Regeneron Reports Third Quarter 2026 Financial and Operating Results
Press Release Regeneron Reports Third Quarter 2026 Financial and Operating Results • Third quarter 2026 revenues increased 36% to $5.1 billion versus third quarter 2025
• Dupixent ® global net sales (recorded by Sanofi) increased 35% to $6.5 billion
• Expanded collaboration with Sanofi, adding multiple next-generation, long- acting immunology antibodies; $1.0 billion up-front to be recognized as collaboration revenue in fourth quarter 2026 with potential to receive up to an additional $7.0 billion in future milestones
• Pasatru ™ (garetosmab) approved by FDA for fibrodysplasia ossificans progressiva (FOP)
) today announced financial results for the third quarter of 2026 and provided a business update.
"This was an outstanding quarter for Regeneron, with Dupixent, EYLEA HD, and Libtayo each achieving record net sales," said Leonard S. Schleifer, M.D., Ph.D., Board co-Chair, President and Chief Executive Officer of Regeneron. "Our pipeline of about 50 product candidates is rapidly advancing. We expect an FDA decision for cemdisiran in generalized myasthenia gravis next month; our Phase 3 programs in multiple myeloma, lymphoma, anticoagulation, and obesity continue to advance; and we have generated encouraging early data in MASH, POTS, and ovarian cancer. Finally, we expanded our alliance with Sanofi to include four Regeneron- invented, next-generation, long-acting antibodies designed to build on the success of Dupixent."
"We are pleased with our third quarter financial results, which marked our third consecutive quarter of double-digit growth in both revenue and non-GAAP EPS," said Christopher Fenimore, Executive Vice President, Finance and Chief Financial Officer of Regeneron. "Strong commercial execution across our portfolio, together with the anticipated step-up in Sanofi collaboration revenue in the first full quarter following repayment of the Development Balance, drove a 36% increase in total revenues and a 70% increase in non-GAAP EPS, positioning us to deliver one of our strongest years ever." 1
Regeneron has approximately 50 product candidates in clinical development, including a number of marketed products for which it is investigating additional indications. Updates from the clinical pipeline include:
• In August 2026, the Ministry of Health, Labour and Welfare (MHLW) in Japan approved Libtayo as an adjuvant treatment for cutaneous squamous cell carcinoma (CSCC) and for the treatment of metastatic or locally advanced CSCC. These indications are already approved in the United States and European Union (EU).
• In October 2026, the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion recommending the approval of an alternative dosing schedule for Libtayo across all approved indications. The positive opinion supports reducing Libtayo dosing frequency from every three weeks to every six weeks after the first 12 weeks of treatment. The European Commission (EC) is expected to make a final decision in the coming months. There is also a supplemental Biologics License Application (sBLA) under review by the U.S. Food and Drug Administration (FDA), which has a target action date in March 2027.
• In October 2026, the Company announced longer-term data which showed increasing and clinically meaningful overall survival benefit for Libtayo as an adjuvant treatment for patients with CSCC. The results were presented at the European Society for Medical Oncology (ESMO) 2026 Meeting.
• The FDA accepted for review the resubmission of the BLA for Ordspono ™ (odronextamab) in relapsed or refractory diffuse large B-cell lymphoma (DLBCL), which has a target action date in February 2027.
• The Company announced that ubamatamab (MUC16 and CD3 bispecific antibody) showed a high rate of durable responses in an initial study in patients with advanced low-grade serous ovarian cancer (LGSOC). The data are from an ongoing Phase 1/2 trial and were presented at the International Gynecologic Cancer Society (IGCS) 2026 Annual Global Meeting. Based on these preliminary trial results, the Company has been enrolling a single-arm, potentially registrational LGSOC trial and is planning to initiate a confirmatory Phase 3 trial in this setting.
• In August 2026, the FDA approved Pasatru to reduce formation of new heterotopic ossification lesions and clinician-assessed flare-ups in adults with FOP. A regulatory application is also under review in the EU.
• The Company announced positive 84-week results from the Phase 3 trial for Pasatru in adults with FOP. These longer-term findings demonstrated sustained efficacy in halting new, rogue bone growth and in significantly reducing disease flare-ups, and were presented at the American Society for Bone and Mineral Research (ASBMR) Annual Meeting.
• A three-arm, placebo-controlled Phase 3 study was initiated to evaluate cenvacibart (an antibody to Factor XI (catalytic domain)), and amrecibart (an antibody to Factor XI (A2 domain)), individually, for the prevention of venous thromboembolism in patients with a peripherally inserted central catheter (PICC). 2 • The Company has an ongoing Phase 1/2 study for its RNAi therapy targeting CIDEB. Interim results from this randomized, placebo-controlled, first-in-human trial in adults with metabolic dysfunction-associated steatotic liver disease (MASLD) showed that a single dose was generally well tolerated and reduced liver fat by approximately 70% on average from baseline at 12 weeks, with effects sustained through 24 weeks of follow-up. The Company plans to present interim results at the American Association for the Study of Liver Diseases (AASLD) Meeting in November 2026 and to initiate a Phase 3 study in metabolic dysfunction-associated steatohepatitis (MASH)/MASLD in the fourth quarter of 2026.
• The Company plans to report results from the Phase 2 study for baloncibart (NPR1 antagonist antibody) in postural orthostatic tachycardia syndrome (POTS) at the American Autonomic Society (AAS) Meeting in November 2026. Additionally, the Company plans to initiate a Phase 3 study in POTS in the first half of 2027, pending regulatory feedback.
• The Company announced new results from the Phase 2 COURAGE trial evaluating trevogrumab (myostatin antibody) for its potential to prevent lean mass and muscle loss during GLP-1 receptor agonist-induced weight loss in people living with obesity. The results of the trial were presented at the European Association for the Study of Diabetes (EASD) Annual Meeting.
• A second Phase 3 study was initiated for REGN1908-1909, an investigational treatment for cat allergy.
• In October 2026, the Company and Sanofi amended their antibody collaboration, adding multiple next-generation, long-acting Regeneron-invented antibodies to the alliance. Under the terms of the agreement, the Company received an up-front payment of $1.0 billion, and is entitled to receive up to an additional $7.0 billion in the aggregate upon the achievement of certain development, regulatory, and sales-based milestones. The companies will equally share development and commercialization costs for the new programs, and, if commercialized, share any future profits equally on a global basis.
• In October 2026, the Company announced an agreement with the Biomedical Advanced Research and Development Authority (BARDA) to provide additional supply of Inmazeb ® for U.S. preparedness against Ebola disease. Under the terms of the agreement, the Company expects to deliver a pre-specified number of treatment doses of Inmazeb each year to the U.S. government beginning in 2027 through 2031. 3
EYLEA HD U.S. net product sales increased in the third quarter of 2026, compared to the third quarter of 2025, primarily due to higher sales volumes driven by increased demand, partly offset by a lower net selling price.
