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Regeneron

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uuid000062c

Namestring
Regeneron
Legal namestring
Regeneron Pharmaceuticals, Inc.
Websiteurl
regeneron.com
Company typeenum
Public
Founded yearint
1988
Descriptiontext

Regeneron Pharmaceuticals is a public biopharmaceutical company (NASDAQ: REGN), founded in 1988 and headquartered in Tarrytown, New York, that discovers, develops, manufactures, and commercializes medicines for serious diseases. The company markets 15 approved or authorized therapies spanning ophthalmology (Eylea, Eylea HD), immunology and inflammatory disease (Dupixent via Sanofi collaboration), oncology (Libtayo), rare disease, and genetic medicine (Otarmeni, the first FDA-approved gene therapy for genetic hearing loss, received accelerated approval in April 2026). Its pipeline comprises roughly 50 candidates, with 2025 R&D investment of $5.9B and a broad focus that includes hematology, cardiovascular, neuroscience, and infectious disease.

The company's R&D engine is built on its proprietary VelociSuite® technology platform — including VelociGene® for genetic engineering, VelocImmune® for human antibody generation, and Veloci-T, Veloci-N, and related tools — which Regeneron uses internally and licenses to select partners. The Regeneron Genetics Center (RGC) is among the largest human sequencing efforts in industry, with 3M+ exomes sequenced and corresponding deidentified health records, generating data assets that feed target discovery and validation. Manufacturing is conducted in-house across multiple sites in the U.S. and Ireland.

Regeneron monetizes through direct product sales (Libtayo, Eylea franchise, Evkeeza, Inmazeb, etc.), profit-share and royalty arrangements with major partners (Sanofi for Dupixent and other antibodies, Bayer for Eylea outside the U.S., Roche for Ronapreve, Alnylam for cemdisiran), milestone payments, and technology licensing. Q1 2026 revenue was $3.6B (+19% YoY), with Dupixent profit share +42% and Eylea HD +52% YoY in that quarter. The end customer base spans patients, prescribers, payers, and government health systems across more than 100 countries, served via a combination of Regeneron's own specialty commercial infrastructure and partner-led distribution. The 10,000+ employee organization added a dedicated Global Capability Center in Hyderabad (announced May 2026) and a new Office of AI led by a Chief AI Officer (Divya Pathak) and Chief Digital & Technology Officer (Ryan Steinberger), reflecting an effort to scale digital and AI engineering alongside the core scientific enterprise.

Short descriptiontext

Regeneron Pharmaceuticals (NASDAQ: REGN) is a Tarrytown, NY-based biopharmaceutical company that uses its proprietary VelociSuite® antibody and genetics platform to discover, develop, manufacture, and commercialize 15 approved therapies across ophthalmology, immunology, oncology, and rare/genetic disease, serving patients globally via direct sales and major partner collaborations with Sanofi, Bayer, and others.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
5,001–10,000
akta.pro rankint
HeadquartersTarrytown, United States
HQ citystring
Tarrytown
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices8 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
monoclonal antibody therapies, biologic medicines development, genetic medicines platform, human antibody discovery, clinical biopharmaceutical research
NAICS code3 codes
  • Pharmaceutical and Medicine Manufacturing3254
  • Pharmaceutical Preparation Manufacturing325412
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code2 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Pharmaceutical Preparations2834
Product category
Biologic Pharmaceuticals
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model5 records
1Biologic product sales (Eylea franchise and other Regeneron-invented medicines)
TypeHardware Sales
Description

Regeneron commercializes 13 U.S. FDA-approved medicines and 10 EMA-authorized medicines, with 15 approved or authorized Regeneron-invented medicines available in over 100 countries. Q1 2026 reported 19% year-over-year revenue growth to $3.6 billion (driven significantly by Eylea HD growth of 52%, offsetting competitive pressure on the broader Eylea franchise including a 10% decline to $941 million in the prior quarter). Revenue model: one-time product sales of biologic therapies.

trefis.com
2Collaboration profit-sharing (Sanofi / Dupixent)
TypeLicensing Royalties
Description

Regeneron shares profits from the Sanofi collaboration for Dupixent (dupilumab), with Q1 2026 showing 42% growth in Regeneron's share of profits from this collaboration. Dupixent global net sales jumped 31%. This high-margin profit-sharing arrangement is expected to grow in 2H once the development cost repayment balance to Sanofi is fully paid off by mid-year, allowing Regeneron to capture its full share. Revenue model: profit-share / licensing-royalty hybrid.

trefis.com
3Out-licensing and royalty agreements
TypeLicensing Royalties
Description

