PRODUCT AND PIPELINE UPDATES
Entries organized by date and inclusive of first quarter and recent updates.
| Asset | Date
Announced | Milestone |
| CobenfyTM
(xanomeline and
trospium
chloride) | April 22 | The Phase 3 ARISE trial evaluating Cobenfy as an adjunctive treatment to atypical antipsychotics in adults with schizophrenia did not meet the threshold for statistical significance for the primary endpoint. |
| Camzyos®
(mavacamten) | April 17 | The U.S. Food and Drug Administration (FDA) updated the U.S. Prescribing Information for Camzyos, simplifying treatment options for patients and physicians by reducing the required echo monitoring for eligible patients in the maintenance phase and expanding patient eligibility by reducing contraindications. |
| Camzyos | April 14 | The Phase 3 ODYSSEY-HCM trial evaluating Camzyos for the treatment of adult patients with symptomatic New York Heart Association class II-III non-obstructive hypertrophic cardiomyopathy did not meet its dual primary endpoints. |
| Opdivo®
(nivolumab) +
Yervoy®
(ipilimumab) | April 11 | The FDA approved Opdivo plus Yervoy as a first-line treatment for adult patients with unresectable or metastatic hepatocellular carcinoma (HCC). |
| Opdivo + Yervoy | April 8 | The FDA approved Opdivo plus Yervoy as a first-line treatment of adult and pediatric patients (12 years and older) with unresectable or metastatic microsatellite instability-high or mismatch repair deficient colorectal cancer. |
| Opdivo | March 28 | The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) recommended approval of the perioperative regimen of Opdivo, in combination with platinum-based chemotherapy as neoadjuvant treatment, followed by Opdivo as monotherapy, as adjuvant treatment after surgical resection for the treatment of resectable non-small cell lung cancer at high risk of recurrence in adult patients whose tumors have PD-L1 expression ≥1%. |
| Subcutaneous
formulation of
Opdivo | March 28 | The CHMP of the EMA recommended approval of a new Opdivo formulation associated with a new route of administration (subcutaneous use), a new pharmaceutical form (solution for injection) and a new strength (600 mg/vial). |
| Breyanzi®
(lisocabtagene
maraleucel) | March 14 | The European Commission (EC) granted approval to Breyanzi for the treatment of adult patients with relapsed or refractory follicular lymphoma after two or more lines of systemic therapy. |
| Sotyktu®
(deucravacitinib) | March 8 | Announced positive data from the pivotal Phase 3 POETYK PsA-2 trial evaluating the efficacy and safety of Sotyktu in adults with active psoriatic arthritis. |
| Opdivo + Yervoy | March 7 | The EC approved Opdivo plus Yervoy for the first-line treatment of adult patients with unresectable or advanced HCC. |
| Opdivo | February 19 | Announced the final analysis of overall survival (OS) from the Phase 3 CheckMate -816 study. The results showed a statistically significant and clinically meaningful improvement in OS, a key secondary endpoint, compared to neoadjuvant chemotherapy alone. |
| Sotyktu | February 16 | Announced new five-year results from the POETYK PSO long-term extension trial of Sotyktu treatment in adult patients with moderate-to-severe plaque psoriasis. The safety profile of Sotyktu remained consistent through five years with no new safety signals identified. |
| OpdualagTM
(nivolumab and
relatlimab-rmbw) | February 13 | The Phase 3 RELATIVITY-098 trial evaluating Opdualag for the adjuvant treatment of patients with completely resected stage III-IV melanoma did not meet its primary endpoint of recurrence-free survival. |
| Breyanzi | February 10 | Announced positive topline results from the Phase 2 TRANSCEND FL trial evaluating Breyanzi in adult patients with relapsed or refractory marginal zone lymphoma. The trial cohort met its primary endpoint of overall response rate and key secondary endpoint of complete response rate. |
Financial Guidance
Bristol Myers Squibb is raising key 2025 non-GAAP line-item guidance assumptions as outlined below.
The company is increasing its full-year revenue guidance from approximately $45.5 billion to a range of approximately $45.8 billion to $46.8 billion, reflecting the strong performance of the Growth Portfolio, better-than-expected Legacy Portfolio sales in the first quarter of 2025, and a favorable impact of approximately $500 million related to foreign exchange rates.
In addition, full-year operating expense expectations remain approximately $16 billion, with an additional $200 million foreign exchange impact. The company now anticipates other income and expense in 2025 to be approximately $100 million of income due to higher-than-expected royalties and favorable interest income.
As a result of these changes, the company is raising the midpoint of its 2025 non-GAAP EPS guidance by $0.15 per share to an expected range of $6.70 to $7.00.
