BRISTOL MYERS SQUIBB CO
For the period ended Dec 31, 2023. Filed Feb 13, 2024.
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FY2023 · Filed Feb 13, 2024
BMY$62.140.0%Stored close · as of Nov 9, 2026
Extracted filing text, with the paragraph anchors used by the comparison.
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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. | ||
The text of this filing, as the company filed it with the SEC, without its images or exhibits. This is not investment advice.