EYLEA U.S. net product sales decreased in the third quarter of 2026, compared to the third quarter of 2025, primarily due to lower sales volumes as a result of continued competitive pressures and the continued transition of patients to EYLEA HD. Libtayo U.S. net product sales increased in the third quarter of 2026, compared to the third quarter of 2025, primarily due to higher sales volumes driven by increased demand. Sanofi collaboration revenue increased in the third quarter of 2026, compared to the third quarter of 2025, due to an increase in the Company's share of profits from the commercialization of antibodies, which were $2.575 billion and $1.456 billion in the third quarter of 2026 and 2025, respectively. The increase in the Company's share of profits from the commercialization of antibodies was driven by higher profits primarily associated with an increase in Dupixent sales. In addition, the Sanofi Development Balance was fully repaid as of the end of the second quarter of 2026 and no longer reduced Sanofi collaboration revenue beginning in the third quarter of 2026.
GAAP and non-GAAP R&D expenses increased in the third quarter of 2026, compared to the third quarter of 2025, driven by the advancement of the Company's clinical pipeline and increased manufacturing activity associated with the Company's product candidates.
GAAP other income (expense), net decreased in the third quarter of 2026, compared to the third quarter of 2025, primarily due to lower net gains on marketable and other securities.
In the third quarter of 2026, the Company's GAAP effective tax rate (ETR) was 14.7%, compared to 17.2% in the third quarter of 2025. The GAAP ETR for the third quarter of 2025 was negatively impacted by the enactment of the "One Big Beautiful Bill Act" or "OBBBA," including a $45 million charge related to the re-measurement of the Company's U.S. net deferred tax assets. In the third quarter of 2026, the non-GAAP ETR was 15.0%, compared to 13.1% in the third quarter of 2025.
A reconciliation of the Company's GAAP to non-GAAP results is included in Table 3 of this press release.
During the nine months ended September 30, 2026, the Company repurchased $2.3 billion of its common stock. As of September 30, 2026, $2.2 billion remained available for share repurchases under the Company's share repurchase programs.
In October 2026, the Company declared a cash dividend of $0.94 per share on the Company's common stock and Class A stock, payable on December 3, 2026 to shareholders of record as of November 20, 2026. 5
The Company's full year 2026 financial guidance consists of the following components:
2026 Guidance Prior Updated GAAP R&D $6.500–$6.635 billion $6.600–$6.735 billion Non-GAAP R&D(a) $5.950–$6.050 billion $6.050–$6.150 billion GAAP SG&A $2.830–$2.960 billion $2.730–$2.860 billion Non-GAAP SG&A(a) $2.500–$2.600 billion $2.400–$2.500 billion GAAP gross margin on 78%–79% Approximately 80% net product sales Non-GAAP gross margin on net product 84%–85% Approximately 86% sales(a) GAAP COCM $985 million–$1.035 Unchanged billion Non-GAAP COCM(a) $970 million–$1.020 Unchanged billion Capital expenditures $1.030–$1.100 billion $1.050–$1.100 billion GAAP effective tax rate 13%–14% Approximately 14% Non-GAAP effective tax 14%–15% Approximately 15% rate(a) *The Company's 2026 financial guidance does not assume the completion of any business development transactions not completed as of the date of this press release
6 A reconciliation of full year 2026 GAAP to non-GAAP financial guidance is included below:
Projected Range ($ in millions) Low High ────────────────────────────────────────────────────────────────────────────── GAAP R&D $ 6,600 $ 6,735 Stock-based -550 -580 compensation expense Other — -5 Non-GAAP R&D(a) $ 6,050 $ 6,150 GAAP SG&A $ 2,730 $ 2,860 Stock-based -325 -350 compensation expense Other* -5 -10 Non-GAAP SG&A(a) $ 2,400 $ 2,500 GAAP gross margin on 80% 80% net product sales Stock-based 1% 1% compensation expense Other** 5% 5% Non-GAAP gross margin on net product 86% 86% sales(a) GAAP COCM $ 985 $ 1,035 Temporary manufacturing -15 -15 interruption-related costs Non-GAAP COCM(a) $ 970 $ 1,020 GAAP ETR 14% 14% Income tax effect of GAAP to non-GAAP 1% 1% reconciling items Income tax expense: Shortfall from -<1% -<1% stock-based compensation Non-GAAP ETR(a) 15% 15% *Includes litigation settlements and other costs **Includes intangible asset amortization and temporary manufacturing interruption-related costs
This press release uses non-GAAP R&D, non-GAAP SG&A, non-GAAP COGS, non-GAAP gross margin on net product sales, non-GAAP COCM, non-GAAP other income (expense), net, non-GAAP ETR, non-GAAP net income, non-GAAP net income per share, and free cash flow, which are financial measures that are not calculated in accordance with U.S. Generally Accepted Accounting Principles (GAAP). These non-GAAP financial measures are computed by excluding certain non-cash and/or other items from the related GAAP financial measure. The Company also includes a non-GAAP adjustment for the estimated income tax effect of reconciling items. A reconciliation of the Company's GAAP to non-GAAP results is included in Table 3 of this press release. The Company makes such adjustments for items the Company does not view as useful in evaluating its operating performance. For example, adjustments may be made for items that fluctuate from period to period based on factors that are not within the Company's control (such as the Company's stock price on the dates share-based grants are issued or changes in the fair value of the Company's investments (a) in equity securities) or items that are not associated with normal, recurring operations (such as acquisition and integration costs). Management uses these non-GAAP measures for planning, budgeting, forecasting, assessing historical performance, and making financial and operational decisions, and also provides forecasts to investors on this basis. With respect to free cash flow, the Company believes that this non-GAAP measure provides a further measure of the Company's ability to generate cash flows from its operations. Additionally, the non-GAAP measures presented are intended to provide investors with an enhanced understanding of the financial performance of the Company's core business operations. However, there are limitations in the use of these and other non-GAAP financial measures as they exclude certain expenses that are recurring in nature. Furthermore, the Company's non-GAAP financial measures may not be comparable with non-GAAP information provided by other companies. Any non-GAAP financial measure presented by the Company should be considered supplemental to, and not a substitute for, measures of financial performance prepared in accordance with GAAP. Gross margin on net product sales represents gross profit expressed (b) as a percentage of total net product sales recorded by the Company. Gross profit is calculated as net product sales less cost of goods sold. (c) Corresponding reimbursements from collaborators and others for manufacturing product is recorded within revenues.
Regeneron will host a conference call and simultaneous webcast to discuss its third quarter 2026 financial and operating results on Friday, October 30, 2026, at 8:30 AM Eastern Time. Participants may access the conference call live via webcast, or register in advance and participate via telephone, on the "Investors and Media" page of Regeneron's website at www.regeneron.com. Upon registration, all telephone participants will receive a confirmation email detailing how to join the conference call, including the dial-in number along with a unique passcode and registrant ID that can be used to access the call. A replay and transcript of the conference call and webcast will be archived on the Company's website for at least 30 days.
Regeneron is a leading biotechnology company that invents, develops, and commercializes life-transforming medicines for people with serious diseases. Founded and led by physician-scientists, Regeneron's unique ability to repeatedly and consistently translate science into medicine has led to numerous approved treatments and product candidates in development, most of which were homegrown in Regeneron's laboratories. Regeneron's medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurological diseases, hematologic conditions, infectious diseases, and rare diseases.
