sells

Revenue by product, business segment and region, as the company reports it to the SEC.

Products and services

Opdivo brought in 31% of the revenue Bristol-Myers Squibb broke down this way in fiscal 2025.

  1. Opdivo$10.0B1431%up 8% from 2024
  2. Orencia$3.7B1411%up 1% from 2024
  3. Revlimid$3.0B149%down 49% from 2024
  4. Yervoy$2.9B149%up 15% from 2024
  5. Pomalyst/Imnovid$2.7B148%down 23% from 2024
  6. Reblozyl$2.3B147%up 31% from 2024
  7. Other Growth Brands$1.9B146%up 17% from 2024
  8. Alliance And Other Revenues$1.4B144%down 6% from 2024
  9. Breyanzi$1.4B144%up 82% from 2024
  10. Opdualag$1.2B144%up 28% from 2024
  11. Camzyos$1.1B143%up 77% from 2024
  12. Other revenues$992.0M143%down 5% from 2024
Products and services by year
Products and services202320242025
Opdivo$9.0B$9.3B$10.0B
Orencia$3.6B$3.7B$3.7B
Revlimid$6.1B$5.8B$3.0B
Yervoy$2.2B$2.5B$2.9B
Pomalyst/Imnovid$3.4B$3.5B$2.7B
Reblozyl$1.0B$1.8B$2.3B
Other Growth Brands$1.2B$1.6B$1.9B
Alliance And Other Revenues$1.2B$1.5B$1.4B
Breyanzi$364.0M$747.0M$1.4B
Opdualag$627.0M$928.0M$1.2B
Camzyos$231.0M$602.0M$1.1B
Other revenues$620.0M$1.0B$992.0M

Regions

United States brought in 69% of the revenue Bristol-Myers Squibb broke down this way in fiscal 2025.

  1. United States$33.3B1469%down 2% from 2024
  2. Rest of the world$13.8B1429%up 5% from 2024
  3. Other Region$1.1B142%up 9% from 2024
Regions by year
Regions202320242025
United States$31.2B$34.1B$33.3B
Rest of the world$13.1B$13.2B$13.8B
Other Region$699.0M$996.0M$1.1B

Where the money goes

Where each dollar of revenue went, fiscal 2025

  • Cost of revenue29¢$13.9B
  • Research and development21¢$10.0B
  • Selling, general and admin15¢$7.3B
  • Other costs16¢$7.7B
  • Income tax5¢$2.3B
  • Profit15¢$7.1B

Out of $48.2B in revenue.14

Where each dollar of operating cash went, fiscal 2025

  • Capital spending9¢$1.3B
  • Dividends paid36¢$5.0B
  • Kept or used elsewhere55¢$7.8B

Out of $14.2B of cash from operations.14

Financial statements

Revenue1516171814$48.2B in 2025+84% since 2019
0$20.0B$40.0B$60.0B2019: $26.1B$26.1B20192020: $42.5B$42.5B2020+63%2021: $46.4B$46.4B2021+9%2022: $46.2B$46.2B2022−0%2023: $45.0B$45.0B2023−2%2024: $48.3B$48.3B2024+7%2025: $48.2B$48.2B2025−0%
Gross profit19$30.7B in 2020+70% since 2019
0$10.0B$20.0B$30.0B$40.0B2019: $18.1B$18.1B20192020: $30.7B$30.7B2020+70%
Net income1516171814$7.1B in 2025+105% since 2019
-$10.0B-$5.0B0$5.0B$10.0B2019: $3.4B$3.4B20192020: -$9.0B-$9.0B20202021: $7.0B$7.0B20212022: $6.3B$6.3B2022−10%2023: $8.0B$8.0B2023+27%2024: -$8.9B-$8.9B20242025: $7.1B$7.1B2025

Every line of the income statement as filed: the last 3 fiscal years, latest first.14

Period ending2025-12-312024-12-312023-12-31
Total Revenues$48.2B$48.3B$45.0B
Cost of products sold$13.9B$14.0B$10.7B
Selling, general and administrative$7.3B$8.4B$7.8B
Research and development$10.0B$11.2B$9.3B
Acquired IPRD$3.7B$13.4B$913.0M
Amortization of acquired intangible assets$3.3B$8.9B$9.0B
Other (income)/expense, net$674.0M$893.0M-$1.2B
Total Expenses$38.9B$56.7B$36.6B
Earnings/(Loss) before income taxes$9.3B-$8.4B$8.4B
Income tax provision$2.3B$554.0M$400.0M
Net earnings/(loss)$7.1B-$8.9B$8.0B
Noncontrolling Interest$2.0M$15.0M$15.0M
Net earnings/(loss) attributable to BMS$7.1B-$8.9B$8.0B
Basic (in dollars per share)$3.47-$4.41$3.88
Diluted (in dollars per share)$3.46-$4.41$3.86

Compare Bristol-Myers Squibb with another company

Corporate structure

Bristol-Myers Squibb sits at the top of its group. 150 entities, 51 countries on record. Switch between the flow chart and the network, and select any entity to see its details.

Major holders of Bristol-Myers Squibb

  • State Street Corporation Filed SCHEDULE 13G on Bristol-Myers Squibb, latest Aug 7, 2026
  • VANGUARD CAPITAL MANAGEMENT LLC Filed SCHEDULE 13G on Bristol-Myers Squibb, latest Apr 29, 2026
  • VANGUARD GROUP INC Filed SCHEDULE 13G/A on Bristol-Myers Squibb, latest Mar 26, 2026 (4 filings since Feb 9, 2022)
  • JPMorgan Chase Filed SCHEDULE 13G/A on Bristol-Myers Squibb, latest Oct 31, 2025 (2 filings since Apr 25, 2025)
  • BlackRock Filed SCHEDULE 13G/A on Bristol-Myers Squibb, latest Apr 17, 2025 (4 filings since Feb 1, 2022)

Built from parent and subsidiary links from GLEIF, the Global Legal Entity Identifier Foundation (CC0); subsidiaries listed in Exhibit 21 of annual reports filed with the SEC; subsidiaries, stakes and holdings from Wikidata (CC0); major holders from Schedules 13D and 13G; stakes of 5% or more it reported on Schedules 13D and 13G (7 companies). Each entity in the chart links to its source.

What it owns

What Bristol-Myers Squibb reports owning in its annual reports to the SEC: buildings, land and equipment, real estate and locations, investments, intangible assets and inventory, at the end of its latest fiscal year and a year before.