The stated guidance revisions include the estimated impact of current tariffs on U.S. products shipped to China, but do not account for any potential pharmaceutical sector tariffs.
| | Non-GAAP2,3 |
| February
(Prior) | April
(Updated) |
| Total Revenues (Reported & Ex-FX) | ~$45.5 billion | ~$45.8 - $46.8 billion |
| Gross Margin % | ~72% | No change |
| Operating Expenses1 | ~$16 billion | ~$16.2 billion |
| Other income/(expense) | ~$30 million | ~$100 million |
| Effective tax rate | ~18% | No change |
| Diluted EPS | $6.55-$6.85 | $6.70-$7.00 |
| 1 Operating Expenses = SG&A and R&D. |
| 2 See "Use of Non-GAAP Financial Information." |
| 3 February was calculated using foreign exchange rates as of January 9, 2025, and April was calculated using foreign exchange rates as of April 23, 2025. |
The 2025 financial guidance excludes the impact of any potential future strategic acquisitions, divestitures, specified items that have not yet been identified and quantified, and the impact of future Acquired IPRD charges and licensing income. To the extent we have quantified the impact of significant R&D charges or other income resulting from upfront or contingent milestone payments in connection with asset acquisitions or licensing of third-party intellectual property rights, we may update this information from time to time on our website www.bms.com, in the "Investors" section. Non-GAAP guidance assumes exchange rates as of the date noted. The financial guidance is subject to risks and uncertainties applicable to all forward-looking statements as described elsewhere in this press release.
A reconciliation of forward-looking non-GAAP measures, including non-GAAP EPS, to the most directly comparable GAAP measures is not provided because comparable GAAP measures for such measures are not reasonably accessible or reliable due to the inherent difficulty in forecasting and quantifying measures that would be necessary for such reconciliation. Namely, we are not, without unreasonable effort, able to reliably predict the impact of accelerated depreciation and impairment charges, legal and other settlements, gains and losses from equity investments and other adjustments. In addition, the company believes such a reconciliation would imply a degree of precision and certainty that could be confusing to investors. These items are uncertain, depend on various factors and may have a material impact on our future GAAP results. See "Cautionary Statement Regarding Forward-Looking Statements" and "Use of Non-GAAP Financial Information."
Conference Call Information
Bristol Myers Squibb will host a conference call today, Thursday, April 24, 2025, at 8:00 a.m. ET, during which company executives will review financial results with the investment community.
Investors and the general public are invited to listen to a live webcast of the call at http://investor.bms.com. Materials related to the call will be available at ...http://investor.bms.com prior to the start of the conference call.
A replay of the webcast will be available at http://investor.bms.com approximately three hours after the conference call concludes.
About Bristol Myers Squibb: Transforming Patients' Lives Through Science
At Bristol Myers Squibb, our mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. We are pursuing bold science to define what's possible for the future of medicine and the patients we serve. For more information, visit us at BMS.com and follow us on LinkedIn, X, YouTube, Facebook and Instagram.
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Use of Non-GAAP Financial Information
In discussing financial results and guidance, the company refers to financial measures that are not in accordance with U.S. Generally Accepted Accounting Principles (GAAP). The non-GAAP financial measures are provided as supplemental information to the financial measures presented in this press release that are calculated and presented in accordance with GAAP and are presented because management has evaluated the company’s financial results both including and excluding the adjusted items or the effects of foreign currency translation, as applicable, and believes that the non-GAAP financial measures presented portray the results of the company's baseline performance, supplement or enhance management's, analysts' and investors' overall understanding of the company’s underlying financial performance and trends and facilitate comparisons among current, past and future periods. In addition, non-GAAP gross margin, which is gross profit excluding certain specified items, as a percentage of revenues, non-GAAP operating margin, which is gross profit less selling, general and administrative expenses and research and development expenses excluding certain specified items as a percentage of revenues, non-GAAP operating expenses, which is selling, general and administrative and research and development expenses excluding certain specified items, non-GAAP selling, general and administrative expenses, which is selling, general and administrative expenses excluding certain specified items, and non-GAAP research and development expenses, which is research and development expenses excluding certain specified items, are relevant and useful for investors because they allow investors to view performance in a manner similar to the method used by our management and make it easier for investors, analysts and peers to compare our operating performance to other companies in our industry and to compare our year-over-year results.
This earnings release and the accompanying tables also provide certain revenues and expenses, as well as non-GAAP measures, excluding the impact of foreign exchange ("Ex-Fx"). We calculate foreign exchange impacts by converting our current-period local currency financial results using the prior period average currency rates and comparing these adjusted amounts to our current-period results. Ex-Fx financial measures are not accounted for according to GAAP because they remove the effects of currency movements from GAAP results.