Regeneron pushes the boundaries of scientific discovery and accelerates drug development using its proprietary technologies, such as VelociSuite ® , which produces optimized fully human antibodies and new classes of bispecific antibodies. Regeneron is shaping the next frontier of medicine with data-powered insights from the Regeneron Genetics Center ® and pioneering genetic medicine platforms, enabling Regeneron to identify innovative targets and complementary approaches to potentially treat or cure diseases.
For more information, please visit www.regeneron.com or follow Regeneron on LinkedIn, Instagram, Facebook, or X.
This press release includes forward-looking statements that involve risks and uncertainties relating to future events and the future performance of Regeneron Pharmaceuticals, Inc. ("Regeneron" or the "Company"), and actual events or results may differ materially from these forward-looking statements. Words such as "anticipate," "expect," "intend," "plan," "believe," "seek," "estimate," variations of such words, and similar expressions are intended to identify such forward-looking statements, although not all forward-looking statements contain these identifying words. These statements concern, and these risks and uncertainties include, among others, competing products and product candidates (including biosimilar products) that may be superior to, or more cost effective than, products marketed or otherwise commercialized by Regeneron and/or its collaborators or licensees (collectively, "Regeneron's Products") and product candidates being developed by Regeneron and/or its collaborators or licensees (collectively, "Regeneron's Product Candidates"); uncertainty of the utilization, market acceptance, and commercial success of Regeneron's Products and Regeneron's Product Candidates and the impact of studies (whether conducted by Regeneron or others and whether mandated or voluntary) or recommendations and guidelines from governmental authorities and other third parties or other factors beyond Regeneron's control on the commercial success of Regeneron's Products and Regeneron's Product Candidates; the nature, timing, and possible success and therapeutic applications of Regeneron's Products and Regeneron's Product 9 Candidates and research and clinical programs now underway or planned, including without limitation EYLEA HD ® (aflibercept) Injection 8 mg, EYLEA
(lunsotogene parvec), Pasatru ™ (garetosmab), other clinical programs discussed in this press release, Regeneron's and its collaborators' earlier-stage programs, and the use of human genetics in Regeneron's research programs; the likelihood and timing of achieving any of the anticipated milestones described in this press release; safety issues resulting from the administration of Regeneron's Products and Regeneron's Product Candidates in patients, including serious complications or side effects in connection with the use of Regeneron’s Products and Regeneron's Product Candidates in clinical trials; the likelihood, timing, and scope of possible regulatory approval and commercial launch of Regeneron's Product Candidates and new indications for Regeneron's Products, including those listed above and/or otherwise discussed in this press release; the extent to which the results from the research and development programs conducted by Regeneron and/or its collaborators may be replicated in other studies and/or lead to advancement of product candidates to clinical trials, therapeutic applications, or regulatory approval; ongoing regulatory obligations and oversight impacting Regeneron's Products, research and clinical programs, and business, including those relating to patient privacy; determinations by regulatory and administrative governmental authorities which may delay or restrict Regeneron's ability to continue to develop or commercialize Regeneron's Products and Regeneron's Product Candidates; the ability of Regeneron to manufacture and manage supply chains for multiple products and product candidates and risks associated with tariffs and other trade restrictions; the ability of Regeneron’s collaborators, suppliers, or other third parties (as applicable) to perform manufacturing, filling, finishing, packaging, labeling, distribution, and other steps related to Regeneron’s Products and Regeneron's Product Candidates; the availability and extent of reimbursement or copay assistance for Regeneron’s Products from third-party payors and other third parties, including private payor healthcare and insurance programs, health maintenance organizations, pharmacy benefit management companies, and government programs such as Medicare and Medicaid; coverage and reimbursement determinations by such payors and other third parties and new policies and procedures adopted by such payors and other third parties; changes to drug pricing regulations and requirements and Regeneron's drug pricing strategy, including in connection with Regeneron's April 2026 agreements with the U.S. government; other changes in laws, regulations, and policies affecting the healthcare industry; unanticipated expenses; the costs of developing, producing, and selling products; the ability of Regeneron to meet any of its financial projections or guidance and changes to the assumptions underlying those projections or guidance, including GAAP and non-GAAP R&D, GAAP and non-GAAP SG&A, GAAP and non-GAAP gross margin on net product sales, GAAP and non-GAAP COCM, capital expenditures, and GAAP and non-GAAP ETR; the potential for any license or collaboration agreement, including Regeneron's agreements with Sanofi and Bayer (or their respective affiliated companies, as applicable), to be cancelled or terminated; the impact of public health outbreaks, epidemics, or pandemics on Regeneron's business; and risks associated with litigation and other proceedings and government investigations relating to the Company and/or its operations (including the pending civil proceedings initiated or joined by the U.S. Department of Justice and the U.S. Attorney's Office for the District of Massachusetts), risks associated with intellectual property of the Company or other parties and pending or future litigation or patent office proceedings relating thereto (including without limitation patent litigation and other related proceedings relating to Regeneron's Products), the ultimate outcome of any such proceedings and investigations, and the impact any of the foregoing may have on Regeneron’s business, 10 prospects, operating results, and financial condition. A more complete description of these and other material risks can be found in Regeneron's filings with the U.S. Securities and Exchange Commission, including its Form 10-K for the fiscal year ended December 31, 2025 and its Form 10-Q for the quarterly period ended September 30, 2026. Any forward-looking statements are made based on management's current beliefs and judgment, and the reader is cautioned not to rely on any forward-looking statements made by Regeneron. Regeneron does not undertake any obligation to update (publicly or otherwise) any forward-looking statement, including without limitation any financial projection or guidance, whether as a result of new information, future events, or otherwise.
Regeneron uses its media and investor relations website and social media outlets to publish important information about the Company, including information that may be deemed material to investors. Financial and other information about Regeneron is routinely posted and is accessible on Regeneron's media and investor relations website (https://investor.regeneron.com) and its LinkedIn page (https://www.linkedin.com/company/regeneron-pharmaceuticals).
This press release and/or the financial results attached to this press release include amounts that are considered "non-GAAP financial measures" under SEC rules. As required, Regeneron has provided reconciliations of such non-GAAP financial measures. ###
Contact Information: Ryan Crowe Christina Chan Investor Relations Corporate Affairs 914-847-8790 914-847-8827 ryan.crowe@regeneron.com christina.chan@regeneron.com
RECONCILIATION OF GAAP TO NON-GAAP FINANCIAL INFORMATION (Unaudited) (continued)
Full text with the tables
Exhibit 99.1
Press Release
Regeneron Reports Third Quarter 2026 Financial and Operating Results
• Third quarter 2026 revenues increased 36% to $5.1 billion versus third quarter
2025
• Dupixent ® global net sales (recorded by Sanofi) increased 35% to $6.5 billion
• EYLEA HD ® U.S. net sales increased 62% to $699 million
• Libtayo ® global net sales increased 51% to $550 million
• GAAP EPS increased 35% to $18.45; non-GAAP EPS (a) increased 70% to $20.07
• Expanded collaboration with Sanofi, adding multiple next-generation, long-
acting immunology antibodies; $1.0 billion up-front to be recognized as
collaboration revenue in fourth quarter 2026 with potential to receive up to an
additional $7.0 billion in future milestones
• Pasatru ™ (garetosmab) approved by FDA for fibrodysplasia ossificans
progressiva (FOP)
Tarrytown, New York (October 30, 2026) --
Regeneron Pharmaceuticals, Inc. (Nasdaq:
REGN
) today announced financial results for the third quarter of 2026 and provided a
business update.