Property and equipment

ItemLatestA year beforeChange
Land$157.0M14 Dec 31, 2025$161.0M14 Dec 31, 2024−2.5%
Buildings and improvements$7.3B14 Dec 31, 2025$6.6B14 Dec 31, 2024+10.5%
Machinery and equipment$3.8B14 Dec 31, 2025$3.8B14 Dec 31, 2024−0.7%
Construction in progress$1.6B14 Dec 31, 2025$1.5B14 Dec 31, 2024+6.2%
Property and equipment, before depreciation$12.8B14 Dec 31, 2025$12.1B14 Dec 31, 2024+6.2%
Accumulated depreciation$5.3B14 Dec 31, 2025$4.9B14 Dec 31, 2024+7.0%
Property and equipment, net$7.5B14 Dec 31, 2025$7.1B14 Dec 31, 2024+5.7%
Operating-lease assets (leased space)$1.6B14 Dec 31, 2025$1.2B14 Dec 31, 2024+29.2%

Investments

ItemLatestA year beforeChange
Cash and cash equivalents$10.2B14 Dec 31, 2025$10.3B14 Dec 31, 2024−1.3%
Marketable securities, current$464.0M14 Dec 31, 2025$513.0M14 Dec 31, 2024−9.6%
Marketable securities, non-current$396.0M14 Dec 31, 2025$320.0M14 Dec 31, 2024+23.8%
Equity securities at fair value$552.0M14 Dec 31, 2025$289.0M14 Dec 31, 2024+91.0%
Stakes in other companies (equity method)$738.0M14 Dec 31, 2025$598.0M14 Dec 31, 2024+23.4%

Intangibles and goodwill

ItemLatestA year beforeChange
Goodwill$21.8B14 Dec 31, 2025$21.7B14 Dec 31, 2024+0.2%
Intangible assets, net (excluding goodwill)$19.1B14 Dec 31, 2025$23.3B14 Dec 31, 2024−18.0%
Accumulated amortization$53.3B14 Dec 31, 2025$50.0B14 Dec 31, 2024+6.6%

Inventory

ItemLatestA year beforeChange
Inventory, total$2.7B14 Dec 31, 2025$2.6B14 Dec 31, 2024+5.2%
Work in process$3.2B14 Dec 31, 2025$2.5B14 Dec 31, 2024+23.9%
Finished goods$900.0M14 Dec 31, 2025$1.3B14 Dec 31, 2024−28.4%

Properties, in its own words

Our principal executive offices are located at Route 206 & Province Line Road, Princeton, NJ. We own or lease manufacturing, R&D, administration, storage and distribution facilities at approximately 130 sites worldwide. We believe our manufacturing properties, in combination with our third-party manufacturers, are in good operating condition and provide adequate production capacity for our current and projected operations. We also believe that none of our properties are subject to any material encumbrance, easement or other restriction that would detract materially from their value or impair their use in the operation of the business. For further information about our manufacturing properties, refer to “Item 1. Business—Manufacturing and Quality Assurance.”

Our significant manufacturing and R&D locations by geographic area were as follows at December 31, 2025:

The rest of Item 2

Manufacturing · R&D

United States · 4 · 7

International · 4 · 1

Total · 8 · 8

Item 2 of the 10-K filed Feb 11, 2026.22

The story

Squibb

The Squibb corporation was founded in 1858 by Edward Robinson Squibb in Brooklyn, New York after resigning from his assistant surgeon post from the U.S. Navy. The company started operating in a small brick laboratory in Brooklyn. It was reported that the nascent company almost closed upon its opening as the facility burned down on Christmas Eve of 1858. While the laboratory was destroyed, a group of doctors and surgeons helped Squibb reopen in 1859 by subscribing $2,100. The business survived and flourished.

Squibb was known as an advocate of quality control and high purity standards early within the pharmaceutical industry. He went on to self-publish an alternative to the U.S. Pharmacopeia titled Squibb's Ephemeris of Materia Medica, after failing to convince the American Medical Association to incorporate higher purity standards.

Materia Medica, Squibb products, and Edward Squibb's opinion on the fundamentals of pharmacy are found in many medical papers of the late 1800s. The American Journal of Pharmacy published more than one hundred papers of Squibb's research surrounding the industry. When Squibb's health deteriorated, management was passed down to his sons, Charles and Edward. By 1895, the company officially became E.R. Squibb & Sons.

The sons of Edward Squibb sold the company to Lowell M. Palmer and Theodore Weicker in 1905, who incorporated the company. Around this time, the Squibb logo was developed, which represented the company's products of "uniformity, purity, efficacy, and reliability based on research."

Squibb Corporation served as a major supplier of medical goods to the Union Army during the American Civil War, providing portable medical kits containing morphine, surgical anesthetics, and quinine for the treatment of malaria (which was endemic in most of the Eastern United States at that time).

In 1944, Squibb opened the world's largest penicillin plant in New Brunswick, New Jersey.

Bristol-Myers

In 1887, Hamilton College graduates William McLaren Bristol and John Ripley Myers purchased the Clinton Pharmaceutical company of Clinton, New York. In May 1898, they decided to rename it Bristol, Myers and Company. Following Myers' death in 1899, Bristol changed the name to the Bristol-Myers Corporation.

During the 1890s, the company introduced its first nationally recognized product Sal Hepatica, a laxative mineral salt, followed by Ipana toothpaste in 1901. Other divisions were Clairol (hair colors and haircare) and Drackett (household products such as Windex and Drano).

Read the full text

In 1943, Bristol-Myers acquired Cheplin Biological Laboratories, a producer of acidophilus milk in East Syracuse, New York, and converted the plant to produce penicillin for the World War II Allied forces. After the war, the company renamed the plant Bristol Laboratories in 1945 and entered the civilian antibiotics market, where it faced competition from Squibb.

Penicillin production at the East Syracuse plant ended in 2005, when it became less expensive to produce overseas. As of 2010, the facility was used for the manufacturing process development and production of other biologic medicines for clinical trials and commercial use.

Merger

In 1989, Bristol-Myers and Squibb merged and became Bristol-Myers Squibb.

In 1999, then-U.S. President Bill Clinton awarded Bristol-Myers Squibb the National Medal of Technology, the nation's highest recognition for technological achievement, "for extending, and enhancing human life through innovative pharmaceutical research and development and for redefining the science of clinical study through groundbreaking and hugely complex clinical trials that are recognized models in the industry."

2000 to 2010

In July 2006, the FBI raided the company's corporate offices on charges of collusion centered on the distribution of Plavix On 12 September 2006, the monitor, former Federal Judge Frederick B. Lacey, urged the company to remove then-CEO Peter Dolan over the Plavix dispute. Later that day, BMS announced that Dolan would indeed step down. The deferred prosecution agreement expired in June 2007 and the Department of Justice did not take any further legal action against the company for matters covered by the DPA. Under CEO Jim Cornelius, who was CEO following Dolan until May 2010, all executives involved in the "channel-stuffing" and generic competition scandals have since left the company.

In 2009, the company began a major restructuring focusing on the pharmaceutical business and biologic products, along with productivity initiatives and cost-cutting and streamlining business operations through a multiyear program of on-going layoffs. This was part of a business strategy launched in 2007 to transform the company from a large, diversified pharmaceutical company to a specialty biopharma company, which also included the closure of half of its manufacturing facilities. As another cost-cutting measure, Bristol-Myers Squibb also reduced health-care subsidies for retirees and planned to freeze their pension plan at the end of 2009.

Lamberto Andreotti was named CEO in 2010; he had previously served as president and COO

2010-present

In 2010, Lou Schmukler joined Bristol-Myers Squibb as the president of global product development and design. Schmukler led the team that completed the company's strategic transformation to a specialty biopharmaceutical company that had begun in 2007. As of 2011, the company had a dozen manufacturing facilities and six product development sites.

The company was ranked as the best drug company of 2013 by Forbes magazine.

In December 2014, the company received FDA approval for the use of the PD-1 inhibitor nivolumab (Opdivo) in treating patients whose skin cancer cannot be removed or have not responded to previous drug therapies. In February 2015, the company initiated a research partnership with Rigel Pharmaceuticals which could generate more than $339 million. In March, the company obtained an exclusive opportunity to both licence and commercialise PROSTVAC, Bavarian Nordic's phase III prostate-specific antigen targeting cancer immunotherapy. Bavarian Nordic would receive an upfront payment of $60 million and incremental payments up to $230 million, if the overall survival of test patients exceeds that seen in Phase II tests. Bavarian could also receive milestone payments of between $110 million and $495 million, dependent on regulatory authorization, and these payments have the potential to total up to $975 million.