Non-GAAP financial measures such as non-GAAP earnings and related EPS information are adjusted to exclude certain costs, expenses, gains and losses and other specified items that are evaluated on an individual basis after considering their quantitative and qualitative aspects and typically have one or more of the following characteristics, such as being highly variable, difficult to project, unusual in nature, significant to the results of a particular period or not indicative of past or future operating results. These items are excluded from non-GAAP earnings and related EPS information because the company believes they neither relate to the ordinary course of the company’s business nor reflect the company’s underlying business performance. Similar charges or gains were recognized in prior periods and will likely reoccur in future periods, including amortization of acquired intangible assets, including product rights that generate a significant portion of our ongoing revenue and will recur until the intangible assets are fully amortized, unwinding of inventory purchase price adjustments, acquisition and integration expenses, restructuring costs, accelerated depreciation and impairment of property, plant and equipment and intangible assets, divestiture gains or losses, stock compensation resulting from acquisition-related equity awards, pension, legal and other contractual settlement charges, equity investment and contingent value rights fair value adjustments (including fair value adjustments attributed to limited partnership equity method investments), and amortization of fair value adjustments of debt acquired from Celgene in our 2019 exchange offer, among other items. Deferred and current income taxes attributed to these items are also adjusted for considering their individual impact to the overall tax expense, deductibility and jurisdictional tax rates.
Because the non-GAAP financial measures are not calculated in accordance with GAAP, they should not be considered superior to and are not intended to be considered in isolation or as a substitute for the related financial measures presented in the press release that are prepared in accordance with GAAP and may not be the same as or comparable to similarly titled measures presented by other companies due to possible differences in method and in the items being adjusted. We encourage investors to review our financial statements and publicly-filed reports in their entirety and not to rely on any single financial measure.
Reconciliations of the non-GAAP financial measures to the most comparable GAAP measures are provided in the accompanying financial tables and will also be available on the company’s website at www.bms.com. Within the accompanying financial tables presented, certain columns and rows may not add due to the use of rounded numbers. Percentages and EPS amounts presented are calculated from the underlying amounts.
A reconciliation of forward-looking non-GAAP measures, including non-GAAP EPS, to the most directly comparable GAAP measures is not provided because comparable GAAP measures for such measures are not reasonably accessible or reliable due to the inherent difficulty in forecasting and quantifying measures that would be necessary for such reconciliation. Namely, we are not, without unreasonable effort, able to reliably predict the impact of accelerated depreciation and impairment charges, legal and other settlements, gains and losses from equity investments and other adjustments. In addition, the company believes such a reconciliation would imply a degree of precision and certainty that could be confusing to investors. These items are uncertain, depend on various factors and may have a material impact on our future GAAP results.
Website Information
We routinely post important information for investors on our website, BMS.com, in the "Investors" section. We may use this website as a means of disclosing material, non-public information and for complying with our disclosure obligations under Regulation FD. Accordingly, investors should monitor the Investors section of our website, in addition to following our press releases, Securities and Exchange Commission (SEC) filings, public conference calls, presentations and webcasts. We may also use social media channels to communicate with our investors and the public about our company, our products and other matters, and those communications could be deemed to be material information. The information contained on, or that may be accessed through, our website or social media channels are not incorporated by reference into, and are not a part of, this document.
Cautionary Statement Regarding Forward-Looking Statements
This earnings release and the related attachments (as well as the oral statements made with respect to information contained in this release and the attachments) contain certain "forward-looking" statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, regarding, among other things, the company’s 2025 financial guidance, its business development and capital allocation strategy, anticipated developments in the company’s pipeline, expectations with respect to the company’s future market position and the projected benefits of the company’s alliances and other business development activities. These statements may be identified by the fact that they use words such as "should," "could," "expect," "anticipate," "estimate," "target," "may," "project," "guidance," "intend," "plan," "believe," "will" and other words and terms of similar meaning and expression in connection with any discussion of future operating or financial performance, although not all forward-looking statements contain such terms. All statements that are not statements of historical facts are, or may be deemed to be, forward-looking statements. No forward-looking statement can be guaranteed, and there is no assurance that the company will achieve its financial guidance and long-term targets, that the company’s future clinical studies will support the data described in this release, that the company’s product candidates will receive necessary clinical and manufacturing regulatory approvals, that the company’s pipeline products will prove to be commercially successful, that clinical and manufacturing regulatory approvals will be sought or obtained within currently expected timeframes, or that contractual milestones will be achieved.