"This was an outstanding quarter for Regeneron, with Dupixent, EYLEA HD, and
Libtayo each achieving record net sales," said Leonard S. Schleifer, M.D.,
Ph.D., Board co-Chair, President and Chief Executive Officer of Regeneron. "Our
pipeline of about 50 product candidates is rapidly advancing. We expect an FDA
decision for cemdisiran in generalized myasthenia gravis next month; our Phase 3
programs in multiple myeloma, lymphoma, anticoagulation, and obesity continue to
advance; and we have generated encouraging early data in MASH, POTS, and ovarian
cancer. Finally, we expanded our alliance with Sanofi to include four Regeneron-
invented, next-generation, long-acting antibodies designed to build on the
success of Dupixent."
Financial Highlights
($ in millions,
except per
share data) Q3 2026 Q3 2025 % Change
──────────────────────────────────────────────────────────────────────────────
Total revenues $ 5,116 $ 3,754 36 %
GAAP net income $ 1,949 $ 1,460 33 %
GAAP net income
per share - $ 18.45 $ 13.62 35 %
diluted
Non-GAAP net $ 2,150 $ 1,287 67 %
income(a)
Non-GAAP net
income per $ 20.07 $ 11.83 70 %
share -
diluted(a)
"We are pleased with our third quarter financial results, which marked our third
consecutive quarter of double-digit growth in both revenue and non-GAAP EPS,"
said Christopher Fenimore, Executive Vice President, Finance and Chief Financial
Officer of Regeneron. "Strong commercial execution across our portfolio,
together with the anticipated step-up in Sanofi collaboration revenue in the
first full quarter following repayment of the Development Balance, drove a 36%
increase in total revenues and a 70% increase in non-GAAP EPS, positioning us to
deliver one of our strongest years ever."
1
Business Highlights
Key Pipeline Progress
Regeneron has approximately 50 product candidates in clinical development,
including a number of marketed products for which it is investigating additional
indications. Updates from the clinical pipeline include:
Libtayo (cemiplimab)
• In August 2026, the Ministry of Health, Labour and Welfare (MHLW) in Japan
approved Libtayo as an adjuvant treatment for cutaneous squamous cell carcinoma
(CSCC) and for the treatment of metastatic or locally advanced CSCC. These
indications are already approved in the United States and European Union (EU).
• In October 2026, the European Medicines Agency’s (EMA) Committee for Medicinal
Products for Human Use (CHMP) adopted a positive opinion recommending the
approval of an alternative dosing schedule for Libtayo across all approved
indications. The positive opinion supports reducing Libtayo dosing frequency
from every three weeks to every six weeks after the first 12 weeks of treatment.
The European Commission (EC) is expected to make a final decision in the coming
months. There is also a supplemental Biologics License Application (sBLA) under
review by the U.S. Food and Drug Administration (FDA), which has a target action
date in March 2027.
• In October 2026, the Company announced longer-term data which showed
increasing and clinically meaningful overall survival benefit for Libtayo as an
adjuvant treatment for patients with CSCC. The results were presented at the
European Society for Medical Oncology (ESMO) 2026 Meeting.
Other Oncology Programs
• The FDA accepted for review the resubmission of the BLA for Ordspono ™
(odronextamab) in relapsed or refractory diffuse large B-cell lymphoma (DLBCL),
which has a target action date in February 2027.
• The Company announced that ubamatamab (MUC16 and CD3 bispecific antibody)
showed a high rate of durable responses in an initial study in patients with
advanced low-grade serous ovarian cancer (LGSOC). The data are from an ongoing
Phase 1/2 trial and were presented at the International Gynecologic Cancer
Society (IGCS) 2026 Annual Global Meeting. Based on these preliminary trial
results, the Company has been enrolling a single-arm, potentially registrational
LGSOC trial and is planning to initiate a confirmatory Phase 3 trial in this
setting.
Pasatru (garetosmab)
• In August 2026, the FDA approved Pasatru to reduce formation of new
heterotopic ossification lesions and clinician-assessed flare-ups in adults with
FOP. A regulatory application is also under review in the EU.
• The Company announced positive 84-week results from the Phase 3 trial for
Pasatru in adults with FOP. These longer-term findings demonstrated sustained
efficacy in halting new, rogue bone growth and in significantly reducing disease
flare-ups, and were presented at the American Society for Bone and Mineral
Research (ASBMR) Annual Meeting.
Other Programs
• A three-arm, placebo-controlled Phase 3 study was initiated to evaluate
cenvacibart (an antibody to Factor XI (catalytic domain)), and amrecibart (an
antibody to Factor XI (A2 domain)), individually, for the prevention of venous
thromboembolism in patients with a peripherally inserted central catheter
(PICC).
2
• The Company has an ongoing Phase 1/2 study for its RNAi therapy targeting
CIDEB. Interim results from this randomized, placebo-controlled, first-in-human
trial in adults with metabolic dysfunction-associated steatotic liver disease
(MASLD) showed that a single dose was generally well tolerated and reduced liver
fat by approximately 70% on average from baseline at 12 weeks, with effects
sustained through 24 weeks of follow-up. The Company plans to present interim
results at the American Association for the Study of Liver Diseases (AASLD)
Meeting in November 2026 and to initiate a Phase 3 study in metabolic
dysfunction-associated steatohepatitis (MASH)/MASLD in the fourth quarter of
2026.
• The Company plans to report results from the Phase 2 study for baloncibart
(NPR1 antagonist antibody) in postural orthostatic tachycardia syndrome (POTS)
at the American Autonomic Society (AAS) Meeting in November 2026. Additionally,
the Company plans to initiate a Phase 3 study in POTS in the first half of 2027,
pending regulatory feedback.
• The Company announced new results from the Phase 2 COURAGE trial evaluating
trevogrumab (myostatin antibody) for its potential to prevent lean mass and
muscle loss during GLP-1 receptor agonist-induced weight loss in people living
with obesity. The results of the trial were presented at the European
Association for the Study of Diabetes (EASD) Annual Meeting.
• A second Phase 3 study was initiated for REGN1908-1909, an investigational
treatment for cat allergy.
Corporate Updates
• In October 2026, the Company and Sanofi amended their antibody collaboration,
adding multiple next-generation, long-acting Regeneron-invented antibodies to
the alliance. Under the terms of the agreement, the Company received an up-front
payment of $1.0 billion, and is entitled to receive up to an additional $7.0
billion in the aggregate upon the achievement of certain development,
regulatory, and sales-based milestones. The companies will equally share
development and commercialization costs for the new programs, and, if
commercialized, share any future profits equally on a global basis.