Regeneron has executed 50+ new licensing and collaboration agreements over the past five years, including out-licensing of the IL-1 blocker (Arcalyst) to Kiniksa Pharmaceuticals (with Kiniksa reporting $213.4 million in Q1 2026 Arcalyst sales, 56% YoY growth) and global ophthalmology collaborations with Bayer. Includes access to Regeneron technologies & medicines for third-party studies. Revenue model: licensing-royalties.

regeneron.com
4Co-development R&D funding and milestone payments
TypeProfessional Services
Description

Strategic research collaborations with multiple partners — Intellia (CRISPR), Alnylam (RNAi, with multiple programs), BioNTech (immuno-oncology combinations), Sonoma Biotherapeutics (Treg cell therapy), Nykode (vaccines), Tessera (gene editing), and Hansoh (olatexopatide/HS-20094 for obesity) — provide upfront, milestone, and R&D funding. Revenue model: collaboration funding and milestones.

regeneron.com
5Government and institutional contracts (Ebola, public health preparedness)
TypeProfessional Services
Description

Regeneron has received WHO recommendation for its Ebola antibody (maftivimab/MBP134) for investigational use in Bundibugyo outbreak response and has donated up to 500 doses of Ebola treatment to the WHO for exclusive use in low- and lower-middle-income countries. Includes U.S. government and foundation funding (e.g., FNIH Biomarkers Consortium).

fool.com
Distribution channels10 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components6 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Supply Chain, Infrastructure
Pricing details1 tier
1Not publicly disclosed in source material; pricing approaches are designed for patient access and affordability per Regeneron's U.S. Pricing Philosophy.
ModelOtherBilling cadenceOther
Notes

Regeneron publishes a U.S. Pricing Philosophy and operates patient support programs serving more than 1.2 million eligible patients. Approximately $2.8B in medicines donated through patient assistance programs (2025 WAC basis).

regeneron.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 8 records shown
1Regeneron Genetics Center (RGC)
Description

One of the world's largest genomic databases, focused on human genetics-guided drug discovery with over 3 million sequenced exomes

regeneron.com
+7 more records
Core offering1 text field

Regeneron Pharmaceuticals is a fully integrated biopharmaceutical company that invents, develops, manufactures, and commercializes biologic medicines. It commercializes 13 U.S. FDA-approved, 10 EMA-authorized, and 7 PMDA-approved medicines across ophthalmology, immunology, oncology, rare diseases, cardiovascular, and infectious disease, with nearly 50 additional candidates in clinical development. Nearly 100% of product candidates are invented in-house and produced through the company's IOPS biologics manufacturing operations.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 17 values shown
  • 15 approved or authorized Regeneron-invented medicines in U.S. or other countries
+16 more records
Product overview1 text field

Regeneron is a fully integrated biopharmaceutical company offering a portfolio of 15 approved/authorized Regeneron-invented medicines (13 FDA-approved) rather than a single software product. The commercial portfolio spans ophthalmology (EYLEA / EYLEA HD, with Bayer), immunology (Dupixent, with Sanofi; Arcalyst/Kevzara), oncology (Libtayo, fianlimab, linvoseltamab, odronextamab), rare diseases (Otarmeni gene therapy for OTOF hearing loss; Lynozyfic/linvoseltamab for AL amyloidosis; Evkeeza for HoFH), cardiovascular (Praluent; REGN7508 Factor XI), infectious disease (REGEN-COV COVID-19 antibodies, Ebola maftivimab/MBP134), and investigational metabolic assets (olateforpatide, garetosmab, trevogrumab). Almost 100% of candidates are invented in-house and powered by the proprietary VelociSuite® antibody-discovery platform (VelociGene®, VelocImmune®) and the Regeneron Genetics Center® (RGC) — a wholly owned subsidiary with >3 million sequenced exomes that drives target discovery using machine learning, AI and large-scale analytics. The Internal Operations & Product Supply (IOPS) organization manufactures these biologics at the Rensselaer, NY and Limerick, Ireland sites, while a global commercial, R&D and — new in 2026 — Hyderabad Global Capability Centre (GCC) supports clinical operations, advanced data science, AI engineering and commercial analytics. Regeneron also operates the Regeneron Science Talent Search and Regeneron ISEF programs, and runs dozens of R&D collaborations (Sanofi, Bayer, Roche, Alnylam, Intellia, BioNTech, Sonoma, Nykode, CytomX, Parabilis, 2seventy bio, Decibel, Checkmate, etc.) that expand its antibody, cell therapy, gene therapy, gene editing and RNAi capabilities.