Forward-looking statements are based on current expectations and projections about the company’s future financial results, goals, plans and objectives and involve inherent risks, assumptions and uncertainties, including internal or external factors that could delay, divert or change any of them in the next several years, that are difficult to predict, may be beyond the company’s control and could cause the company’s future financial results, goals, plans and objectives to differ materially from those expressed in, or implied by, the statements. Such risks, uncertainties and other matters include, but are not limited to: increasing pricing pressures from market access, pharmaceutical pricing controls and discounting; market actions taken by private and government payers to manage drug utilization and contain costs; government actions relating to the imposition of new tariffs, trade restrictions and export regulations; the company’s ability to retain patent and market exclusivity for certain products; regulatory changes that result in lower prices, lower reimbursement rates and smaller populations for whom payers will reimburse; changes under the 340B Drug Pricing Program; the company’s ability to obtain and maintain regulatory approval for its product candidates; the possibility of difficulties and delays in product introduction and commercialization; increasing industry competition; potential difficulties, delays and disruptions in manufacturing, distribution or sale of products; the company’s ability to identify potential strategic acquisitions, licensing opportunities or other beneficial transactions; failure to complete, or delays in completing, collaborations, acquisitions, divestitures, alliances and other portfolio actions and the failure to achieve anticipated benefits from such transactions and actions; exposure to litigation and/or regulatory actions or investigations; the impact of any healthcare reform and legislation or regulatory action in the United States and international markets; increasing market penetration of lower-priced generic products; the failure of the company’s suppliers, vendors, outsourcing partners, alliance partners and other third parties to meet their contractual, regulatory and other obligations; the impact of counterfeit or unregistered versions of the company’s products and from stolen products; product label changes or other measures that could result in declining sales; safety or efficacy concerns regarding the company’s products or any product in the same class as the company’s products; the risk of cyber-attacks and unauthorized disclosure of trade secrets or other confidential data; the company’s ability to execute its financial, strategic and operational plans; the company’s ability to attract and retain key personnel; the impact of the company’s significant indebtedness; political and financial instability of international economies and sovereign risk; interest rate and currency exchange rate fluctuations, credit and foreign exchange risk management; risks relating to the use of social media platforms; issuance of new or revised accounting standards; and risks relating to public health outbreaks, epidemics and pandemics.
Forward-looking statements in this earnings release should be evaluated together with the many risks and uncertainties that affect the company’s business and market, particularly those identified in the cautionary statement and risk factors discussion in the company’s Annual Report on Form 10-K for the year ended December 31, 2024, as updated by the company’s subsequent Quarterly Reports on Form 10-Q, Current Reports on Form 8-K and other filings with the SEC. The forward-looking statements included in this document are made only as of the date of this document and except as otherwise required by applicable law, the company undertakes no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future events, changed circumstances or otherwise.
| BRISTOL-MYERS SQUIBB COMPANY |