• In October 2026, the Company announced an agreement with the Biomedical
Advanced Research and Development Authority (BARDA) to provide additional supply
of Inmazeb ® for U.S. preparedness against Ebola disease. Under the terms of the
agreement, the Company expects to deliver a pre-specified number of treatment
doses of Inmazeb each year to the U.S. government beginning in 2027 through
2031.
3
Third Quarter 2026 Financial Results
Revenues
($ in millions)
Net product sales: Q3 2026 Q3 2025 % Change
──────────────────────────────────────────────────────────────────────────────
EYLEA HD - U.S. $ 699 $ 431 62 %
EYLEA®- U.S. 400 681 (41 %)
Total EYLEA HD and 1,099 1,112 (1 %)
EYLEA - U.S.
Libtayo - U.S. 396 219 81 %
Libtayo - ROW* 154 146 5 %
Total Libtayo - 550 365 51 %
Global
Praluent®-U.S. 81 67 21 %
Evkeeza®- U.S. 55 43 28 %
Lynozyfic®- Global 19 1 **
Other products - 1 — **
Global
Total net product 1,805 1,588 14 %
sales
Collaboration
revenue:
Sanofi 2,724 1,617 68 %
Bayer 267 345 (23 %)
Other 10 6 67 %
Other revenue 310 198 57 %
Total revenues $ 5,116 $ 3,754 36 %
*Rest of world
(ROW)
**Percentage not
meaningful or
greater
than 100%
EYLEA HD U.S. net product sales increased in the third quarter of 2026, compared
to the third quarter of 2025, primarily due to higher sales volumes driven by
increased demand, partly offset by a lower net selling price.
EYLEA U.S. net product sales decreased in the third quarter of 2026, compared to
the third quarter of 2025, primarily due to lower sales volumes as a result of
continued competitive pressures and the continued transition of patients to
EYLEA HD.
Libtayo U.S. net product sales increased in the third quarter of 2026, compared
to the third quarter of 2025, primarily due to higher sales volumes driven by
increased demand.
Sanofi collaboration revenue increased in the third quarter of 2026, compared to
the third quarter of 2025, due to an increase in the Company's share of profits
from the commercialization of antibodies, which were $2.575 billion and $1.456
billion in the third quarter of 2026 and 2025, respectively. The increase in the
Company's share of profits from the commercialization of antibodies was driven
by higher profits primarily associated with an increase in Dupixent sales. In
addition, the Sanofi Development Balance was fully repaid as of the end of the
second quarter of 2026 and no longer reduced Sanofi collaboration revenue
beginning in the third quarter of 2026.
Refer to Table 4 for a summary of collaboration revenue.
4
Operating Expenses
…
… … % … … %
… … … … N… … C…
──────────────────────────────────────────────────────────────────────────────
$ … $ … … % $ … $ 1… … %
$ … $ … … … * * *
$ … $ … 3 % $ … $ 5… 9 %
$ … $ … … % $ … $ 2… 8 %
… … 8… …
$ … $ … 5 % * * *
$ — $ … … … * * *
GAAP and non-GAAP R&D expenses increased in the third quarter of 2026, compared
to the third quarter of 2025, driven by the advancement of the Company's
clinical pipeline and increased manufacturing activity associated with the
Company's product candidates.
Other Financial Information
GAAP other income (expense), net decreased in the third quarter of 2026,
compared to the third quarter of 2025, primarily due to lower net gains on
marketable and other securities.
In the third quarter of 2026, the Company's GAAP effective tax rate (ETR) was
14.7%, compared to 17.2% in the third quarter of 2025. The GAAP ETR for the
third quarter of 2025 was negatively impacted by the enactment of the "One Big
Beautiful Bill Act" or "OBBBA," including a $45 million charge related to the
re-measurement of the Company's U.S. net deferred tax assets. In the third
quarter of 2026, the non-GAAP ETR was 15.0%, compared to 13.1% in the third
quarter of 2025.
A reconciliation of the Company's GAAP to non-GAAP results is included in Table
3 of this press release.
Capital Allocation
During the nine months ended September 30, 2026, the Company repurchased $2.3
billion of its common stock. As of September 30, 2026, $2.2 billion remained
available for share repurchases under the Company's share repurchase programs.
In October 2026, the Company declared a cash dividend of $0.94 per share on the
Company's common stock and Class A stock, payable on December 3, 2026 to
shareholders of record as of November 20, 2026.
5
2026 Financial Guidance*
The Company's full year 2026 financial guidance consists of the following
components:
2026 Guidance
Prior Updated
GAAP R&D $6.500–$6.635 billion $6.600–$6.735 billion
Non-GAAP R&D(a) $5.950–$6.050 billion $6.050–$6.150 billion
GAAP SG&A $2.830–$2.960 billion $2.730–$2.860 billion
Non-GAAP SG&A(a) $2.500–$2.600 billion $2.400–$2.500 billion
GAAP gross margin on 78%–79% Approximately 80%
net product sales
Non-GAAP gross margin
on net product 84%–85% Approximately 86%
sales(a)
GAAP COCM $985 million–$1.035 Unchanged
billion
Non-GAAP COCM(a) $970 million–$1.020 Unchanged
billion
Capital expenditures $1.030–$1.100 billion $1.050–$1.100 billion
GAAP effective tax rate 13%–14% Approximately 14%
Non-GAAP effective tax 14%–15% Approximately 15%
rate(a)
*The Company's 2026
financial guidance
does not assume the
completion of any
business development
transactions not
completed as of the
date of this press
release
6
A reconciliation of full year 2026 GAAP to non-GAAP financial guidance is
included below:
Projected Range
($ in millions) Low High
──────────────────────────────────────────────────────────────────────────────
GAAP R&D $ 6,600 $ 6,735
Stock-based -550 -580
compensation expense
Other — -5
Non-GAAP R&D(a) $ 6,050 $ 6,150
GAAP SG&A $ 2,730 $ 2,860
Stock-based -325 -350
compensation expense
Other* -5 -10
Non-GAAP SG&A(a) $ 2,400 $ 2,500
GAAP gross margin on 80% 80%
net product sales
Stock-based 1% 1%
compensation expense
Other** 5% 5%
Non-GAAP gross margin
on net product 86% 86%
sales(a)
GAAP COCM $ 985 $ 1,035
Temporary
manufacturing -15 -15
interruption-related
costs
Non-GAAP COCM(a) $ 970 $ 1,020
GAAP ETR 14% 14%
Income tax effect of
GAAP to non-GAAP 1% 1%
reconciling items
Income tax expense:
Shortfall from -<1% -<1%
stock-based
compensation
Non-GAAP ETR(a) 15% 15%
*Includes litigation
settlements and
other costs
**Includes intangible
asset amortization
and temporary
manufacturing
interruption-related
costs
7
This press release uses non-GAAP R&D, non-GAAP SG&A, non-GAAP COGS,
non-GAAP gross margin on net product sales, non-GAAP COCM, non-GAAP
other income (expense), net, non-GAAP ETR, non-GAAP net income,
non-GAAP net income per share, and free cash flow, which are
financial measures that are not calculated in accordance with U.S.