Product and service14 records
1EYLEA / EYLEA HD (aflibercept)
CategoryBiologic Medicine (Ophthalmology)
2Dupixent (dupilumab)
CategoryBiologic Medicine (Immunology)
3Libtayo (cemiplimab)
CategoryBiologic Medicine (Oncology)
4Otarmeni (lunsotogene parvec-cwha)
CategoryGene Therapy (Rare Disease)
5Lynozyfic (linvoseltamab)
CategoryBiologic Medicine (Oncology/Hematology)
6Arcalyst (rilonacept)
CategoryBiologic Medicine (Anti-Inflammatory)
7REGEN-COV / Ronapreve (casirivimab and imdevimab)
CategoryBiologic Medicine (Infectious Disease)
8Praluent (alirocumab)
CategoryBiologic Medicine (Cardiovascular)
9Kevzara (sarilumab)
CategoryBiologic Medicine (Immunology)
10Evkeeza (evinacumab)
CategoryBiologic Medicine (Cardiovascular Rare Disease)
11Maftivimab / MBP134 (Ebola antibody)
CategoryBiologic Medicine (Infectious Disease)
12VelociSuite® Technologies (VelociGene® and VelocImmune®)
CategoryProprietary Technology Platform
13Regeneron Genetics Center® (RGC) Research Services
CategoryGenomics Research Services
14Industrial Operations and Product Supply (IOPS) Biologics Manufacturing
CategoryBiologics Contract Manufacturing
Scale indicator20 records

Each record includes

Type, Value, Description, Source

Partnership22 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2024-01-30
Description

Regeneron acquired full development and commercialization rights to 2seventy bio's cell therapy pipeline. Acquisition included an upfront payment of $5 million and milestone payment for first major market approval. Led to formation of Regeneron Cell Medicines. Transaction expected to close in first half of 2024.

Strategic tierFlagship / CoreTypeStrategic or Co-development PartnerAnnounced on2023-08-09
Description

Acquisition completed Q3 2023 for approximately $109 million in cash (with potential additional payments if certain clinical milestones are achieved). Brought three gene therapy programs targeting congenital hearing loss in-house, including DB-OTO (now Otarmeni/lunsotogene parvec — the first FDA-approved gene therapy for genetic hearing loss).

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2022-04-19
Description

Regeneron acquired Checkmate Pharmaceuticals for approximately $250 million to expand its portfolio of investigational immune activator therapies.

Strategic tierFlagship / CoreTypeStrategic or Co-development Partner
Description

Long-standing antibody and immunotherapy collaboration. Most prominent component is the Dupixent (dupilumab) co-development and profit-sharing arrangement, which generated 42% growth in Regeneron's profit share in Q1 2026 alongside 31% growth in global Dupixent net sales. Also includes sarilumab (Kevzara) and itepekimab collaboration. Brook Jennings guided global launches of the first three Dupixent indications.

Strategic tierFlagship / CoreTypeStrategic or Co-development Partner
Description

Global ophthalmology collaboration partner. Co-promotes the Eylea franchise (Eylea and Eylea HD) outside the U.S. Eylea HD Q1 2026 sales surged 52%, while broader Eylea sales declined 10% to $941M.

Strategic tierFlagship / CoreTypeStrategic or Co-development Partner
Description

RNAi therapeutics collaboration covering multiple programs: ALN-APP (Alzheimer's), ALN-APOC3 (dyslipidemia), ALN-CFB (PNH), ALN-CIDEB (MASH), ALN-F1202 (Factor XII), ALN-HTT02 (Huntington's), ALN-PNP (MASLD), ALN-SNCA (Parkinson's), ALN-SOD (SOD1 ALS), ALN-ANG3 (diabetic kidney disease), and cemdisiran (C5 for gMG; FDA Priority Review target action date November 2026). Includes recent expansion of ALN-HSD (rapirosiran) for HSD17B13. Cemdisiran FDA priority review voucher used.

Strategic tierFlagship / CoreTypeStrategic or Co-development Partner
Description

Strategic R&D collaboration advancing CRISPR/Cas9 in vivo gene editing for genetic diseases. Co-developing nexiguran ziclumeran (NTLA-2001, "nex-z") for transthyretin amyloidosis (ATTR-CM and ATTRv-PN) — Phase 3 enrollment expected to complete in H2 2026. Intellia's lonvo-z (hereditary angioedema) submitted FDA BLA; Intellia also developing Nex-z in partnership with Regeneron.