In May 2015, Giovanni Caforio became CEO of the company; Caforio was formerly the company's COO and succeeded Lamberto Andreotti upon his retirement. Andreotti subsequently succeeded James Cornelius as Executive Chairman upon his retirement.

From Wikipedia’s article on Bristol Myers Squibb, shared under CC BY-SA 4.0.8

Leadership

Who has led Bristol-Myers Squibb, and when. Pick a name to see everywhere that person has worked.

Board members and other officers (104)

Products and brands

Out of production

Sal Hepatica

Ipana

Divested brands

(Former Bristol-Myers brands, now divested)

Bufferin

Read the full text

Excedrin

Ban Deodorant

Vitalis (hair tonic)

Ammens (medicated powder)

Final Net (hair spray)

Comtrex (cold relief capsules)

Keri (lotion)

Products under development

The following is a selective list of investigational products under development, as of 2023:

Luspatercept - phase III: On 28 August 2023, BMS' drug Reblozyl has received FDA label expansion, making it a first-line treatment option for anemia in adults with low- to intermediate-risk myelodysplastic syndromes (MDS) who may need regular blood transfusions. This decision, supported by data from the Phase III COMMANDS study, highlights Reblozyl's superiority over erythropoiesis-stimulating agents (ESAs) in treating MDS-related anemia, potentially driving the drug's sales towards its $4 billion sales goal by 2030. The drug's efficacy in patients both with and without specific symptoms further widens its scope of application.

Beclabuvir (BMS-791325) – phase III

BMS-906024 – phase I

BMS-955176 – phase II

Brivanib alaninate (BMS-582664) – development terminated

Elotuzumab (BMS-901608) – phase III

Fostemsavir (BMS-663068) – approved in the United States in July 2020

Lirilumab (BMS-986015)

Lulizumab pegol (BMS-931699) – phase II

From Wikipedia’s article on Bristol Myers Squibb, shared under CC BY-SA 4.0.8

Subsidiaries and ownership

Subsidiaries

Also consolidated

Subsidiaries (Exhibit 21)

  • 1096271 BC ULC Canada9
  • 9643435 Canada Inc. Canada9
  • Abraxis BioScience Australia Pty Ltd. Australia9
  • BMS Holdings Netherlands Beta B.V. Netherlands9
  • BMS Ireland Capital Funding Designated Activity Company Ireland9
  • BMS Netherlands Operations B.V. Netherlands9
  • BMS Pharmaceutical Korea Limited Korea, Republic of9
  • BMS Pharmaceuticals Germany Holdings B.V. Netherlands9
  • BMS Pharmaceuticals International Holdings Netherlands B.V. Netherlands9
  • BMS Pharmaceuticals Korea Holdings B.V. Netherlands9
  • BMS Pharmaceuticals Mexico Holdings B.V. Netherlands9
  • BMS Pharmaceuticals Netherlands Holdings B.V. Netherlands9
  • Bristol Myers Squibb Regional Headquarter Company Saudi Arabia9
  • Bristol-Myers (Private) Limited Zimbabwe9
  • Bristol-Myers Squibb (Beijing) Innovation Pharmaceutical Technology Co., Ltd. China9
  • Bristol-Myers Squibb (China) Investment Co., Ltd. China9
  • Bristol-Myers Squibb (China) Pharmaceuticals Co., Ltd. China9
  • Bristol-Myers Squibb (Israel) Ltd. Israel9
  • Bristol-Myers Squibb (NZ) Limited New Zealand9
  • Bristol-Myers Squibb (Proprietary) Limited South Africa9
  • Bristol-Myers Squibb (Shanghai) Trading Co. Ltd. China9
  • Bristol-Myers Squibb (Singapore) Pte. Limited Singapore9
  • Bristol-Myers Squibb A.E. Greece9
  • Bristol-Myers Squibb Aktiebolag Sweden9
All 132 listed subsidiaries
  • Bristol-Myers Squibb Argentina S. R. L. Argentina9
  • Bristol-Myers Squibb Australia Pty. Ltd. Australia9
  • Bristol-Myers Squibb B.V. Netherlands9
  • Bristol-Myers Squibb Belgium S.A. Belgium9
  • Bristol-Myers Squibb Business Services India Private Limited India9
  • Bristol-Myers Squibb Business Services Limited United Kingdom9
  • Bristol-Myers Squibb Canada International Limited Canada9
  • Bristol-Myers Squibb Delta Company Limited Ireland9
  • Bristol-Myers Squibb Denmark Filial of Bristol-Myers Squibb AB Denmark9
  • Bristol-Myers Squibb EMEA Sarl France9
  • Bristol-Myers Squibb Egypt, LLC Egypt9
  • Bristol-Myers Squibb Epsilon Holdings Unlimited Company Ireland9
  • Bristol-Myers Squibb Farmaceutica Ltda. Brazil9
  • Bristol-Myers Squibb Farmaceutica Portuguesa S.A. Portugal9
  • Bristol-Myers Squibb Ges mbH. Austria9
  • Bristol-Myers Squibb GmbH & Co. KGaA Germany9
  • Bristol-Myers Squibb Hanbai K.K Japan9
  • Bristol-Myers Squibb Holding Germany GmbH & Co. KG Germany9
  • Bristol-Myers Squibb Holdings 2002 Limited United Kingdom9
  • Bristol-Myers Squibb Holdings Germany Verwaltungs GmbH Germany9
  • Bristol-Myers Squibb Holdings Ireland Unlimited Company Ireland9
  • Bristol-Myers Squibb Holdings Limited United Kingdom9
  • Bristol-Myers Squibb Holdings Pharma Ltd. Liability Company Switzerland9
  • Bristol-Myers Squibb India Pvt. Limited India9
  • Bristol-Myers Squibb International Company Unlimited Company Ireland9
  • Bristol-Myers Squibb K.K. Japan9
  • Bristol-Myers Squibb Kft. Hungary9
  • Bristol-Myers Squibb Limited Liability Company Russian Federation9
  • Bristol-Myers Squibb MEA GmbH Switzerland9
  • Bristol-Myers Squibb Manufacturing Company Unlimited Company Ireland9
  • Bristol-Myers Squibb Marketing Services S.R.L. Romania9
  • Bristol-Myers Squibb Middle East & Africa FZ-LLC United Arab Emirates9
  • Bristol-Myers Squibb Norway AS Norway9
  • Bristol-Myers Squibb Peru S.A. Peru9
  • Bristol-Myers Squibb Pharma (HK) Ltd Hong Kong9
  • Bristol-Myers Squibb Pharma (Thailand) Limited Thailand9
  • Bristol-Myers Squibb Pharma EEIG Ireland9
  • Bristol-Myers Squibb Pharmaceuticals Limited United Kingdom9
  • Bristol-Myers Squibb Pharmaceuticals Unlimited Company Ireland9
  • Bristol-Myers Squibb Polska Sp. z o.o. Poland9
  • Bristol-Myers Squibb Products S.A. Switzerland9
  • Bristol-Myers Squibb Romania S.R.L. Romania9
  • Bristol-Myers Squibb S.r.l. Italy9
  • Bristol-Myers Squibb SA Switzerland9
  • Bristol-Myers Squibb SAS France9
  • Bristol-Myers Squibb Service Ltd. Bermuda9
  • Bristol-Myers Squibb Services Sp. z o.o. Poland9
  • Bristol-Myers Squibb Services Unlimited Company Ireland9
  • Bristol-Myers Squibb Spol. s r.o. Czech Republic9
  • Bristol-Myers Squibb TGF Beta Inc. Canada9
  • Bristol-Myers Squibb Trustees Ltd. United Kingdom9
  • Bristol-Myers Squibb Verwaltungs GmbH Germany9
  • Bristol-Myers Squibb de Colombia S.A. Colombia9
  • Bristol-Myers Squibb de Mexico, S. de R.L. de C.V. Mexico9
  • Bristol-Myers Squibb, S.A.U. Spain9
  • Bristol-Myers Squibb/Astrazeneca EEIG United Kingdom9
  • Bristol-Myers Squibb/Pfizer EEIG Ireland9
  • Celgene Chemicals Sarl Switzerland9
  • Celgene Distribution B.V. Netherlands9
  • Celgene Europe B.V. Netherlands9
  • Celgene Europe Limited United Kingdom9
  • Celgene Global Holdings Sarl Switzerland9
  • Celgene International Holdings Corporation, Prodruznica v Sloveniji Slovenia9
  • Celgene International II Sàrl Switzerland9
  • Celgene International Sàrl Switzerland9
  • Celgene Limited Hong Kong9
  • Celgene Logistics Sarl Switzerland9
  • Celgene Logistics Sarl (Sucursale Mexico) Mexico9
  • Celgene Netherlands BV Netherlands9
  • Celgene Netherlands Investment BV Netherlands9
  • Celgene Pharmaceutical (Shanghai) Company Limited China9
  • Celgene Pty Limited Australia9
  • Celgene Puerto Rico Distribution LLC Puerto Rico9
  • Celgene R&D Sarl Switzerland9
  • Celgene RIVOT SRL Barbados9
  • Celgene Receptos Limited United Kingdom9
  • Celgene Receptos Sàrl Switzerland9
  • Celgene Research SL Spain9
  • Celgene Research and Development I ULC Canada9
  • Celgene Sdn Bhd Malaysia9
  • Celgene Switzerland Holdings Sarl Switzerland9
  • Celgene Sàrl AU Morocco9
  • Celgene UK Distribution Limited United Kingdom9
  • Celgene UK Holdings Limited United Kingdom9
  • Celgene UK Manufacturing (II) Limited United Kingdom9
  • Celgene UK Manufacturing (III) Limited United Kingdom9
  • Celgene UK Manufacturing Limited United Kingdom9
  • Celgene d.o.o. Croatia9
  • Celgene s.r.o. Slovakia9
  • Celgene, S. de R.L. de C.V. Mexico9
  • Celmed Ltd. Bermuda9
  • Cormorant Pharmaceuticals AB Sweden9
  • E. R. Squibb & Sons Limited United Kingdom9
  • Forbius PTY Limited Australia9
  • Foxtrot Acquisition Sub ULC Canada9
  • Grove Insurance Company Ltd. Bermuda9
  • Linson Investments Limited Cayman Islands9
  • Mirati Therapeutics (Suisse) GmbH Switzerland9
  • Mirati Therapeutics B.V. Netherlands9
  • MyoKardia Australia Pty Ltd Australia9
  • Oy Bristol-Myers Squibb (Finland) AB Finland9
  • RayzeBio Pharmaceuticals (Chengdu) Co., Ltd. China9
  • SPV A Holdings ULC Canada9
  • Sino-American Shanghai Squibb Pharmaceuticals Limited China9
  • Squibb Middle East S.A. Panama9
  • Swords Laboratories Unlimited Company Ireland9
  • The Representative Office of Celgene International Holdings Corporation in Moscow Russian Federation9
  • Westwood-Intrafin SA Switzerland9