| CONSOLIDATED STATEMENTS OF EARNINGS |
| (Unaudited, dollars and shares in millions except per share data) |
| | |
| | Three Months Ended March
31, |
| | 2025 | | 2024 |
| | | | |
| Net product sales | $ | 10,886 | | | $ | 11,559 | |
| Alliance and other revenues | | 315 | | | | 306 | |
| Total Revenues | | 11,201 | | | | 11,865 | |
| | | | |
| Cost of products sold(a) | | 3,033 | | | | 2,932 | |
| Selling, general and administrative | | 1,584 | | | | 2,367 | |
| Research and development | | 2,257 | | | | 2,695 | |
| Acquired IPRD | | 188 | | | | 12,949 | |
| Amortization of acquired intangible assets | | 830 | | | | 2,357 | |
| Other (income)/expense, net | | 339 | | | | 81 | |
| Total Expenses | | 8,230 | | | | 23,381 | |
| | | | |
| Earnings/(Loss) Before Income Taxes | | 2,971 | | | | (11,516 | ) |
| Income tax provision | | 509 | | | | 392 | |
| Net Earnings/(Loss) | | 2,462 | | | | (11,908 | ) |
| Noncontrolling Interest | | 6 | | | | 3 | |
| Net Earnings/(Loss) Attributable to BMS | $ | 2,456 | | | $ | (11,911 | ) |
| | | | |
| Weighted-Average Common Shares Outstanding: | | | |
| Basic | | 2,031 | | | | 2,023 | |
| Diluted | | 2,040 | | | | 2,023 | |
| | | | |
| Earnings/(Loss) per Common Share: | | | |
| Basic | $ | 1.21 | | | $ | (5.89 | ) |
| Diluted | | 1.20 | | | | (5.89 | ) |
| | | | |
| Other (income)/expense, net | | | |
| Interest expense(b) | $ | 494 | | | $ | 425 | |
| Royalty income - divestitures | | (272 | ) | | | (271 | ) |
| Royalty and licensing income | | (259 | ) | | | (161 | ) |
| Provision for restructuring | | 133 | | | | 220 | |
| Investment income | | (138 | ) | | | (183 | ) |
| Integration expenses | | 41 | | | | 71 | |
| Litigation and other settlements | | 257 | | | | 2 | |
| Acquisition expense | | 2 | | | | 49 | |
| Equity investment (gains)/losses | | 78 | | | | (102 | ) |
| Other | | 3 | | | | 31 | |
| Other (income)/expense, net | $ | 339 | | | $ | 81 | |
| (a) Excludes amortization of acquired intangible assets. |
| (b) Includes amortization of purchase price adjustments to Celgene debt. |
| BRISTOL-MYERS SQUIBB COMPANY |
| PRODUCT REVENUES |
| FOR THE THREE MONTHS ENDED MARCH 31, 2025 AND 2024 |
| (Unaudited, dollars in millions) |
| | | | | | | | | | | | | | | |
| | | | | | | | | | | | | | | Change vs. 2024 |
| | | 2025 | | 2024 | | GAAP | | Excl. F/X** |
| | | U.S. | | Int'l(c) | | WW(d) | | U.S. | | Int'l(c) | | WW(d) | | U.S. | | Int'l(c) | | WW(d) | | U.S. | | Int'l(c) | | WW(d) |
| Growth Portfolio | | | | | | | | | | | | | | | | | | | | | | | | |
| Opdivo | | $ | 1,332 | | $ | 933 | | $ | 2,265 | | $ | 1,155 | | $ | 923 | | $ | 2,078 | | 15% | | 1% | | 9% | | 15% | | 7% | | 12% |
| Opdivo Qvantig | | | 8 | | | — | | | 9 | | | — | | | — | | | — | | N/A | | N/A | | N/A | | N/A | | N/A | | N/A |
| Orencia | | | 555 | | | 215 | | | 770 | | | 572 | | | 226 | | | 798 | | (3)% | | (5)% | | (4)% | | (3)% | | (1)% | | (2)% |
| Yervoy | | | 394 | | | 230 | | | 624 | | | 368 | | | 215 | | | 583 | | 7% | | 7% | | 7% | | 7% | | 12% | | 9% |
| Reblozyl | | | 390 | | | 89 | | | 478 | | | 293 | | | 61 | | | 354 | | 33% | | 44% | | 35% | | 33% | | 49% | | 36% |
| Opdualag | | | 228 | | | 25 | | | 252 | | | 198 | | | 8 | | | 206 | | 15% | | >200% | | 23% | | 15% | | >200% | | 23% |
| Breyanzi | | | 204 | | | 60 | | | 263 | | | 87 | | | 20 | | | 107 | | 133% | | >200% | | 146% | | 133% | | >200% | | 148% |
| Camzyos | | | 126 | | | 33 | | | 159 | | | 77 | | | 7 | | | 84 | | 63% | | >200% | | 89% | | 63% | | >200% | | 90% |
| Zeposia | | | 61 | | | 46 | | | 107 | | | 72 | | | 38 | | | 110 | | (16)% | | 22% | | (3)% | | (16)% | | 26% | | (2)% |
| Abecma | | | 59 | | | 45 | | | 103 | | | 52 | | | 30 | | | 82 | | 13% | | 47% | | 26% | | 13% | | 54% | | 28% |
| Sotyktu | | | 32 | | | 23 | | | 55 | | | 34 | | | 10 | | | 44 | | (5)% | | 138% | | 27% | | (5)% | | 146% | | 29% |
| Krazati | | | 44 | | | 4 | | | 48 | | | 21 | | | — | | | 21 | | 116% | | >200% | | 125% | | 116% | | >200% | | 125% |