Strategic tierFlagship / CoreTypeStrategic or Co-development Partner
Description

Since 2020, Regeneron and BioNTech have advanced a growing collaboration exploring synergistic immuno-oncology treatment combinations for several cancer types. Companies are advancing clinical development of Regeneron's homegrown PD-1 inhibitor in combination with BioNTech's FixVac mRNA vaccine candidate. Most recent agreement offers BioNTech the enhanced ability to pair Regeneron's PD-1 inhibitor broadly across their investigational portfolio.

Strategic tierFlagship / CoreTypeStrategic or Co-development Partner
Description

Global manufacturing and distribution collaboration for REGEN-COV (Regeneron's COVID-19 monoclonal antibody cocktail). The collaboration more than tripled manufacturing capacity and ultimately supplied millions of doses globally during the pandemic.

Strategic tierCoreTypeOEM/ Whitelabel/ Licensing Partner
Description

Regeneron granted Kiniksa an exclusive license to develop and commercialize Regeneron's IL-1 blocker (rilonacept/Arcalyst) — Regeneron's first FDA-approved therapy, originally approved in 2008 — in many countries around the world. Since the 2017 agreement, Kiniksa has led evaluation in IL-1α/IL-1β-mediated diseases. Arcalyst Q1 2026 sales $213.4M (+56% YoY); 2026 forecast $930-945M.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Treg cell therapy research, development and commercial collaboration. One of Regeneron's key cell therapy platform partnerships.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Vaccine collaboration. Part of Regeneron's broader exploration of vaccine technologies and combinations with Regeneron pipeline assets.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Research collaboration initially established in 2022 to develop next-generation conditionally-activated bispecific cancer immunotherapies. Expanded on June 3, 2026 with a $37 million target selection payment for two additional programs and option for six more future targets, bringing total potential milestone value to $4 billion. Combines CytomX's Probody® platform with Regeneron's Veloci-Bi technology.

Strategic tierFlagship / CoreTypeStrategic or Co-development Partner
Description

Strategic research collaboration announced May 18, 2026 to discover and develop multiple therapeutic candidates based on Parabilis' Helicon™ peptide platform, focused on Antibody-Helicon Conjugates (AHCs). Parabilis receives $125 million ($50M cash + $75M equity) with potential milestone payments of up to ~$2.2 billion plus tiered royalties. Regeneron also participated in Parabilis's $770.5M IPO via $75M private placement (June 2026). Total relationship value up to $2.3 billion.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Collaboration on TSRA-196 gene editing program for Alpha-1 Antitrypsin Disease. Part of Regeneron's gene editing expansion beyond the Intellia partnership.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Collaboration on olatorepatide (HS-20094) for obesity — a GLP-1/GIP receptor agonist. 48-week Chinese study with 604 patients showed up to 19% weight loss; Regeneron plans to begin Phase 3 trials in 2025.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Biomarkers Consortium partner. Long-standing relationship for biomarker discovery and validation to support clinical development.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Long-standing RGC collaboration via the MyCode Community Health Initiative, which has enrolled 150,000+ volunteers who are notified if genetic changes associated with treatable conditions are found. The story of Barbara Barnes is a notable example of the program's impact.

19U.S. Government / TrumpRx
Strategic tierCoreTypeGTM or Marketing Partner
Description

Engagement with the TrumpRx drug pricing platform — a U.S. government initiative listing more than 750 medications (including Regeneron products) to encourage cost-effective purchasing. Projected to save Americans over $500 billion over the next decade through most-favoured-nation agreements. Regeneron also participated in HHS/FDA National Priority Voucher program (Otarmeni approved under it).

fool.com
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Regeneron's Ebola antibody (maftivimab) has been recommended by WHO for investigational use in response to the current Bundibugyo Ebolavirus outbreak in the Democratic Republic of Congo. Regeneron has donated up to 500 doses of Ebola treatment to the WHO for exclusive use in low- and lower-middle-income countries.

Strategic tierCoreTypeTechnology or Integration
Description

Technology partnership for AI-driven enterprise process automation. Regeneron won an Appian 2026 North American Innovation Award at Appian World in Orlando, FL for embedding AI into core enterprise processes to achieve measurable business outcomes. Judged by IDC and Appian executives.