From Wikidata.1 Ownership links from GLEIF, the Global Legal Entity Identifier Foundation (CC0); each one cites its LEI record. The subsidiaries the company lists in Exhibit 21 of its annual report, as filed.

Acquisitions

In August 2009, during a major restructuring activity, BMS acquired the biotechnology firm Medarex as part of the company's "String of Pearls" strategy of alliances, partnerships, and acquisitions. In November 2009, Bristol Myers Squibb announced that it was "splitting off" Mead Johnson Nutrition by offering BMY shareholders the opportunity to exchange their stock for shares in Mead Johnson. According to Bristol Myers Squibb, this move was expected to further sharpen the company's focus on biopharmaceuticals.

In October 2010, the company acquired ZymoGenetics, securing an existing product, as well as pipeline assets in hepatitis C, cancer, and other therapeutic areas.

Bristol Myers Squibb agreed to pay around $2.5 billion in cash to buy Inhibitex Inc. in attempt to compete with Gilead/Pharmasset to produce hepatitis C drugs. The settlement will be finished in 2 months for its Inhibitex's shareholders acceptance of 126% premium price of its price over the previous 20 trading days ended on 6 January. On 29 June, BMS extended its portfolio of diabetes treatments when it agreed to buy Amylin Pharmaceuticals for around US$5.3 billion in cash and pay US$1.7 billion to Eli Lilly to cover Amylin's debt and its outstanding collaboration-related obligations. AstraZeneca, which already collaborated on several diabetes treatments with BMS, agreed to pay US$3.4 billion in cash for the right to continue development of Amylin's products. Two years later, the company divested Amylin to AstraZeneca.

In April 2014, BMS announced its acquisition of iPierian for up to $725 million.

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In February 2015, the company acquired Flexus Biosciences for $1.25 billion. As part of this deal, BMS will gain full rights to Flexus' lead small molecule IDO1-inhibitor, F001287. In November, the company acquired the cardiovascular disease drug developer Cardioxyl for up to $2.075 billion. The deal strengthens the BMS' critical pipelines with the phase II candidate for acute decompensated heart failure, CXL-1427.

In March 2016, the company announced it would acquire Padlock Therapeutics for up to $600 million. In early July, the company announced it would acquire Cormorant Pharmaceuticals for $520 million, boosting BMS' oncology offering through Cormorants monoclonal antibody targeted against interleukin-8.

In August 2017, the company acquired IFM Therapeutics for $300 million upfront, with contingency payments of $1.01 billion due on certain milestones – allowing BMS to better compete against Merck & Co's cancer rival treatment, Keytruda.

In November 2019, the company acquired Celgene for $74 billion or $95 billion including debt. To gain regulatory approval, Amgen acquired Otezla from Celgene for $13.4 billion. The Celgene acquisition aimed to be a refresher to the company's pipeline, helping to overcome from declining sales of Opdivo relative to competitor Keytruda. BMS investors Wellington Management Company and Starboard Value opposed the merger; however, 75% of its shareholders voted to approve.

In July 2019, the company sold its consumer health business, UPSA, to Taisho Pharmaceutical. UPSA focused product delivery on France and the rest of Europe. As early as 2005, the company had divested individual consumer products, and its US- and Canada-focused consumer products business.