Generally Accepted Accounting Principles (GAAP). These non-GAAP
financial measures are computed by excluding certain non-cash and/or
other items from the related GAAP financial measure. The Company also
includes a non-GAAP adjustment for the estimated income tax effect of
reconciling items. A reconciliation of the Company's GAAP to non-GAAP
results is included in Table 3 of this press release.
The Company makes such adjustments for items the Company does not
view as useful in evaluating its operating performance. For example,
adjustments may be made for items that fluctuate from period to
period based on factors that are not within the Company's control
(such as the Company's stock price on the dates share-based grants
are issued or changes in the fair value of the Company's investments
(a) in equity securities) or items that are not associated with normal,
recurring operations (such as acquisition and integration costs).
Management uses these non-GAAP measures for planning, budgeting,
forecasting, assessing historical performance, and making financial
and operational decisions, and also provides forecasts to investors
on this basis. With respect to free cash flow, the Company believes
that this non-GAAP measure provides a further measure of the
Company's ability to generate cash flows from its operations.
Additionally, the non-GAAP measures presented are intended to provide
investors with an enhanced understanding of the financial performance
of the Company's core business operations. However, there are
limitations in the use of these and other non-GAAP financial measures
as they exclude certain expenses that are recurring in nature.
Furthermore, the Company's non-GAAP financial measures may not be
comparable with non-GAAP information provided by other companies. Any
non-GAAP financial measure presented by the Company should be
considered supplemental to, and not a substitute for, measures of
financial performance prepared in accordance with GAAP.
Gross margin on net product sales represents gross profit expressed
(b) as a percentage of total net product sales recorded by the Company.
Gross profit is calculated as net product sales less cost of goods
sold.
(c) Corresponding reimbursements from collaborators and others for
manufacturing product is recorded within revenues.
8
Conference Call Information
Regeneron will host a conference call and simultaneous webcast to discuss its
third quarter 2026 financial and operating results on Friday, October 30, 2026,
at 8:30 AM Eastern Time. Participants may access the conference call live via
webcast, or register in advance and participate via telephone, on the "Investors
and Media" page of Regeneron's website at www.regeneron.com. Upon registration,
all telephone participants will receive a confirmation email detailing how to
join the conference call, including the dial-in number along with a unique
passcode and registrant ID that can be used to access the call. A replay and
transcript of the conference call and webcast will be archived on the Company's
website for at least 30 days.
About Regeneron
Regeneron is a leading biotechnology company that invents, develops, and
commercializes life-transforming medicines for people with serious diseases.
Founded and led by physician-scientists, Regeneron's unique ability to
repeatedly and consistently translate science into medicine has led to numerous
approved treatments and product candidates in development, most of which were
homegrown in Regeneron's laboratories. Regeneron's medicines and pipeline are
designed to help patients with eye diseases, allergic and inflammatory diseases,
cancer, cardiovascular and metabolic diseases, neurological diseases,
hematologic conditions, infectious diseases, and rare diseases.
Regeneron pushes the boundaries of scientific discovery and accelerates drug
development using its proprietary technologies, such as VelociSuite ® , which
produces optimized fully human antibodies and new classes of bispecific
antibodies. Regeneron is shaping the next frontier of medicine with data-powered
insights from the Regeneron Genetics Center ® and pioneering genetic medicine
platforms, enabling Regeneron to identify innovative targets and complementary
approaches to potentially treat or cure diseases.
For more information, please visit www.regeneron.com or follow Regeneron on
LinkedIn, Instagram, Facebook, or X.
Forward-Looking Statements and Use of Digital Media
This press release includes forward-looking statements that involve risks and
uncertainties relating to future events and the future performance of Regeneron
Pharmaceuticals, Inc. ("Regeneron" or the "Company"), and actual events or
results may differ materially from these forward-looking statements. Words such
as "anticipate," "expect," "intend," "plan," "believe," "seek," "estimate,"
variations of such words, and similar expressions are intended to identify such
forward-looking statements, although not all forward-looking statements contain
these identifying words. These statements concern, and these risks and
uncertainties include, among others, competing products and product candidates
(including biosimilar products) that may be superior to, or more cost effective
than, products marketed or otherwise commercialized by Regeneron and/or its
collaborators or licensees (collectively, "Regeneron's Products") and product
candidates being developed by Regeneron and/or its collaborators or licensees
(collectively, "Regeneron's Product Candidates"); uncertainty of the
utilization, market acceptance, and commercial success of Regeneron's Products
and Regeneron's Product Candidates and the impact of studies (whether conducted
by Regeneron or others and whether mandated or voluntary) or recommendations and
guidelines from governmental authorities and other third parties or other
factors beyond Regeneron's control on the commercial success of Regeneron's
Products and Regeneron's Product Candidates; the nature, timing, and possible
success and therapeutic applications of Regeneron's Products and Regeneron's
Product
9
Candidates and research and clinical programs now underway or planned, including
without limitation EYLEA HD ® (aflibercept) Injection 8 mg, EYLEA
®
(aflibercept) Injection, Dupixent
®
(dupilumab), Libtayo
®
(cemiplimab), Praluent
®
(alirocumab), Kevzara
®
(sarilumab), Evkeeza
®
(evinacumab), Veopoz
®
(pozelimab), Ordspono ™ (odronextamab), Lynozyfic
®
(linvoseltamab), Otarmeni
®
(lunsotogene parvec), Pasatru ™ (garetosmab), other clinical programs discussed
in this press release, Regeneron's and its collaborators' earlier-stage
programs, and the use of human genetics in Regeneron's research programs; the
likelihood and timing of achieving any of the anticipated milestones described
in this press release; safety issues resulting from the administration of
Regeneron's Products and Regeneron's Product Candidates in patients, including
serious complications or side effects in connection with the use of Regeneron’s
Products and Regeneron's Product Candidates in clinical trials; the likelihood,
timing, and scope of possible regulatory approval and commercial launch of
Regeneron's Product Candidates and new indications for Regeneron's Products,
including those listed above and/or otherwise discussed in this press release;
the extent to which the results from the research and development programs
conducted by Regeneron and/or its collaborators may be replicated in other
studies and/or lead to advancement of product candidates to clinical trials,
therapeutic applications, or regulatory approval; ongoing regulatory obligations
and oversight impacting Regeneron's Products, research and clinical programs,
and business, including those relating to patient privacy; determinations by
regulatory and administrative governmental authorities which may delay or
restrict Regeneron's ability to continue to develop or commercialize Regeneron's
Products and Regeneron's Product Candidates; the ability of Regeneron to
manufacture and manage supply chains for multiple products and product
candidates and risks associated with tariffs and other trade restrictions; the
ability of Regeneron’s collaborators, suppliers, or other third parties (as
applicable) to perform manufacturing, filling, finishing, packaging, labeling,
distribution, and other steps related to Regeneron’s Products and Regeneron's
Product Candidates; the availability and extent of reimbursement or copay
assistance for Regeneron’s Products from third-party payors and other third
parties, including private payor healthcare and insurance programs, health
maintenance organizations, pharmacy benefit management companies, and government
programs such as Medicare and Medicaid; coverage and reimbursement
determinations by such payors and other third parties and new policies and
procedures adopted by such payors and other third parties; changes to drug
pricing regulations and requirements and Regeneron's drug pricing strategy,
including in connection with Regeneron's April 2026 agreements with the U.S.