| Cobenfy | | | 27 | | | — | | | 27 | | | — | | | — | | | — | | N/A | | N/A | | N/A | | N/A | | N/A | | N/A |
| Other Growth Products(a) | | | 174 | | | 229 | | | 403 | | | 154 | | | 171 | | | 325 | | 13% | | 34% | | 24% | | 13% | | 35% | | 25% |
| Total Growth Portfolio | | | 3,633 | | | 1,930 | | | 5,563 | | | 3,083 | | | 1,709 | | | 4,792 | | 18% | | 13% | | 16% | | 18% | | 18% | | 18% |
| Legacy Portfolio | | | | | | | | | | | | | | | | | | | | | | | | |
| Eliquis | | | 2,646 | | | 919 | | | 3,565 | | | 2,821 | | | 899 | | | 3,720 | | (6)% | | 2% | | (4)% | | (6)% | | 5% | | (3)% |
| Revlimid | | | 809 | | | 127 | | | 936 | | | 1,453 | | | 216 | | | 1,669 | | (44)% | | (41)% | | (44)% | | (44)% | | (39)% | | (44)% |
| Pomalyst/Imnovid | | | 537 | | | 122 | | | 658 | | | 597 | | | 268 | | | 865 | | (10)% | | (55)% | | (24)% | | (10)% | | (53)% | | (24)% |
| Sprycel | | | 126 | | | 49 | | | 175 | | | 282 | | | 92 | | | 374 | | (56)% | | (47)% | | (53)% | | (56)% | | (43)% | | (53)% |
| Abraxane | | | 40 | | | 65 | | | 105 | | | 145 | | | 72 | | | 217 | | (72)% | | (10)% | | (52)% | | (72)% | | (6)% | | (50)% |
| Other Legacy Products(b) | | | 82 | | | 116 | | | 199 | | | 95 | | | 133 | | | 228 | | (14)% | | (10)% | | (12)% | | (14)% | | (8)% | | (11)% |
| Total Legacy Portfolio | | | 4,240 | | | 1,398 | | | 5,638 | | | 5,393 | | | 1,680 | | | 7,073 | | (21)% | | (17)% | | (20)% | | (21)% | | (14)% | | (20)% |
| Total Revenues | | $ | 7,873 | | $ | 3,328 | | $ | 11,201 | | $ | 8,476 | | $ | 3,389 | | $ | 11,865 | | (7)% | | (2)% | | (6)% | | (7)% | | 2% | | (4)% |
| ** | | See "Use of Non-GAAP Financial Information". |
| (a) | | Includes Augtyro, Onureg, Inrebic, Nulojix, Empliciti and royalty revenues. |
| (b) | | Includes other mature brands. |
| (c) | | Includes Puerto Rico. |
| (d) | | Worldwide (WW) includes U.S. and International (Int'l). |
| BRISTOL-MYERS SQUIBB COMPANY |
| INTERNATIONAL REVENUES(a) |
| FOREIGN EXCHANGE IMPACT (%) |
| (Unaudited) |
| | |
| | Three Months Ended March 31, 2025 |
| | Revenue
Change % | | F/X %
Favorable/
(Unfavorable)
** | | Revenue
Change %
Ex- F/X ** |
| Growth Portfolio | | | | | |
| Opdivo | 1% | | (6)% | | 7% |
| Opdivo Qvantig | N/A | | N/A | | N/A |
| Orencia | (5)% | | (4)% | | (1)% |
| Yervoy | 7% | | (6)% | | 12% |
| Reblozyl | 44% | | (5)% | | 49% |
| Opdualag | >200% | | NM | | >200% |
| Breyanzi | >200% | | NM | | >200% |
| Camzyos | >200% | | NM | | >200% |
| Zeposia | 22% | | (4)% | | 26% |
| Abecma | 47% | | (6)% | | 54% |
| Sotyktu | 138% | | (9)% | | 146% |
| Krazati | >200% | | NM | | >200% |
| Cobenfy | N/A | | N/A | | N/A |
| Other Growth Products(b) | 34% | | (1)% | | 35% |
| Total Growth Portfolio | 13% | | (5)% | | 18% |
| Legacy Portfolio | | | | | |
| Eliquis | 2% | | (3)% | | 5% |
| Revlimid | (41)% | | (3)% | | (39)% |
| Pomalyst/Imnovid | (55)% | | (1)% | | (53)% |
| Sprycel | (47)% | | (3)% | | (43)% |
| Abraxane | (10)% | | (4)% | | (6)% |
| Other Legacy Products(c) | (10)% | | (2)% | | (8)% |
| Total Legacy Portfolio | (17)% | | (3)% | | (14)% |
| Total Revenues | (2)% | | (4)% | | 2% |
| NM | | Not meaningful |
| ** | | See "Use of Non-GAAP Financial Information". |
| (a) | | Includes Puerto Rico. |
| (b) | | Includes Augtyro, Onureg, Inrebic, Nulojix, Empliciti and royalty revenues. |
| (c) | | Includes other mature brands. |
| BRISTOL-MYERS SQUIBB COMPANY |
| WORLDWIDE REVENUES(a) |
| FOREIGN EXCHANGE IMPACT (%) |
| (Unaudited) |
| | |
| | Three Months Ended March 31, 2025 |
| | Revenue
Change % | | F/X %
Favorable/
(Unfavorable) ** | | Revenue
Change % Ex-
F/X ** |
| Growth Portfolio | | | | | |
| Opdivo | 9% | | (3)% | | 12% |
| Opdivo Qvantig | N/A | | N/A | | N/A |
| Orencia | (4)% | | (1)% | | (2)% |
| Yervoy | 7% | | (2)% | | 9% |
| Reblozyl | 35% | | (1)% | | 36% |
| Opdualag | 23% | | —% | | 23% |
| Breyanzi | 146% | | (2)% | | 148% |
| Camzyos | 89% | | (1)% | | 90% |
| Zeposia | (3)% | | (1)% | | (2)% |
| Abecma | 26% | | (2)% | | 28% |
| Sotyktu | 27% | | (2)% | | 29% |
| Krazati | 125% | | —% | | 125% |