In February 2020, BMS and partner Biomotiv launched a new company called Anteros Pharmaceuticals, which focuses on creating inflammation and fibrosis medicines. In August, the business announced it would acquire Forbius and its TGF-beta 1 & TGF-beta 3 inhibitors. In October, BMS announced it would acquire cardiology company MyoKardia for $13.1 billion ($225 per share) gaining control of mavacamten, a cardiovascular drug for obstructive hypertrophic cardiomyopathy (HCM), and the development of two key treatments: danicamtiv (MYK-491) and MYK-224.

In August 2022, BMS acquired Turning Point Therapeutics for $4.1 billion in cash, helping to boost its complement of cancer drugs, specifically repotrectinib. That same month, the company announced it would be investing $180m in French AI company Owkin, to design potentially more precise and efficient clinical trials. The collaboration will initially focus on cardiovascular diseases, and has the potential to extend into projects in other therapeutic areas.

In August 2023, Bristol Myers Squibb partnered with Cellares for the robotic production of CAR-T treatments of which it has two approved. In September 2023, BMS announced it would pay Zenas BioPharma $50m upfront for a strategic license and collaboration to develop and commercialise obexelimab, a novel, bi-functional antibody for autoimmune diseases.

In January 2024, BMS acquired Mirati Therapeutics, an American biotechnology company that develops targeted therapies for the treatment of cancer, for $4.8 billion, and an additional $1 billion in milestone payment.

In March 2024, BMS acquired Karuna Therapeutics for $14 billion. The acquisition included Karuna's lead asset, KarXT, an investigational muscarinic antipsychotic combination of Xanomeline and Trospium for the treatment of schizophrenia in adults.

In February 2024, the company acquired RayzeBio for approximately $4.1 billion.

In September 2024, the Food and Drug Administration approved Cobenfy, the first novel type of treatment for schizophrenia in 70 years.

List of mergers and acquisitions

The following is an illustration of the company's major mergers and acquisitions and historical predecessors:

From Wikipedia’s article on Bristol Myers Squibb, shared under CC BY-SA 4.0.8

Employees over time

  • 201930,0001

Timeline

  1. Jul 30, 20268-K Results of operations; Regulation FD disclosure139
  2. May 8, 20268-K Shareholder vote140
  3. Apr 30, 20268-K Results of operations; Regulation FD disclosure141
  4. Feb 5, 20268-K Results of operations; Regulation FD disclosure142
  5. Jan 12, 20268-K Regulation FD disclosure143
  6. Nov 18, 20258-K Other events144
  7. Nov 10, 20258-K Other events145
  8. Nov 3, 20258-K Other events146
  9. Oct 30, 20258-K Results of operations; Regulation FD disclosure147
  10. Jul 31, 20258-K Results of operations; Regulation FD disclosure148
  11. Jul 25, 20258-K Executive or director change149
  12. May 7, 20258-K Shareholder vote150
  13. Nov 3, 2023New chief executive Christopher S. Boerner becomes CEO23
  14. May 2015New chief executive Giovanni Caforio becomes CEO1
  15. May 2010New chief executive Lamberto Andreotti becomes CEO1
  16. Nov 3, 2006New chief executive James M. Cornelius becomes CEO26
  17. Sep 12, 2003New chief executive Peter R. Dolan becomes CEO27
  18. 1989Founded Founded in Clinton1

Calendar

Coming up

  1. Oct 29, 2026 · Before the openReports results for the quarter ending Sep/2026 A year earlier it reported $1.63 a share, on Oct 30, 2025.151

When it reported results

  1. Jul 30, 2026Reported quarterly or annual results139
  2. Apr 30, 2026Reported quarterly or annual results141
  3. Feb 5, 2026Reported quarterly or annual results142
  4. Oct 30, 2025Reported quarterly or annual results147
  5. Jul 31, 2025Reported quarterly or annual results148
  6. Apr 24, 2025Reported quarterly or annual results152
  7. Feb 6, 2025Reported quarterly or annual results153
  8. Oct 31, 2024Reported quarterly or annual results154

Upcoming dates from Nasdaq's calendar; past results from the company's 8-K filings (Item 2.02). The full markets calendar

Filings

552 filings to the SEC since October 2021: 5 annual reports, 15 quarterly reports, 58 major events, 371 insider forms, 12 large holders, 91 other. The latest 20:

  1. Oct 5, 20264 EDGAR
  2. Oct 2, 20264 EDGAR
  3. Oct 2, 20264 EDGAR
  4. Oct 2, 20264 EDGAR
  5. Oct 2, 20264 EDGAR
  6. Oct 2, 20264 EDGAR
  7. Sep 10, 20264 EDGAR
  8. Sep 9, 2026144 EDGAR
  9. Sep 3, 20264 EDGAR
  10. Aug 26, 20264 EDGAR
  11. Aug 25, 2026144 EDGAR
  12. Aug 7, 2026SCHEDULE 13G EDGAR
  13. Aug 4, 20264 EDGAR
  14. Aug 4, 20264 EDGAR
  15. Jul 30, 202610-Q EDGAR
  16. Jul 30, 20268-K EDGAR
  17. Jul 2, 20264 EDGAR
  18. Jul 2, 20264 EDGAR
  19. Jul 2, 20264 EDGAR
  20. Jul 2, 20264 EDGAR

The 552 filings since October 2021 can be filtered by form type and year here when JavaScript is on.

Every filing from the last five years, summarized. The full record is on SEC EDGAR.

Insider trades

36 open-market trades by officers, directors and large owners since October 2021: 7 buys and 29 sales. Grants, option exercises and gifts are left out.

DateWhoTradeSharesPriceValueFiling
Sep 9, 2026Massacesi CristianEVP,Chief Med Offr,Head of DevSale6,249$64.57$403.5KForm 4
Aug 25, 2026Holzer Phil MSVP and ControllerSale500$67.50$33.8KForm 4
Apr 1, 2026Elkins David VEVP, Chief Financial OfficerSale30,000$61.67$1.9MForm 4
Sep 2, 2025Elkins David VEVP, Chief Financial OfficerSale56,000$47.33$2.7MForm 4
Aug 2, 2025Short Bartie WendyEVP, Corporate AffairsSale378$44.23$16.7KForm 4
May 9, 2025Hickey BenjaminPresident, RayzeBio Org.Sale97$38.01$3.7KForm 4
Apr 25, 2025Hirawat SamitEVP,Chief Med.Offr.,Drug Dev.Buy4,250$47.58$202.2KForm 4
Feb 20, 2025BOERNER CHRISTOPHER S.Chief Executive OfficerBuy2,000$55.05$110.1KForm 4
Feb 14, 2025Hirawat SamitEVP,Chief Med.Offr.,Drug Dev.Buy1,823$54.84$100.0KForm 4
Nov 4, 2024Holzer Phil MSVP and ControllerSale700$55.62$38.9KForm 4
Nov 1, 2024Hirawat SamitEVP,Chief Med.Offr.,Drug Dev.Buy1,830$54.67$100.1KForm 4
Dec 5, 2023BOERNER CHRISTOPHER S.Chief Executive OfficerBuy2,000$49.78$99.6KForm 4
Nov 28, 2023BOERNER CHRISTOPHER S.Chief Executive OfficerBuy3,071$48.86$150.0KForm 4
Nov 20, 2023Samuels Theodore R. IIDirectorBuy8,500$49.81$423.4KForm 4
Aug 24, 2023Powell AnnEVP, Chief Human ResourcesSale17,986$61.25$1.1MForm 4
Aug 3, 2023Plenge Robert MEVP, Chief Research OfficerSale732$61.14$44.8KForm 4
May 3, 2023VESSEY RUPERTEVP & President, ResearchSale50,385$67.06$3.4MForm 4
Feb 6, 2023Caforio GiovanniExecutive Chair of the BoardSale240,000$74.65$17.9MForm 4
Feb 6, 2023Powell AnnEVP, Chief Human ResourcesSale11,183$74.69$835.3KForm 4
Nov 9, 2022Powell AnnEVP, Chief Human ResourcesSale16,250$80.45$1.3MForm 4

All 36 trades can be filtered by person here when JavaScript is on.