government; other changes in laws, regulations, and policies affecting the
healthcare industry; unanticipated expenses; the costs of developing, producing,
and selling products; the ability of Regeneron to meet any of its financial
projections or guidance and changes to the assumptions underlying those
projections or guidance, including GAAP and non-GAAP R&D, GAAP and non-GAAP
SG&A, GAAP and non-GAAP gross margin on net product sales, GAAP and non-GAAP
COCM, capital expenditures, and GAAP and non-GAAP ETR; the potential for any
license or collaboration agreement, including Regeneron's agreements with Sanofi
and Bayer (or their respective affiliated companies, as applicable), to be
cancelled or terminated; the impact of public health outbreaks, epidemics, or
pandemics on Regeneron's business; and risks associated with litigation and
other proceedings and government investigations relating to the Company and/or
its operations (including the pending civil proceedings initiated or joined by
the U.S. Department of Justice and the U.S. Attorney's Office for the District
of Massachusetts), risks associated with intellectual property of the Company or
other parties and pending or future litigation or patent office proceedings
relating thereto (including without limitation patent litigation and other
related proceedings relating to Regeneron's Products), the ultimate outcome of
any such proceedings and investigations, and the impact any of the foregoing may
have on Regeneron’s business,
10
prospects, operating results, and financial condition. A more complete
description of these and other material risks can be found in Regeneron's
filings with the U.S. Securities and Exchange Commission, including its Form
10-K for the fiscal year ended December 31, 2025 and its Form 10-Q for the
quarterly period ended September 30, 2026. Any forward-looking statements are
made based on management's current beliefs and judgment, and the reader is
cautioned not to rely on any forward-looking statements made by Regeneron.
Regeneron does not undertake any obligation to update (publicly or otherwise)
any forward-looking statement, including without limitation any financial
projection or guidance, whether as a result of new information, future events,
or otherwise.
Regeneron uses its media and investor relations website and social media outlets
to publish important information about the Company, including information that
may be deemed material to investors. Financial and other information about
Regeneron is routinely posted and is accessible on Regeneron's media and
investor relations website (https://investor.regeneron.com) and its LinkedIn
page (https://www.linkedin.com/company/regeneron-pharmaceuticals).
Non-GAAP Financial Measures
This press release and/or the financial results attached to this press release
include amounts that are considered "non-GAAP financial measures" under SEC
rules. As required, Regeneron has provided reconciliations of such non-GAAP
financial measures.
###
Contact Information:
Ryan Crowe Christina Chan
Investor Relations Corporate Affairs
914-847-8790 914-847-8827
ryan.crowe@regeneron.com christina.chan@regeneron.com
11
TABLE 1
REGENERON PHARMACEUTICALS, INC.
CONDENSED CONSOLIDATED BALANCE SHEETS (Unaudited)
(In millions)
September 30, December 31,
Assets: 2026 2025
──────────────────────────────────────────────────────────────────────────────
Cash and marketable $ 18,858.5 $ 18,865.8
securities
Accounts receivable, 7,578.6 5,741.1
net
Inventories 2,894.6 3,200.8
Property, plant, and 5,727.5 5,120.4
equipment, net
Intangible assets, net 1,315.5 1,257.4
Deferred tax assets 4,535.6 4,077.2
Other assets 3,494.9 2,296.0
Total assets $ 44,405.2 $ 40,558.7
Liabilities and
stockholders' equity:
Accounts payable,
accrued expenses, and $ 7,229.7 $ 5,834.2
other liabilities
Finance lease 720.0 720.0
liabilities
Deferred revenue 970.0 761.7
Long-term debt 1,987.0 1,985.9
Stockholders' equity 33,498.5 31,256.9
Total liabilities and
stockholders' $ 44,405.2 $ 40,558.7
equity
12
TABLE 2
REGENERON PHARMACEUTICALS, INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS (Unaudited)
(In millions, except per share data)
Three Nine
Months Months
Ended Ended
Septem… Septe…
30, 30,
Reve… 2026 2025 2026 2025
──────────────────────────────────────────────────────────────────────────────
Net
prod… $ 1,805… $ 1,587.7 $ 4,982.2 $ 4,634…
sales
Coll… 3,000… 1,968.4 7,355.2 5,360…
reve…
Other 310.0 198.2 674.5 464.0
reve…
5,115… 3,754.3 13,011… 10,45…
Expe…
Rese…
and 1,794… 1,475.0 4,969.8 4,224…
deve…
Acqu…
in-p…
rese… 21.5 83.1 250.4 105.4
and
deve…
Sell…
gene… 677.8 657.8 1,987.6 1,925…
and
admi…
Cost
of 321.7 281.0 1,055.8 822.1
goods
sold
Cost
of
coll… 251.9 240.6 763.7 694.0
and
cont…
manu…
Other
oper…
(inc… — -10.0 — -10.0
expe…
net
3,067… 2,727.5 9,027.3 7,760…
Inco…
from 2,048… 1,026.8 3,984.6 2,698…
oper…
Other
inco…
(exp…
Other
inco… 246.5 755.8 693.0 1,520…
(exp…
net
Inte… -10.6 -19.3 -34.5 -31.6
expe…
235.9 736.5 658.5 1,489…
Inco…
befo… 2,284… 1,763.3 4,643.1 4,187…
inco…
taxes
Inco…
tax 335.4 303.3 670.3 526.7
expe…
Net $ 1,948… $ 1,460.0 $ 3,972.8 $ 3,660…
inco…
Net
inco…
per $ 19.16 $ 14.09 $ 38.65 $ 34.83
share
-
basic
Net
inco…
per $ 18.45 $ 13.62 $ 37.37 $ 33.61
share
-
dilu…
Weig…
aver…
shar… 101.7 103.6 102.8 105.1
outs…
-
basic
Weig…
aver…
shar… 105.6 107.2 106.3 108.9
outs…
-
dilu…
13
TABLE 3
REGENERON PHARMACEUTICALS, INC.
