Item 16. FORM 10-K SUMMARY.
65K characters. Original on sec.gov ·
Item 16. FORM 10-K SUMMARY.
None.
SIGNATURES
Pursuant to the requirements of Section 13 or 15(d) 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) | ||||||||
| By | /s/ CHRISTOPHER BOERNER, Ph.D. | |||||||
| Christopher Boerner, Ph.D. | ||||||||
| Chief Executive Officer | ||||||||
| Date: February 13, 2024 |
Pursuant to the requirements of the Securities Exchange Act of 1934, this Report has been signed below by the following persons on behalf of the Registrant and in the capacities and on the dates indicated.
| Signature | Title | Date | ||||||||||||
| /s/ CHRISTOPHER BOERNER, Ph.D. | Chief Executive Officer | February 13, 2024 | ||||||||||||
| (Christopher Boerner, Ph.D.) | (Principal Executive Officer) | |||||||||||||
| /s/ DAVID V. ELKINS | Chief Financial Officer | February 13, 2024 | ||||||||||||
| (David V. Elkins) | (Principal Financial Officer) | |||||||||||||
| /s/ SHARON GREENLEES | Senior Vice President and Corporate Controller | February 13, 2024 | ||||||||||||
| (Sharon Greenlees) | (Principal Accounting Officer) | |||||||||||||
| /s/ GIOVANNI CAFORIO, M.D. | Executive Chairman of the Board | February 13, 2024 | ||||||||||||
| (Giovanni Caforio, M.D.) | ||||||||||||||
| /s/ PETER J. ARDUINI | Director | February 13, 2024 | ||||||||||||
| (Peter J. Arduini) | ||||||||||||||
| /s/ DEEPAK L. BHATT. M.D. MPH | Director | February 13, 2024 | ||||||||||||
| (Deepak L. Bhatt, M.D. MPH) | ||||||||||||||
| /s/ JULIA A. HALLER, M.D. | Director | February 13, 2024 | ||||||||||||
| (Julia A. Haller, M.D.) | ||||||||||||||
| /s/ MANUEL HIDALGO MEDINA, M.D., Ph.D. | Director | February 13, 2024 | ||||||||||||
| (Manuel Hidalgo Medina, M.D., Ph.D.) | ||||||||||||||
| /s/ PAULA A. PRICE | Director | February 13, 2024 | ||||||||||||
| (Paula A. Price) | ||||||||||||||
| /s/ DERICA W. RICE | Director | February 13, 2024 | ||||||||||||
| (Derica W. Rice) | ||||||||||||||
| /s/ THEODORE R. SAMUELS | Director | February 13, 2024 | ||||||||||||
| (Theodore R. Samuels) | ||||||||||||||
| /s/ GERALD L. STORCH | Director | February 13, 2024 | ||||||||||||
| (Gerald L. Storch) | ||||||||||||||
| /s/ KAREN H. VOUSDEN, Ph.D. | Director | February 13, 2024 | ||||||||||||
| (Karen H. Vousden, Ph.D.) | ||||||||||||||
| /s/ PHYLLIS R. YALE | Director | February 13, 2024 | ||||||||||||
| (Phyllis R. Yale) |
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 2023 Form 10-K, unless the context otherwise indicates. Throughout this 2023 Form 10-K, we have used terms which are defined below:
| 2023 Form 10-K | Annual Report on Form 10-K for the fiscal year ended December 31, 2023 | MAA | Marketing Authorization Application | ||||||||
| 2021 Plan | 2021 Stock Award and Incentive Plan | MCOs | Managed Care Organizations | ||||||||
| 2seventy bio | 2seventy bio, Inc. | MDL | multi-district litigation | ||||||||
| 340B Program | 340B Drug Pricing Program | MDS | myelodysplastic syndromes | ||||||||
| AbbVie | AbbVie Inc. | MF | myelofibrosis | ||||||||
| Agenus | Agenus Inc. | MPM | Malignant Pleural Mesothelioma | ||||||||
| aGVHD | acute graft-versus-host disease | MSI-H | high microsatellite instability | ||||||||
| Amgen | Amgen Inc. | Mead Johnson | Mead Johnson Nutrition Company | ||||||||
| Amylin | Amylin Pharmaceuticals, Inc. | Merck | Merck & Co., Inc. | ||||||||
| ANDA | abbreviated New Drug Application | Mirati | Mirati Therapeutics, Inc. | ||||||||
| AstraZeneca | AstraZeneca PLC | MyoKardia | MyoKardia, Inc. | ||||||||
| ASC | Accounting Standards Codification | NAV | net asset value | ||||||||
| ASR | Accelerated Share Repurchase | NDA | New Drug Application | ||||||||
| BCMA | B-cell maturation antigen | NKT | natural killer T | ||||||||
| Biogen | Biogen, Inc. | Nimbus | Nimbus Therapeutics, LLC | ||||||||
| Biohaven | Biohaven Pharmaceutical Holding Company Ltd. | Novartis | Novartis Pharmaceutical Corporation | ||||||||
| BLA | Biologics License Application | NSCLC | non-small cell lung cancer | ||||||||
| BridgeBio | BridgeBio Pharma Inc. | NVAF | non-valvular atrial fibrillation | ||||||||
| CAR-T | Chimeric Antigen Receptor T cells | OCE | Oncology Center of Excellence | ||||||||
| Celgene | Celgene Corporation acquired by BMS on November 20, 2019 | OECD | Organization for Economic Co-operation and Development | ||||||||
| CERCLA | U.S. Comprehensive Environmental Response, Compensation and Liability Act | OIG | Office of Inspector General of the U.S. Department of Health and Human Services | ||||||||