From Forms 4 filed with the SEC.

Major holders

Investors who own more than 5% of the shares must tell the SEC: a 13D if they may seek to influence the company, a 13G if they hold passively.

Stakes it holds

Bristol-Myers Squibb has told the SEC it owns more than 5% of 7 companies, latest first (Schedules 13D and 13G).

Executive pay

What the company paid its top executives, from the summary compensation table in its proxy statement. Total pay includes salary, bonus, stock and option awards and other pay, as the company valued them.

YearExecutiveAgeSalaryTotal pay
2025Christopher S. Boerner, Ph.D.Board Chair and Chief Executive Officer$1.6M$21.9M167
2025Samit HirawatM.D. Former EVP, Chief Medical Officer, Head of Development$964.9K$10.3M167
2025Cristian MassacesiM.D. EVP, Chief Medical Officer, Head of Development$388.5K$10.1M167
2025Adam LenkowskyEVP, Chief Commercialization Officer$1.1M$9.3M167
2025David V. ElkinsEVP and Chief Financial Officer$1.1M$9.2M167
2025Greg MeyersEVP, Chief Digital and Technology Officer$1.1M$7.2M167
2024Christopher S. Boerner, Ph.D.Board Chair and Chief Executive Officer$1.5M$18.8M167
2024David V. ElkinsEVP and Chief Financial Officer$1.1M$8.7M167
2024Samit HirawatM.D. Former EVP, Chief Medical Officer, Head of Development$1.1M$8.6M167
2023Christopher S. Boerner, Ph.D.Board Chair and Chief Executive Officer$1.3M$8.5M167
2023David V. ElkinsEVP and Chief Financial Officer$1.1M$7.2M167
2023Samit HirawatM.D. Former EVP, Chief Medical Officer, Head of Development$1.1M$6.2M167

Held by these funds

The largest holders among investment managers' 13F reports for the quarter ending Jun 30, 2026, the top 25 of 100. Change is in shares since the quarter before.

FundSharesValueShare of the fundChange
BlackRock, Inc.180,384,994$10.4B0.2%+8,702,106
Vanguard Capital Management LLC133,337,856$7.7B0.2%+1,017,616
State Street Corp102,408,940$5.9B0.2%+3,844,026
Jpmorgan Chase & Co71,713,442$4.2B0.2%−20,761,752
Charles Schwab Investment Management Inc67,595,177$3.9B0.5%+6,479,804
Geode Capital Management, LLC56,443,077$3.2B0.2%+1,156,903
Vanguard Portfolio Management LLC46,873,015$2.7B0.1%+642,860
Norges Bank36,866,658$2.1B0.2%New
Bank Of America Corp /de/34,045,352$2.0B0.1%+1,458,371
Morgan Stanley29,009,025$1.7B0.1%−189,529
Aqr Capital Management LLC27,357,486$1.6B0.5%−2,273,619
Ameriprise Financial Inc26,670,064$1.5B0.3%+199,346
Primecap Management Co/ca/24,923,900$1.4B0.8%−61,249
Northern Trust Corp24,918,384$1.4B0.2%+159,613
UBS AM, a distinct business unit of UBS ASSET MANAGEMENT AMERICAS LLC22,839,010$1.3B0.2%+119,690
Bank of New York Mellon Corp21,821,384$1.3B0.2%−1,479,953
Independent Franchise Partners LLP21,792,841$1.3B8.2%+517,367
Dimensional Fund Advisors LP19,691,951$1.1B0.2%+929,362
Legal & General Group Plc17,022,940$980.9M0.2%+145,314
Goldman Sachs Group Inc17,016,799$980.5M0.1%+2,962,281
Pzena Investment Management LLC17,007,044$979.9M2.9%−88,687
Fmr LLC16,293,303$938.8M0.0%+5,622,200
Invesco Ltd.16,033,480$923.8M0.1%+523,481
Schroder Investment Management Group12,226,954$716.0M0.5%−8,540
Royal Bank Of Canada12,094,886$696.9M0.1%+1,136,184

13F reports cover disclosed long positions in U.S. stocks only.

Members of Congress who traded it

63 trades disclosed by members of Congress, the latest 25. “Vs S&P since” is the stock’s change since the trade minus the S&P 500’s.

DateMemberTradeAmountVs S&P sinceFiling
May 7, 2026Mike KellyRepublican, HouseSale$15,001 - $50,000−0.7%Report
Mar 27, 2026Alan ArmstrongRepublican, SenateBuy$1,001 - $15,000−19.6%Report
Dec 19, 2025Gilbert Ray Cisneros, Jr.Democratic, HouseBuy$1,001 - $15,000−3.1%Report
Dec 18, 2025Julie JohnsonDemocratic, HouseSale$1,001 - $15,000+2.1%Report
Nov 13, 2025Julie JohnsonDemocratic, HousePartial sale$1,001 - $15,000−8.0%Report
Nov 12, 2025Gilbert Ray Cisneros, Jr.Democratic, HouseBuy$1,001 - $15,000+8.8%Report
Oct 9, 2025Gilbert Ray Cisneros, Jr.Democratic, HousePartial sale$1,001 - $15,000−18.7%Report
Aug 14, 2025Julie JohnsonDemocratic, HousePartial sale$1,001 - $15,000−5.3%Report
Jun 24, 2025Virginia FoxxRepublican, HouseSale$1,001 - $15,000+0.1%Report
May 12, 2025Jefferson ShreveRepublican, HouseSale$15,001 - $50,000+8.4%Report
Apr 28, 2025Julia LetlowRepublican, HouseSale$1,001 - $15,000+16.8%Report
Apr 15, 2025Tommy TubervilleRepublican, SenateSale$1,001 - $15,000+24.1%Report
Apr 1, 2025Julie JohnsonDemocratic, HouseSale$1,001 - $15,000+37.2%Report
Mar 27, 2025Greg LandsmanDemocratic, HouseSale$1,001 - $15,000+34.7%Report
Jan 15, 2025Julie JohnsonDemocratic, HouseBuy$1,001 - $15,000−23.3%Report
Dec 6, 2024Virginia FoxxRepublican, HouseBuy$1,001 - $15,000−26.4%Report
Oct 29, 2024Val T. HoyleDemocratic, HouseBuy$1,001 - $15,000−18.9%Report
Oct 23, 2024Julia LetlowRepublican, HouseBuy$1,001 - $15,000−20.9%Report
Apr 3, 2024Tommy TubervilleRepublican, SenateBuy$1,001 - $15,000+34.1%Report
Apr 3, 2024Tommy TubervilleRepublican, SenateSale$1,001 - $15,000+34.1%Report
Jan 18, 2024John JamesRepublican, HouseSale$1,001 - $15,000+42.7%Report
Jan 9, 2024Rick LarsenDemocratic, HouseSale$1,001 - $15,000+46.3%Report
Jan 3, 2024Tommy TubervilleRepublican, SenatePartial sale$1,001 - $15,000+50.4%Report
Nov 16, 2023Tommy TubervilleRepublican, SenateSale$1,001 - $15,000−53.9%Report
Nov 10, 2023John JamesRepublican, HouseBuy$1,001 - $15,000−57.1%Report

Members report amounts as ranges, not exact figures. Returns are price-only (no dividends).