RECONCILIATION OF GAAP TO NON-GAAP FINANCIAL INFORMATION (Unaudited)
(In millions, except per share data)
Three Nine
Months Months
Ended Ended
Septem… Septemb…
2026 30, 2025 2026 30, 2025
──────────────────────────────────────────────────────────────────────────────
GAAP $ 1,794.7 $ 1,475.0 $ 4,969.8 $ 4,224.1
R&D
Stock-…
compen… -140.3 -125.1 -406.2 -405.1
expense
Other -0.6 — -1.2 —
costs
Non-GA… $ 1,653.8 $ 1,349.9 $ 4,562.4 $ 3,819.0
R&D
GAAP $ 677.8 $ 657.8 $ 1,987.6 $ 1,925.0
SG&A
Stock-…
compen… -86.6 -92.0 -261.3 -279.0
expense
Litiga… — -25.0 5.0 -25.0
settle…
Other -2.9 — -8.8 -0.8
costs
Non-GA… $ 588.3 $ 540.8 $ 1,722.5 $ 1,620.2
SG&A
GAAP $ 321.7 $ 281.0 $ 1,055.8 $ 822.1
COGS
Stock-…
compen… -28.9 -19.9 -88.7 -60.3
expense
Intang…
asset -47.1 -33.7 -130.3 -94.8
amorti…
expense
Tempor…
manufa… — — -161.3 —
interr…
costs
Non-GA… $ 245.7 $ 227.4 $ 675.5 $ 667.0
COGS
GAAP $ 251.9 $ 240.6 $ 763.7 $ 694.0
COCM
Tempor…
manufa… — — -14.8 —
interr…
costs
Non-GA… $ 251.9 $ 240.6 $ 748.9 $ 694.0
COCM
GAAP
other
income $ 235.9 $ 736.5 $ 658.5 $ 1,489.0
(expen…
net
Gains
on
market…
and -60.3 -577.7 -147.2 -967.6
other
securi…
net
Non-GA…
other
income $ 175.6 $ 158.8 $ 511.3 $ 521.4
(expen…
net
GAAP
net $ 1,948.7 $ 1,460.0 $ 3,972.8 $ 3,660.3
income
Total
of GAAP
to
non-GA… 246.1 -282.0 920.4 -102.6
reconc…
items
above
Income
tax
effect
of GAAP -48.8 64.7 -170.6 37.0
to
non-GA…
reconc…
items
Income
tax
expens…
Shortf… 4.0 — 10.1 —
from
stock-…
compen…
Income
tax
expens…
Charge
related — 44.5 — 44.5
to
enactm…
of
OBBBA
Non-GA…
net $ 2,150.0 $ 1,287.2 $ 4,732.7 $ 3,639.2
income
Non-GA…
net
income $ 21.14 $ 12.42 $ 46.04 $ 34.63
per
share -
basic
Non-GA…
net
income $ 20.07 $ 11.83 $ 43.70 $ 32.87
per
share -
diluted
Shares
used in
calcul…
Non-GA…
net
income 101.7 103.6 102.8 105.1
per
share -
basic
Non-GA…
net
income 107.1 108.8 108.3 110.7
per
share -
diluted
14
RECONCILIATION OF GAAP TO NON-GAAP FINANCIAL INFORMATION (Unaudited) (continued)
Ef…
tax
ra…
re…
GA…
ETR
In…
tax
ef…
of
GA…
to
no…
re…
it…
In…
tax
ex…
Sh…
fr…
st…
co…
In…
tax
ex…
Ch…
re…
to
en…
of
OB…
No…
ETR
Gr…
ma…
on
net
pr…
sa…
re…
GA…
gr…
ma…
on
net
pr…
sa…
St…
co…
ex…
In…
as…
am…
ex…
Te…
ma…
in…
co…
No…
gr… 14.… 17.… 14.… 12.6%
ma… 0.4% (2.… 0.6% (0.8…
on (0.… —% (0.… —%
net —% 2025 (1.… Nine —% (0.9…
pr… Thr… 15.… Nine 13.… Mon… 14.… 10.9%
sa… Mon… 82% Mon… 82% End… 79% 82%
Fr… End… 2% End… 2% Sep… 2% 2%
ca… Sep… 2% Sep… 2% 30, 2% 2%
fl… 30, —% 30, —% 2026 3% —%
re… 2026 86% 2026 86% 2025 86% 2025 86%
──────────────────────────────────────────────────────────────────────────────
Net
ca…
pr… $ 3,6… $ 3,8…
by
op…
ac…
Ca… -77… -64…
ex…
Fr…
ca… $ 2,9… $ 3,1…
fl…
15
TABLE 4
REGENERON PHARMACEUTICALS, INC.
COLLABORATION REVENUE (Unaudited)
(In millions)
Three Nine
Months Months
Ended Ended
Sano… Septem… Septe…
coll… 30, 30,
reve… 2026 2025 2026 2025
──────────────────────────────────────────────────────────────────────────────
Rege…
share
of
prof…
in $ 2,574… $ 1,455.5 $ 6,058.3 $ 3,755…
conn…
with
comm…
of
anti…
Reim…
for
manu… 149.1 161.5 445.1 488.1
of
comm…
supp…
Total
Sano… 2,724… 1,617.0 6,503.4 4,243…
coll…
reve…
Bayer
coll…
reve…
Rege…
share
of
prof…
in
conn…
with
comm…
of 211.5 311.9 678.8 1,012…
EYLEA
8 mg
and
EYLEA
outs…
the
Unit…
Stat…
Reim…
for
manu… 55.3 32.9 151.5 91.1
of
comm…
supp…
Total
Bayer 266.8 344.8 830.3 1,103…
coll…
reve…
Other
coll… 9.7 6.6 21.5 12.8
reve…
Total
coll… $ 3,000… $ 1,968.4 $ 7,355.2 $ 5,360…
reve…
16
TABLE 5
REGENERON PHARMACEUTICALS, INC.
NET PRODUCT SALES OF REGENERON-DISCOVERED PRODUCTS (Unaudited)
(In millions)
T…
M…
E…
S… %
3… Ch…
2… 2… (T…
U… R… T… U… R… T… Sa…
──────────────────────────────────────────────────────────────────────────────
… $ 5… $ 1… $ 6… $ 3… $ 1… $ 4… 35 %
… $ 6… $ 3… $ 1… $ 4… $ 2… $ 6… 63 %
…
… $ 3… $ 2… $ 6… $ 6… $ 6… $ 1… (… %)
…
…
… $ 1… $ 6… $ 1… $ 1… $ 8… $ 1… (… %)
…
…
… $ 3… $ 1… $ 5… $ 2… $ 1… $ 3… 51 %
… $ 8… $ 1… $ 2… $ 6… $ 1… $ 2… 21 %
… $ 1… $ 6… $ 2… $ 1… $ 5… $ 1… 66 %
… $ 1… $ 0… $ 1… $ 0… $ — $ 0… *
… $ 5… $ 3… $ 9… $ 4… $ 2… $ 7… 28 %
…
N…
M…
E…
S…
3…
2… 2… %
Ch…
U… R… T… U… R… T… -T…
Sa…
… $ 1… $ 4… $ 1… $ 9… $ 3… $ 1… 35 %
… $ 1… $ 1… $ 2… $ 1… $ 6… $ 1… 63 %
…
… $ 1… $ 9… $ 2… $ 2… $ 2… $ 4… (… %)
…
…
… $ 3… $ 2… $ 5… $ 3… $ 2… $ 5… (… %)
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… $ 1… $ 4… $ 1… $ 6… $ 3… $ 1… 44 %
… $ 2… $ 5… $ 7… $ 1… $ 4… $ 6… 22 %
… $ 4… $ 1… $ 6… $ 2… $ 1… $ 4… 43 %
… $ 4… $ 1… $ 4… $ 0… $ — $ 0… *
… $ 1… $ 9… $ 2… $ 1… $ 8… $ 1… 43 %
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