22Educational and nonprofit grant recipients (AMA, ACCME, OIG, PhRMA-adjacent organizations)
Strategic tierPeripheralTypeOthers
Description

Regeneron operates four funding portals: Corporate funding application (patient advocacy groups, medical societies, STEM education, community-based organizations), Educational funding (CME, non-CME, academic fellowship, conference funding), Sponsorships & exhibits, and Third-party research requests. All interactions comply with AMA, ACCME, PhRMA, FDA, and OIG guidelines.

regeneron.com
Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight7 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Large-cap biotech with a similarly broad biologics platform spanning antibodies, bispecifics (BiTE), and large-scale manufacturing. Amgen competes with Regeneron in ophthalmology indirectly and overlaps in oncology/immunology biologics manufacturing and pipeline breadth.

TypeDirect peer
Description

Innovative mid-to-large biotech focused on serious diseases (CF, sickle cell, pain) with a comparable 'science-driven in-house discovery + collaboration' model. Vertex's Casgevy (CRISPR gene editing) directly parallels Regeneron's nexiguran ziclumeran gene-editing program in modality and rare-disease focus.

TypeBroad incumbent
Description

Mature biotech with strong commercial franchises (HIV, oncology) and growing investment in cell therapy and antibody-drug conjugates. Gilead is a relevant comparable for Regeneron's commercial scale and oncology/hematology pipeline.

TypeBroad incumbent
Description

Major pharma with overlapping immunology and oncology biologics portfolios (PD-1 inhibitors, LAG-3 via Opdualag). BMS competes directly with Regeneron in immuno-oncology (nivolumab vs. cemiplimab) and immunology franchises.

TypeDirect peer
Description

Regeneron's largest collaborator (Dupixent, itepekimab, sarilumab) and a global immunology leader (Dupixent, Dupixent follow-ons). Sanofi is simultaneously partner and direct competitor in inflammation/immunology biologics.

TypeBroad incumbent
Description

Immunology incumbent (Humira, Skyrizi, Rinvoq) competing head-to-head with Dupixent in atopic dermatitis, IBD, and other indications. Comparable R&D scale and immunology pipeline depth make AbbVie a key commercial and pipeline benchmark.

TypeDirect peer
Description

Antibody-platform specialist (bispecifics, antibody-drug conjugates) with a similar in-house platform-plus-collaboration model (e.g., Darzalex with Janssen). Genmab directly parallels Regeneron's bispecific antibody pipeline.

TypeEmerging player
Description

RNAi therapeutics pioneer and Regeneron's closest genetic-medicines modality partner (cemdisiran, ALN-HSD, ALN-APP, ALN-CFB, etc.). Comparable in modality focus and genetic-medicines pipeline depth.

TypeEmerging player
Description

mRNA and immuno-oncology partner with Regeneron (PD-1 + FixVac combinations). BioNTech is a relevant comparable for next-gen oncology biologics and Regeneron's broader cell/vaccine collaborations.

TypeEmerging player
Description

mRNA-based biotech expanding from COVID-19 vaccines into oncology and rare disease. Comparable to Regeneron in pioneering a genetic-medicines platform, large-scale manufacturing footprint, and pipeline breadth outside its original franchise.

Market position
Strengths4 records

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Headline, Details, Source

Weaknesses4 records

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Headline, Details, Source

Competitive moat6 records

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Type, Details

Key risks6 records

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Key highlights7 records

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Headline, Details, Source

Customer concentration

Classification, Details

Named customers18 records

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Name, Industry, Type, Use case, Source, UUID

Ideal customer profile4 records

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Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

Integration12 records

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Title, Type, Description, Source

AI capability10 records

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Type, Description, Source

AI maturity
App detail

Has app

Feature7 records

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Title, Differentiator, Description, Source

Core technology
Revenue estimate
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Number of profiles
Profiles14 records

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Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries4 records

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Name, Acquired on, Relationship type, Type, Business focus

Compliance15 records

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Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds3 records

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Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors1 record

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Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A4 records

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Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment14 records

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Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Regeneron

Biologic Pharmaceuticalsregeneron.com

Regeneron Pharmaceuticals (NASDAQ: REGN) is a Tarrytown, NY-based biopharmaceutical company that uses its proprietary VelociSuite® antibody and genetics platform to discover, develop, manufacture, and commercialize 15 approved therapies across ophthalmology, immunology, oncology, and rare/genetic disease, serving patients globally via direct sales and major partner collaborations with Sanofi, Bayer, and others.

What Regeneron does

Regeneron Pharmaceuticals is a public biopharmaceutical company (NASDAQ: REGN), founded in 1988 and headquartered in Tarrytown, New York, that discovers, develops, manufactures, and commercializes medicines for serious diseases. The company markets 15 approved or authorized therapies spanning ophthalmology (Eylea, Eylea HD), immunology and inflammatory disease (Dupixent via Sanofi collaboration), oncology (Libtayo), rare disease, and genetic medicine (Otarmeni, the first FDA-approved gene therapy for genetic hearing loss, received accelerated approval in April 2026). Its pipeline comprises roughly 50 candidates, with 2025 R&D investment of $5.9B and a broad focus that includes hematology, cardiovascular, neuroscience, and infectious disease.