| Cobenfy | N/A | | N/A | | N/A |
| Other Growth Products(b) | 24% | | (1)% | | 25% |
| Total Growth Portfolio | 16% | | (2)% | | 18% |
| Legacy Portfolio | | | | | |
| Eliquis | (4)% | | (1)% | | (3)% |
| Revlimid | (44)% | | —% | | (44)% |
| Pomalyst/Imnovid | (24)% | | —% | | (24)% |
| Sprycel | (53)% | | (1)% | | (53)% |
| Abraxane | (52)% | | (1)% | | (50)% |
| Other Legacy Products(c) | (12)% | | (1)% | | (11)% |
| Total Legacy Portfolio | (20)% | | (1)% | | (20)% |
| Total Revenues | (6)% | | (1)% | | (4)% |
| NM | | Not meaningful |
| ** | | See "Use of Non-GAAP Financial Information". |
| (a) | | Worldwide (WW) includes U.S. and International (Int'l). |
| (b) | | Includes Augtyro, Onureg, Inrebic, Nulojix, Empliciti and royalty revenues. |
| (c) | | Includes other mature brands. |
| BRISTOL-MYERS SQUIBB COMPANY |
| RECONCILIATION OF GAAP AND NON-GAAP GROWTH DOLLARS AND PERCENTAGES EXCLUDING FOREIGN EXCHANGE IMPACT * |
| (Unaudited, dollars in millions) |
| | | | | | | | | | | | | | | | |
| THREE MONTHS | 2025 | | 2024 | | Change $ | | Change % | | Favorable /
(Unfavorable)
F/X $ ** | | 2025
Excl. F/X
** | | Favorable /
(Unfavorable)
F/X % ** | | % Change
Excl. F/X
** |
| Revenues | $ | 11,201 | | | $ | 11,865 | | | $ | (664) | | (6)% | | $ | (137) | | $ | 11,338 | | (1)% | | (4)% |
| Gross profit | | 8,168 | | | | 8,933 | | | | (764) | | (9)% | | | N/A | | | N/A | | N/A | | N/A |
| Gross profit excluding specified items(a) | | 8,183 | | | | 8,955 | | | | (772) | | (9)% | | | N/A | | | N/A | | N/A | | N/A |
| | | | | | | | | | | | | | | | |
| Gross margin(b) | | 72.9 | % | | | 75.3 | % | | | | | | | | | | | | |
| Gross margin excluding specified items(a) | | 73.1 | % | | | 75.5 | % | | | | | | | | | | | | |
| | | | | | | | | | | | | | | | |
| Selling, general and administrative | | 1,584 | | | | 2,367 | | | | (782) | | (33)% | | | 15 | | | 1,600 | | 1% | | (32)% |
| Selling, general and administrative excluding specified items(a) | | 1,583 | | | | 1,989 | | | | (405) | | (20)% | | | 15 | | | 1,598 | | 1% | | (20)% |
| | | | | | | | | | | | | | | | |
| Research and development | | 2,257 | | | | 2,695 | | | | (438) | | (16)% | | | 11 | | | 2,268 | | —% | | (16)% |
| Research and development excluding specified items(a) | | 2,235 | | | | 2,346 | | | | (112) | | (5)% | | | 11 | | | 2,246 | | —% | | (4)% |
| | | | | | | | | | | | | | | | |
| Operating margin(c) | | 38.6 | % | | | 32.6 | % | | | | | | | | | | | | |
| Operating margin excluding specified items | | 39.0 | % | | | 38.9 | % | | | | | | | | | | | | |
| * | | Foreign exchange impacts were derived by converting our current-period local currency financial results using the prior period average currency rates and comparing these adjusted amounts to our current-period results. |
| ** | | See "Use of Non-GAAP Financial Information". |
| (a) | | Refer to the Specified Items schedule below for further details. |
| (b) | | Represents gross profit as a percentage of Revenues. |
| (c) | | Operating margin represents gross profit less selling, general and administrative expenses and research and development expenses, as a percentage of Revenues. |
| BRISTOL-MYERS SQUIBB COMPANY |
| SPECIFIED ITEMS |
| (Unaudited, dollars in millions) |
| | |
| | Three Months Ended
March 31, 2025 |
| | 2025 | | 2024 |
| Inventory purchase price accounting adjustments | $ | 13 | | | $ | 8 | |
| Site exit and other costs | | 2 | | | | 14 | |
| Cost of products sold | | 14 | | | | 22 | |
| | | | |
| Acquisition related charges(a) | | — | | | | 372 | |
| Site exit and other costs | | 1 | | | | 6 | |
| Selling, general and administrative | | 1 | | | | 378 | |
| | | | |
| Acquisition related charges(a) | | — | | | | 348 | |
| Site exit and other costs | | 21 | | | | 1 | |
| Research and development | | 21 | | | | 349 | |
| | | | |
| Amortization of acquired intangible assets | | 830 | | | | 2,357 | |
| | | | |
| Interest expense(b) | | (12 | ) | | | (13 | ) |
| Provision for restructuring | | 133 | | | | 220 | |
