Item 6. EXHIBITS
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Item 6. EXHIBITS
Exhibits (listed by number corresponding to the Exhibit Table of Item 601 in Regulation S-K). The Exhibits designated by the symbol ‡‡ are management contracts or compensatory plans or arrangements.
| Exhibit No. | Description | |||||||
| ‡‡10a | Bristol-Myers Squibb Company 2026 Stock Award and Incentive Plan (incorporated herein by reference to Exhibit B to Bristol-Myers Squibb Company’s Definitive Proxy Statement filed on March 25, 2026). | |||||||
| 22 | Subsidiary Issuers of Guarantee Securities (incorporated by reference to Exhibit 22 of Bristol Myers Squibb Company's Annual Report on Form 10-K filed on February 11, 2026) | |||||||
| 31a. | Section 302 Certification Letter (filed herewith). | |||||||
| 31b. | Section 302 Certification Letter (filed herewith). | |||||||
| 32a. | Section 906 Certification Letter (furnished herewith). | |||||||
| 32b. | Section 906 Certification Letter (furnished herewith). | |||||||
| 101.INS | Inline XBRL Instance Document - the instance document does not appear in the Interactive Data File because its XBRL tags are embedded within the Inline XBRL document. | |||||||
| 101.SCH | Inline XBRL Taxonomy Extension Schema Document. | |||||||
| 101.CAL | Inline XBRL Taxonomy Extension Calculation Linkbase Document. | |||||||
| 101.DEF | Inline XBRL Taxonomy Extension Definition Linkbase Document. | |||||||
| 101.LAB | Inline XBRL Taxonomy Extension Label Linkbase Document. | |||||||
| 101.PRE | Inline XBRL Taxonomy Extension Presentation Linkbase Document. | |||||||
| 104 | Cover Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101). |
- Indicates, in this Quarterly Report on Form 10-Q, brand names of products, which are registered trademarks not solely owned by the Company or its subsidiaries. Keytruda and Winrevair are trademarks of Merck & Co., Inc., Rahway, NJ, USA; Plavix is a trademark of Sanofi; and Tecentriq is a trademark of Genentech, Inc. Brand names of products that are in all italicized letters, without an asterisk, are registered trademarks of BMS and/or one of its subsidiaries.
SUMMARY OF ABBREVIATED TERMS
Bristol-Myers Squibb Company and its consolidated subsidiaries may be referred to as Bristol Myers Squibb, BMS, the Company, we, our or us in this Quarterly Report on Form 10-Q, unless the context otherwise indicates. Throughout this Quarterly Report on Form 10-Q we have used terms which are defined below:
| 2025 Form 10-K | Annual Report on Form 10-K for the fiscal year ended December 31, 2025 | Merck | Merck & Co., Inc., Rahway, NJ, USA | ||||||||
| 2seventy bio | 2seventy bio, Inc. | MF | myelofibrosis | ||||||||
| ANDA | Abbreviated New Drug Application | Mirati | Mirati Therapeutics, Inc. | ||||||||
| AstraZeneca | AstraZeneca PLC | MZL | marginal zone lymphoma | ||||||||
| AOCL | Accumulated other comprehensive loss | NDA | New Drug Application | ||||||||
| BioArctic | BioArctic AB | NHL | Non-Hodgkin's Lymphoma | ||||||||
| BioNTech | BioNTech SE | oHCM | Obstructive Hypertrophic Cardiomyopathy | ||||||||
| Celgene | Celgene Corporation | Ono | Ono Pharmaceutical Co., Ltd | ||||||||
| CERCLA | U.S. Comprehensive Environmental Response, Compensation and Liability Act | PD-1 | programmed cell death protein 1 | ||||||||
| cHL | classical Hodgkins Lymphoma | PD-L1 | programmed death-ligand 1 | ||||||||
| CRC | colorectal cancer | PDUFA | Prescription Drug User Fee Act | ||||||||
| CVR | Contingent value right | Pfizer | Pfizer, Inc. | ||||||||
| Dr. Reddy's Laboratories | Dr. Reddy’s Laboratories, Limited and Dr. Reddy’s Laboratories, Inc. | PFS | progression-free survival | ||||||||
| EC | European Commission | PsA | psoriatic arthritis | ||||||||
| EPS | earnings per share | Quarterly Report on Form 10-Q | Quarterly Report on Form 10-Q for the quarter ended June 30, 2026 | ||||||||
| ESCC | esophageal squamous cell carcinoma | R&D | research and development | ||||||||
| EU | European Union | RDFV | readily determinable fair values | ||||||||
| Evotec | Evotec SE | REMS | risk evaluation and mitigation strategy | ||||||||
| Exchange Act | the Securities Exchange Act of 1934 | Roche | F. Hoffman-La Roche & Co. | ||||||||
| FASB | Financial Accounting Standards Board | RRMM | relapsed or refractory multiple myeloma | ||||||||
| FDA | U.S. Food and Drug Administration | Sanofi | Sanofi S.A. | ||||||||
| GAAP | generally accepted accounting principles | SAR | Special Administrative Region | ||||||||
| GTN | gross-to-net | SEC | U.S. Securities and Exchange Commission | ||||||||
| HCM | hypertrophic cardiomyopathy | sNDA | supplemental New Drug Application | ||||||||
| Hengrui | Jiangsu Hengrui Pharmaceuticals Co., Ltd. | SPC | Supplementary Protection Certificate | ||||||||
| HHS | Health and Human Services | SystImmune | SystImmune, Inc. | ||||||||
| IPRD | in-process research and development | TNBC | triple negative breast cancer | ||||||||
| IRA | Inflation Reduction Act of 2022 | UK | United Kingdom | ||||||||
| IRS | Internal Revenue Service | U.S. | United States | ||||||||
| IT | Information Technology | VAT | value added tax | ||||||||
| MCL | mantle cell lymphoma | VEGF-A | Vascular endothelial growth factor A | ||||||||
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.
| BRISTOL-MYERS SQUIBB COMPANY (REGISTRANT) | |||||||||||
| Date: | July 30, 2026 | By: | /s/ Christopher Boerner, Ph.D. | ||||||||
| Christopher Boerner, Ph.D. Chair of the Board and Chief Executive Officer | |||||||||||
| Date: | July 30, 2026 | By: | /s/ David V. Elkins | ||||||||
| David V. Elkins Chief Financial Officer |
Previous: Item 5. OTHER INFORMATION