The company's R&D engine is built on its proprietary VelociSuite® technology platform — including VelociGene® for genetic engineering, VelocImmune® for human antibody generation, and Veloci-T, Veloci-N, and related tools — which Regeneron uses internally and licenses to select partners. The Regeneron Genetics Center (RGC) is among the largest human sequencing efforts in industry, with 3M+ exomes sequenced and corresponding deidentified health records, generating data assets that feed target discovery and validation. Manufacturing is conducted in-house across multiple sites in the U.S. and Ireland.

Regeneron monetizes through direct product sales (Libtayo, Eylea franchise, Evkeeza, Inmazeb, etc.), profit-share and royalty arrangements with major partners (Sanofi for Dupixent and other antibodies, Bayer for Eylea outside the U.S., Roche for Ronapreve, Alnylam for cemdisiran), milestone payments, and technology licensing. Q1 2026 revenue was $3.6B (+19% YoY), with Dupixent profit share +42% and Eylea HD +52% YoY in that quarter. The end customer base spans patients, prescribers, payers, and government health systems across more than 100 countries, served via a combination of Regeneron's own specialty commercial infrastructure and partner-led distribution. The 10,000+ employee organization added a dedicated Global Capability Center in Hyderabad (announced May 2026) and a new Office of AI led by a Chief AI Officer (Divya Pathak) and Chief Digital & Technology Officer (Ryan Steinberger), reflecting an effort to scale digital and AI engineering alongside the core scientific enterprise.

Regeneron firmographics

Firmographics
Name
Regeneron
Legal name
Regeneron Pharmaceuticals, Inc.
Website
https://regeneron.com
Company type
Public
Founded year
1988
Operating status
Operating
Headcount range
5,001–10,000 employees
Short description
Regeneron Pharmaceuticals (NASDAQ: REGN) is a Tarrytown, NY-based biopharmaceutical company that uses its proprietary VelociSuite® antibody and genetics platform to discover, develop, manufacture, and commercialize 15 approved therapies across ophthalmology, immunology, oncology, and rare/genetic disease, serving patients globally via direct sales and major partner collaborations with Sanofi, Bayer, and others.
Ownership category
akta.pro rank

Where Regeneron is headquartered

Location

Headquarters

HQ city
Tarrytown
HQ country
United States
HQ region
North America

Offices8 records

Markets served

Regeneron business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Operations, Marketing or Sales, Supply Chain, Infrastructure

Revenue model

  1. Biologic product sales (Eylea franchise and other Regeneron-invented medicines): Regeneron commercializes 13 U.S. FDA-approved medicines and 10 EMA-authorized medicines, with 15 approved or authorized Regeneron-invented medicines available in over 100 countries. Q1 2026 reported 19% year-over-year revenue growth to $3.6 billion (driven significantly by Eylea HD growth of 52%, offsetting competitive pressure on the broader Eylea franchise including a 10% decline to $941 million in the prior quarter). Revenue model: one-time product sales of biologic therapies.
  2. Collaboration profit-sharing (Sanofi / Dupixent): Regeneron shares profits from the Sanofi collaboration for Dupixent (dupilumab), with Q1 2026 showing 42% growth in Regeneron's share of profits from this collaboration. Dupixent global net sales jumped 31%. This high-margin profit-sharing arrangement is expected to grow in 2H once the development cost repayment balance to Sanofi is fully paid off by mid-year, allowing Regeneron to capture its full share. Revenue model: profit-share / licensing-royalty hybrid.
  3. Out-licensing and royalty agreements: Regeneron has executed 50+ new licensing and collaboration agreements over the past five years, including out-licensing of the IL-1 blocker (Arcalyst) to Kiniksa Pharmaceuticals (with Kiniksa reporting $213.4 million in Q1 2026 Arcalyst sales, 56% YoY growth) and global ophthalmology collaborations with Bayer. Includes access to Regeneron technologies & medicines for third-party studies. Revenue model: licensing-royalties.
  4. Co-development R&D funding and milestone payments: Strategic research collaborations with multiple partners — Intellia (CRISPR), Alnylam (RNAi, with multiple programs), BioNTech (immuno-oncology combinations), Sonoma Biotherapeutics (Treg cell therapy), Nykode (vaccines), Tessera (gene editing), and Hansoh (olatexopatide/HS-20094 for obesity) — provide upfront, milestone, and R&D funding. Revenue model: collaboration funding and milestones.
  5. Government and institutional contracts (Ebola, public health preparedness): Regeneron has received WHO recommendation for its Ebola antibody (maftivimab/MBP134) for investigational use in Bundibugyo outbreak response and has donated up to 500 doses of Ebola treatment to the WHO for exclusive use in low- and lower-middle-income countries. Includes U.S. government and foundation funding (e.g., FNIH Biomarkers Consortium).