SEC filer profile

How Bristol-Myers Squibb is registered with the Securities and Exchange Commission, from its EDGAR record and the cover page of its latest annual report.

  • Name on EDGARBRISTOL MYERS SQUIBB CO2
  • CIK0000014272
  • Employer ID (EIN)22-079035022
  • Filer statusLarge accelerated filer not an emerging growth company; not a smaller reporting company; not a shell company22
  • Incorporated inDelaware22
  • Fiscal year endsDecember 312
  • Industry code (SIC)2834 Pharmaceutical Preparations2
  • SEC reviewing officeOffice of Life Sciences, Division of Corporation Finance2
  • Business addressRoute 206 And Province Line Road, Princeton, NJ 085432
  • Phone60925246212
  • Shares outstanding2,042,714,656 as of Jul 22, 202621
  • Public float$94.2B as of Jun 30, 202522
  • AuditorDELOITTE & TOUCHE LLP, Morristown, New Jersey PCAOB ID 34; it also attests to the company’s internal control over financial reporting22
  • On EDGAR sinceMar 15, 19942
  • Filings3,535 in all: 4 (2,061), 8-K (366), 4/A (101), 10-Q (98), 3 (85), 11-K (79), 425 (65), SC 13G/A (59)2
    All 61 form types

    NO ACT (54), CORRESP (51), SC TO-T/A (44), UPLOAD (38), DEFA14A (36), DEF 14A (33), 10-K (32), 8-K/A (26), SC 13G (26), 424B3 (25), SC 13D/A (22), SC TO-C (19), ARS (16), 424B5 (14), DFAN14A (13), S-8 (12), 3/A (11), FWP (11), SC 13D (10), SC TO-T (10), 5 (9), PRE 14A (9), 144 (8), S-3ASR (7), 10-Q/A (6), CT ORDER (6), PX14A6G (6), SC TO-I/A (6), SCHEDULE 13G/A (6), S-3 (5), S-4/A (5), S-8 POS (5), 8-A12B (4), S-3/A (4), S-4 (4), 10-K/A (3), CERT (3), SCHEDULE 13G (3), 25 (2), 25-NSE (2), 424B2 (2), EFFECT (2), 10-K405 (1), 15-12G (1), 25-NSE/A (1), 8-A12G (1), CERTNYS (1), DEFC14A (1), NT 10-Q (1), POSASR (1), PREC14A (1), PRRN14A (1), SC TO-I (1)

  • Latest filingsAnnual report (10-K) Feb 11, 2026
    Quarterly report (10-Q) Jul 30, 2026
    Proxy statement (DEF 14A) Mar 25, 2026
    Latest 8-K (8-K) Jul 30, 2026

Securities registered for trading

ClassSymbolExchange
Common Stock, $0.10 Par ValueBMYNew York Stock Exchange
Celgene Contingent Value RightsCELG RTNew York Stock Exchange
2.973% Notes due 2030BMY/30New York Stock Exchange
3.363% Notes due 2033BMY/33New York Stock Exchange
1.750% Notes due 2035BMY35New York Stock Exchange
3.857% Notes due 2038BMY/38New York Stock Exchange
4.289% Notes due 2045BMY/45New York Stock Exchange
4.581% Notes due 2055BMY/55New York Stock Exchange

From the cover page of the 10-K filed Feb 11, 2026 (Section 12(b) of the Exchange Act).22

Risk factors and legal proceedings

The risks Bristol-Myers Squibb names in Item 1A of its 10-K filed Feb 11, 2026: 47 risks under these headings, as written.22