| Integration expenses | | 41 | | | | 71 | |
| Litigation and other settlements | | 246 | | | | — | |
| Acquisition expenses | | 2 | | | | 49 | |
| Equity investment (gain)/losses | | 77 | | | | (102 | ) |
| Other | | 2 | | | | 10 | |
| Other (income)/expense, net | | 489 | | | | 235 | |
| | | | |
| Increase to Earnings before income taxes | | 1,356 | | | | 3,341 | |
| | | | |
| Income taxes on items above | | (143 | ) | | | (340 | ) |
| | | | |
| Increase to net earnings | $ | 1,212 | | | $ | 3,001 | |
| (a) | | Includes cash settlement of unvested stock awards, and other related costs incurred in connection with the recent acquisitions of Karuna, RayzeBio and Mirati. |
| (b) | | Includes amortization of purchase price adjustments to Celgene debt. |
| BRISTOL-MYERS SQUIBB COMPANY |
| RECONCILIATION OF CERTAIN GAAP LINE ITEMS TO CERTAIN NON-GAAP LINE ITEMS |
| (Unaudited, dollars and shares in millions except per share data) |
| | |
| | Three Months Ended March 31, 2025 |
| | GAAP | | Specified
Items(a) | | Non-GAAP |
| Gross profit | $ | 8,168 | | | $ | 14 | | | $ | 8,183 | |
| Selling, general and administrative | | 1,584 | | | | (1 | ) | | | 1,583 | |
| Research and development | | 2,257 | | | | (21 | ) | | | 2,235 | |
| Amortization of acquired intangible assets | | 830 | | | | (830 | ) | | | — | |
| Other (income)/expense, net | | 339 | | | | (489 | ) | | | (150 | ) |
| Earnings/(Loss) before income taxes | | 2,971 | | | | 1,356 | | | | 4,326 | |
| Income tax provision | | 509 | | | | 143 | | | | 652 | |
| Net earnings/(loss) attributable to BMS used for diluted EPS calculation | $ | 2,456 | | | $ | 1,212 | | | $ | 3,668 | |
| | | | | | |
| Weighted-average common shares outstanding—diluted | | 2,040 | | | | 2,040 | | | | 2,040 | |
| Diluted earnings/(loss) per share | $ | 1.20 | | | $ | 0.59 | | | $ | 1.80 | |
| | | | | | |
| Effective tax rate | | 17.1 | % | | | (2.1 | )% | | | 15.1 | % |
| | | | | | |
| | Three Months Ended March 31, 2024 |
| | GAAP | | Specified
Items(a) | | Non-GAAP |
| Gross profit | $ | 8,933 | | | $ | 22 | | | $ | 8,955 | |
| Selling, general and administrative | | 2,367 | | | | (378 | ) | | | 1,989 | |
| Research and development | | 2,695 | | | | (349 | ) | | | 2,346 | |
| Amortization of acquired intangible assets | | 2,357 | | | | (2,357 | ) | | | — | |
| Other (income)/expense, net | | 81 | | | | (235 | ) | | | (154 | ) |
| Earnings/(Loss) before income taxes | | (11,516 | ) | | | 3,341 | | | | (8,175 | ) |
| Income tax provision | | 392 | | | | 340 | | | | 732 | |
| Net earnings/(loss) attributable to BMS used for diluted EPS calculation | $ | (11,911 | ) | | $ | 3,001 | | | $ | (8,910 | ) |
| | | | | | |
| Weighted-average common shares outstanding—diluted | | 2,023 | | | | 2,023 | | | | 2,023 | |
| Diluted earnings/(loss) per share | $ | (5.89 | ) | | $ | 1.49 | | | $ | (4.40 | ) |
| | | | | | |
| Effective tax rate | | (3.4 | )% | | | (5.6 | )% | | | (9.0 | )% |
| (a) Refer to the Specified Items schedule above for further details. Effective tax rate on the Specified Items represents the difference between the GAAP and Non-GAAP effective tax rate. |
| BRISTOL-MYERS SQUIBB COMPANY |
| NET DEBT CALCULATION |
| AS OF MARCH 31, 2025 AND DECEMBER 31, 2024 |
| (Unaudited, dollars in millions) |
| | | | |
| | March 31,
2025 | | December 31,
2024 |
| | | | |
| Cash and cash equivalents | $ | 10,875 | | | $ | 10,346 | |
| Marketable debt securities - current | | 907 | | | | 513 | |
| Marketable debt securities - non-current | | 344 | | | | 320 | |
| Cash, cash equivalents and marketable debt securities | $ | 12,126 | | | $ | 11,179 | |
| Short-term debt obligations | | (3,554 | ) | | | (2,046 | ) |
| Long-term debt | | (46,157 | ) | | | (47,603 | ) |
| Net debt position | $ | (37,584 | ) | | $ | (38,470 | ) |
View source version on businesswire.com: https://www.businesswire.com/news/home/20250424015046/en/
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Investor Relations: investor.relations@bms.com