Pricing tiers

ModelBillingPrice
OtherOtherNot publicly disclosed in source material; pricing approaches are designed for patient access and affordability per Regeneron's U.S. Pricing Philosophy.

Go-to-market motion3 records

Distribution channels10 records

Regeneron product offering

Product offering

Core offering

Regeneron Pharmaceuticals is a fully integrated biopharmaceutical company that invents, develops, manufactures, and commercializes biologic medicines. It commercializes 13 U.S. FDA-approved, 10 EMA-authorized, and 7 PMDA-approved medicines across ophthalmology, immunology, oncology, rare diseases, cardiovascular, and infectious disease, with nearly 50 additional candidates in clinical development. Nearly 100% of product candidates are invented in-house and produced through the company's IOPS biologics manufacturing operations.

Product overview

Regeneron is a fully integrated biopharmaceutical company offering a portfolio of 15 approved/authorized Regeneron-invented medicines (13 FDA-approved) rather than a single software product. The commercial portfolio spans ophthalmology (EYLEA / EYLEA HD, with Bayer), immunology (Dupixent, with Sanofi; Arcalyst/Kevzara), oncology (Libtayo, fianlimab, linvoseltamab, odronextamab), rare diseases (Otarmeni gene therapy for OTOF hearing loss; Lynozyfic/linvoseltamab for AL amyloidosis; Evkeeza for HoFH), cardiovascular (Praluent; REGN7508 Factor XI), infectious disease (REGEN-COV COVID-19 antibodies, Ebola maftivimab/MBP134), and investigational metabolic assets (olateforpatide, garetosmab, trevogrumab). Almost 100% of candidates are invented in-house and powered by the proprietary VelociSuite® antibody-discovery platform (VelociGene®, VelocImmune®) and the Regeneron Genetics Center® (RGC) — a wholly owned subsidiary with >3 million sequenced exomes that drives target discovery using machine learning, AI and large-scale analytics. The Internal Operations & Product Supply (IOPS) organization manufactures these biologics at the Rensselaer, NY and Limerick, Ireland sites, while a global commercial, R&D and — new in 2026 — Hyderabad Global Capability Centre (GCC) supports clinical operations, advanced data science, AI engineering and commercial analytics. Regeneron also operates the Regeneron Science Talent Search and Regeneron ISEF programs, and runs dozens of R&D collaborations (Sanofi, Bayer, Roche, Alnylam, Intellia, BioNTech, Sonoma, Nykode, CytomX, Parabilis, 2seventy bio, Decibel, Checkmate, etc.) that expand its antibody, cell therapy, gene therapy, gene editing and RNAi capabilities.

Differentiator

Problem solved

Functional benefit

Brands

  • Regeneron Genetics Center (RGC): One of the world's largest genomic databases, focused on human genetics-guided drug discovery with over 3 million sequenced exomes
  • Regeneron Cell Medicines
  • VelociSuite
  • IOPS (Industrial Operations and Product Supply)
  • Regeneron Science Talent Search (STS)
  • Regeneron International Science and Engineering Fair (ISEF)
  • Eylea (aflibercept) / Eylea HD
  • Libtayo (cemiplimab)

Products and services

  • EYLEA / EYLEA HD (aflibercept)
  • Dupixent (dupilumab)
  • Libtayo (cemiplimab)
  • Otarmeni (lunsotogene parvec-cwha)
  • Lynozyfic (linvoseltamab)
  • Arcalyst (rilonacept)
  • REGEN-COV / Ronapreve (casirivimab and imdevimab)
  • Praluent (alirocumab)
  • Kevzara (sarilumab)
  • Evkeeza (evinacumab)
  • Maftivimab / MBP134 (Ebola antibody)
  • VelociSuite® Technologies (VelociGene® and VelocImmune®)
  • Regeneron Genetics Center® (RGC) Research Services
  • Industrial Operations and Product Supply (IOPS) Biologics Manufacturing

Quantifiable outcome

  • 15 approved or authorized Regeneron-invented medicines in U.S. or other countries
  • +16 more outcomes

Companies that use Regeneron

Customer profile

Named customers18 records

Ideal customer profiles4 records

Regeneron technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Integration12 records

AI capability10 records

Feature7 records

Regeneron partnerships and signals

Strategic signal

Partnerships

22 partnerships are on record, tiered core, flagship / core and peripheral.