  • Product, Industry and Operational Risks
  • Increased pricing pressure and other restrictions in the U.S. and abroad continue to negatively affect our revenues and profit margins.
  • unforeseen disruptions. Manufacturers that fail to comply with the IRA may be subject to various penalties, including civil monetary penalties, which could be significant. The IRA has and will continue to meaningfully impact our business strategies and those of others in the pharmaceutical industry. We continue to evaluate the impact of the IRA on our results of operations, and it is possible that these changes may result in a material impact on our business and results of operations.
  • In July 2025, the OBBBA was enacted which, among other things, aims to achieve efficiencies in U.S. federal government healthcare spending over the next decade, primarily within Medicaid. We are continuing to assess the full scope of this legislation and its potential commercial implications, and it is possible that these changes may impact our cash flows and results of operations.
  • We may experience difficulties or delays in the development and commercialization of new products. Our ability to replace revenue from products that lose patent protection is directly dependent on our ability to successfully develop and commercialize new products in a timely manner.
  • In addition, product extensions or additional indications may not be approved. Furthermore, products or indications approved under the U.S. FDA’s Accelerated Approval Program may be contingent upon verification and description of clinical benefit in confirmatory studies and such studies may not be successful. For additional information, refer to "Item 1. Business—Products, Intellectual Property and Product Exclusivity".
  • We are also unable to predict if and when any changes to laws or regulatory policies will occur and how they will affect our business and particularly our pipeline of new products.
  • We could lose market exclusivity of a product earlier than expected.
  • In the pharmaceutical and biotechnology industries, the majority of an innovative product’s commercial value is realized during its market exclusivity period. In the U.S. and in some other countries, when market exclusivity expires and generic versions are approved and marketed or when biosimilars are introduced (even if only for a competing product), there are usually very substantial and rapid declines in a product’s revenues.
  • In some cases, manufacturers may seek regulatory approval by submitting their own clinical study data to obtain marketing approval or choose to launch a generic product “at risk” before the expiration of the applicable patent(s) and/or before the final resolution of related patent litigation. In addition, some countries are allowing manufacturers to manufacture and sell generic products, which negatively impacts the protections afforded the Company. Lower-priced generics or biosimilars for BMS biologics or competing biologics could negatively impact our volumes and prices.
  • There is no assurance that a particular product will enjoy market exclusivity for the full time period that appears in the estimates disclosed in this 2025 Form 10-K or that we assume when we provide our financial guidance.
  • We face intense competition from other biopharmaceutical companies and manufacturers and expect to see increasing market penetration of lower-priced generic products.
The other 36 risks
  • In addition, we face competition from new products entering the market. New products may have (i) lower prices, (ii) superior efficacy (benefit) or safety (risk) profiles (whether actual or perceived), (iii) technological advantages that may make such products more convenient to use, (iv) better insurance coverage or reimbursement levels, (v) more effective marketing programs and/or other differentiating factors that make it harder for our products to compete. We cannot predict with accuracy the timing or impact of the
  • introduction of competitive products that treat diseases and conditions like those treated by our products and product candidates. Business combinations among our competitors and major third-party payers may also increase competition for our products. If we are unable to compete successfully against our competitors’ products in the marketplace, this could have a material negative impact on our revenues and earnings.
  • We could experience difficulties, delays and disruptions in our supply chain as well as in the manufacturing, distribution and sale of our products.
  • The U.S. and other countries have recently imposed, and may continue to impose, new tariffs. While pharmaceuticals are largely exempt from the tariffs imposed in 2025, such exemptions may be terminated or may not apply to any future tariffs. In accordance with the U.S. Government Agreement, BMS will receive certain U.S. tariff relief until January 2029. We continue to evaluate the impacts of tariffs on our business and results of operations, and it is possible that such tariffs, or future tariffs, may result in a material impact on our business and results of operations.
  • Regulatory, Intellectual Property, Litigation, Tax and Legal Compliance Risks
  • Litigation claiming infringement of intellectual property may adversely affect our future revenues and operating earnings.
  • Legal matters could negatively affect our business.
  • We are subject to a variety of U.S. and international laws and regulations.
  • Expectations relating to environmental, social and governance considerations and related reporting obligations expose the Company to potential liabilities, increased costs, reputational harm, and other adverse effects on the Company’s business.
  • brand and reputation, reduced demand for our products, inability to attract and retain employee talent or other negative impacts on our business and operations.
  • Changes to tax regulations could negatively impact our earnings.
  • The failure of third parties to meet their contractual, regulatory and other obligations could adversely affect our business.
  • Product labeling changes for our marketed products could result in a negative impact on revenues and profit margins.
  • In addition, if safety or efficacy concerns are raised about a third party's product in the same class as one of our products, those concerns could implicate the entire class and this, in turn, could have an adverse impact on the availability or commercial viability of our product(s) as well as other products in the class.
  • The illegal distribution and sale by third parties of counterfeit or unregistered versions of our products or stolen products could have a negative impact on our revenues, earnings, reputation and business.
  • Thefts of inventory at warehouses, plants or while in-transit, which are then not properly stored and are later sold through unauthorized channels that do not adhere to customary supply chain standards, could adversely impact patient safety, our reputation and our business. In addition, diversion of products from their authorized market into other channels may result in reduced revenues and negatively affect our profitability.
  • Use of social media platforms can present risks and challenges.
  • Information Technology and Cybersecurity Risks
  • We are dependent on information technology systems, including artificial intelligence programs, and face risk of cybersecurity incidents that could disrupt our business and result in theft of proprietary, confidential and personal information.
  • Strategic, Business Development and Employee Attraction and Retention Risks
  • We depend on several key products for most of our revenues, cash flows and earnings.
  • We derive a majority of our revenue and earnings from several key products. We expect that Eliquis, Opdivo, Opdivo Qvantig, Orencia, Reblozyl and Yervoy will represent a significant percentage of our revenue, earnings and cash flows during the next few years. A reduction in revenue from any of these products due to loss of market exclusivity or other factors could adversely impact our earnings and cash flows. For additional information, see “—We could lose market exclusivity of a product earlier than expected.”
  • Also, if one of our major products were to become subject to issues, such as loss of patent protection, significant changes in demand, formulary access changes, material product liability, unexpected side effects, regulatory proceedings, negative publicity, supply disruption from our manufacturing operations or third-party supplier or a significant advancement of competing products, we may incur an adverse impact on our business, financial condition, results of operations or the trading price of our stock.
  • In addition, in the U.S., most of our products are distributed through wholesalers, and if one of these wholesalers should encounter financial or other difficulties, we might be unable to timely collect the amounts that the wholesaler owes us, which could negatively impact our results of operations. We expect that consolidation and integration of pharmacy chains, wholesalers and pharmacy benefit managers will increase competitive and pricing pressures on pharmaceutical manufacturers, including us.
  • Third-party royalties represent a significant percentage of our pretax income and operating cash flow.
  • Failure to execute our business strategy or to identify and effectively manage acquisitions, divestitures, alliances, joint ventures and other portfolio actions could adversely impact our growth and profitability and our future results. In addition, any businesses or assets that we acquire in the future may underperform, we may not be able to successfully integrate them into our existing business and the occurrence of a number of unexpected factors could prevent or substantially delay the consummation of an anticipated acquisition, divestiture or merger.
  • Where we acquire debt or equity securities as all or part of the consideration for business development activities, such as in connection with a joint venture or acquisition, the value of those securities will fluctuate and may depreciate in value. We may not control the company in which we acquire securities, such as in connection with a collaborative arrangement, and as a result, we will have limited ability to determine its management, operational decisions, internal controls and compliance and other policies, which can result in additional financial and reputational risks.
  • We may not be successful in separating underperforming or non-strategic assets, and gains or losses on the divestiture of, or lost operating income from, such assets may affect our earnings. Our divestitures also may result in continued financial exposure to the divested businesses, such as through guarantees or other financial arrangements, continued supply and services arrangements, or potential litigation, following the transaction. Under these arrangements, nonperformance by us could result in obligations being
  • imposed on us that could have a material adverse effect on our competitive position, cash flows, results of operations, financial condition or reputation.
  • We might also incur asset impairment charges related to acquisitions or divestitures that reduce our earnings. The value allocated to certain of our assets could be substantially impaired due to a number of factors beyond our control. New or revised accounting standards, rules and interpretations could result in changes to the recognition of income and expense that may materially and adversely affect our financial results.
  • Failure to attract and retain a highly qualified workforce or to maintain our workplace culture could affect our ability to successfully develop and commercialize products.
  • Market, Liquidity and Credit Risks
  • We have significant indebtedness that could have negative consequences.
  • Adverse changes in U.S. and global economic and political conditions could adversely affect our operations and profitability.
  • competitive products enter the market or clinical trial results for our competitors’ products affect the value proposition for our product. Any such delays or difficulties in clinical development could also potentially lead to a material impairment of our intangible assets, including the $19.1 billion of other intangible assets as of December 31, 2025.
  • We cannot predict or reasonably estimate the impact of any potential long-term changes to the healthcare industry from global economic and political events, including any future pandemics. It is possible that changes in the healthcare system could impose additional burdens on clinical trials, which could increase the costs of sponsoring clinical trials or lead to additional delays or difficulties with completing clinical trials. We may also experience additional pricing pressures, shifts in the U.S. payer channel mix and/or increased governmental regulation.
  • There can be no guarantee that we will pay dividends or repurchase stock.
  • Our amended bylaws designate the Court of Chancery of the State of Delaware as the sole and exclusive forum for certain lawsuits between us and our stockholders, which could limit our stockholders’ ability to obtain a judicial forum that it finds favorable for such lawsuits and make it more costly for our stockholders to bring such lawsuits, which may have the effect of discouraging such lawsuits.
  • Nevertheless, this forum selection provision in our bylaws may limit a stockholder’s ability to bring a claim in a judicial forum that it finds favorable for disputes with us or any of our directors, officers and other employees, which may discourage lawsuits with respect to such claims, although our stockholders will not be deemed to have waived our compliance with federal securities laws and the rules and regulations thereunder. In addition, stockholders who do bring a claim in the Court of Chancery in the State of Delaware could
  • face additional litigation costs in pursuing any such claim, particularly if they do not reside in or near Delaware. While we believe the risk of a court declining to enforce the forum selection provision contained in our amended bylaws is low, if a court were to find the provision inapplicable to, or unenforceable in respect of, one or more of the specified types of actions or proceedings, we may incur additional costs associated with resolving such action in other jurisdictions, which could harm our business, operating results and financial condition.

Legal proceedings

Information pertaining to legal proceedings can be found in “Item 8. Financial Statements and Supplementary Data—Note 20. Legal Proceedings and Contingencies” and is incorporated by reference herein.

The opening of Item 3, Legal Proceedings.22

Sources

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    Wikidata and SEC EDGARDeepak L. Bhatt, Board member
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