| cGMP | current Good Manufacturing Practices | Orum | Orum Therapeutics | ||||||||
| Cheplapharm | Cheplapharm Arzneimittel GmbH | OTC | over-the-counter | ||||||||
| CHMP | Committee for Medicinal Products for Human Use | Ono | Ono Pharmaceutical Co., Ltd. | ||||||||
| CML | chronic myeloid leukemia | Otsuka | Otsuka Pharmaceutical Co., Ltd. | ||||||||
| CLL | Chronic lymphocytic leukemia | PBMs | Pharmacy Benefit Managers | ||||||||
| COSO | Committee of Sponsoring Organizations of the Treadway Commission | PBRGs | People and Business Resource Groups | ||||||||
| CRC | colorectal cancer | PCAOB | Public Company Accounting Oversight Board | ||||||||
| DMC | Data Monitoring Committee | PD-1 | programmed death receptor-1 | ||||||||
| Dragonfly | Dragonfly Therapeutics, Inc. | PDMA | Prescription Drug Marketing Act | ||||||||
| DSA | Distribution Services Agreement | PDUFA | Prescription Drug User Fee Act | ||||||||
| EC | European Commission | Pfizer | Pfizer, Inc. | ||||||||
| EGFR | estimated glomerular filtration rate | Prothena | Prothena Corporation | ||||||||
| Eisai | Eisai Co., Ltd. | PhRMA Code | Pharmaceutical Research and Manufacturers of America’s Professional Practices Code | ||||||||
| EMA | European Medicines Agency | PRP | potentially responsible party | ||||||||
| EPO | European Patent Office | PsA | psoriatic arthritis | ||||||||
| EPS | earnings per share | PTR | patent term restoration | ||||||||
| ESA | erythoropoiesis-stimulating agent | R&D | research and development | ||||||||
| Evotec | Evotec SE | RA | rheumatoid arthritis | ||||||||
| EU | except as otherwise noted, EU refers to the countries that are members of the European Union plus the United Kingdom | RayzeBio | RayzeBio, Inc. | ||||||||
| FASB | Financial Accounting Standards Board | RCC | renal cell carcinoma | ||||||||
| FDA | U.S. Food and Drug Administration | RDP | Regulatory Data Protection | ||||||||
| FL | follicular lymphoma | REMS | Risk Evaluation and Mitigation Strategy | ||||||||
| GAAP | U.S. generally accepted accounting principles | ROS1 | c-ros oncogene 1 | ||||||||
| Gilead | Gilead Sciences, Inc. | Roche | Roche Holding AG | ||||||||
| GILTI | global intangible low taxed income | Sanofi | Sanofi S.A. | ||||||||
| GlaxoSmithKline | GlaxoSmithKline PLC | sBLA | supplemental Biologics License Application | ||||||||
| GTN | gross-to-net | SEC | U.S. Securities and Exchange Commission | ||||||||
| Halozyme | Halozyme Therapeutics, Inc. | SLE | systemic lupus erythematosus | ||||||||
| HCM | hypertrophic cardiomyopathy | SOFR | Secured Overnight Financing Rate | ||||||||
| IMDC | International Metastatic Renal Cell Carcinoma Database Consortium | SPC | Supplementary Protection Certificate | ||||||||
| Immatics | Immatics N.V. | Takeda | Takeda Pharmaceutical Company Limited | ||||||||
| IO | immuno-oncology | TCJA | the Tax Cuts and Jobs Act of 2017 | ||||||||
| IPRD | in-process research and development | UC | ulcerative colitis | ||||||||
| IRS | Internal Revenue Services | U.S. | United States | ||||||||
| JIA | Juvenile Idiopathic Arthritis | UK | United Kingdom | ||||||||
| Lilly | Eli Lilly and Company | VAT | value added tax | ||||||||
| LOE | loss of exclusivity | WTO | World Trade Organization | ||||||||
| Karuna | Karuna Therapeutics, Inc. | ||||||||||
EXHIBIT INDEX
The Exhibits listed below are identified by numbers corresponding to the Exhibit Table of Item 601 of Regulation S-K. The Exhibits designated by the symbol ‡‡ are management contracts or compensatory plans or arrangements required to be filed pursuant to Item 15. The symbol ‡ in the Page column indicates that the Exhibit has been previously filed with the Commission and is incorporated herein by reference. Unless otherwise indicated, all Exhibits are part of Commission File Number 1-1136.
| † | Confidential treatment has been granted for certain portions which are omitted in the copy of the exhibit electronically filed with the Commission. |
| * | Indicates, in this 2023 Form 10-K, brand names of products, which are registered trademarks not solely owned by the Company or its subsidiaries. Abilify is a trademark of Otsuka Pharmaceutical Co., Ltd.; Cabometyx is a trademark of Exelixis, Inc.; Farxiga and Onglyza are trademarks of AstraZeneca AB; Gleevec is a trademark of Novartis AG; Keytruda is a trademark of Merck Sharp & Dohme Corp.; Otezla is a trademark of Amgen Inc.; 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. |
Previous: Item 15. EXHIBITS AND FINANCIAL STATEMENT SCHEDULE.