  • 2seventy biocoreStrategic or Co-development Partner · 30 January 2024Regeneron acquired full development and commercialization rights to 2seventy bio's cell therapy pipeline. Acquisition included an upfront payment of $5 million and milestone payment for first major market approval. Led to formation of Regeneron Cell Medicines. Transaction expected to close in first half of 2024.
  • Decibel Therapeuticsflagship / coreStrategic or Co-development Partner · 9 August 2023Acquisition completed Q3 2023 for approximately $109 million in cash (with potential additional payments if certain clinical milestones are achieved). Brought three gene therapy programs targeting congenital hearing loss in-house, including DB-OTO (now Otarmeni/lunsotogene parvec — the first FDA-approved gene therapy for genetic hearing loss).
  • Checkmate PharmaceuticalscoreStrategic or Co-development Partner · 19 April 2022Regeneron acquired Checkmate Pharmaceuticals for approximately $250 million to expand its portfolio of investigational immune activator therapies.
  • Sanofiflagship / coreStrategic or Co-development PartnerLong-standing antibody and immunotherapy collaboration. Most prominent component is the Dupixent (dupilumab) co-development and profit-sharing arrangement, which generated 42% growth in Regeneron's profit share in Q1 2026 alongside 31% growth in global Dupixent net sales. Also includes sarilumab (Kevzara) and itepekimab collaboration. Brook Jennings guided global launches of the first three Dupixent indications.
  • Bayerflagship / coreStrategic or Co-development PartnerGlobal ophthalmology collaboration partner. Co-promotes the Eylea franchise (Eylea and Eylea HD) outside the U.S. Eylea HD Q1 2026 sales surged 52%, while broader Eylea sales declined 10% to $941M.
  • Alnylam Pharmaceuticalsflagship / coreStrategic or Co-development PartnerRNAi therapeutics collaboration covering multiple programs: ALN-APP (Alzheimer's), ALN-APOC3 (dyslipidemia), ALN-CFB (PNH), ALN-CIDEB (MASH), ALN-F1202 (Factor XII), ALN-HTT02 (Huntington's), ALN-PNP (MASLD), ALN-SNCA (Parkinson's), ALN-SOD (SOD1 ALS), ALN-ANG3 (diabetic kidney disease), and cemdisiran (C5 for gMG; FDA Priority Review target action date November 2026). Includes recent expansion of ALN-HSD (rapirosiran) for HSD17B13. Cemdisiran FDA priority review voucher used.
  • Intellia Therapeuticsflagship / coreStrategic or Co-development PartnerStrategic R&D collaboration advancing CRISPR/Cas9 in vivo gene editing for genetic diseases. Co-developing nexiguran ziclumeran (NTLA-2001, "nex-z") for transthyretin amyloidosis (ATTR-CM and ATTRv-PN) — Phase 3 enrollment expected to complete in H2 2026. Intellia's lonvo-z (hereditary angioedema) submitted FDA BLA; Intellia also developing Nex-z in partnership with Regeneron.
  • BioNTechflagship / coreStrategic or Co-development PartnerSince 2020, Regeneron and BioNTech have advanced a growing collaboration exploring synergistic immuno-oncology treatment combinations for several cancer types. Companies are advancing clinical development of Regeneron's homegrown PD-1 inhibitor in combination with BioNTech's FixVac mRNA vaccine candidate. Most recent agreement offers BioNTech the enhanced ability to pair Regeneron's PD-1 inhibitor broadly across their investigational portfolio.
  • Rocheflagship / coreStrategic or Co-development PartnerGlobal manufacturing and distribution collaboration for REGEN-COV (Regeneron's COVID-19 monoclonal antibody cocktail). The collaboration more than tripled manufacturing capacity and ultimately supplied millions of doses globally during the pandemic.
  • Kiniksa PharmaceuticalscoreOEM/ Whitelabel/ Licensing PartnerRegeneron granted Kiniksa an exclusive license to develop and commercialize Regeneron's IL-1 blocker (rilonacept/Arcalyst) — Regeneron's first FDA-approved therapy, originally approved in 2008 — in many countries around the world. Since the 2017 agreement, Kiniksa has led evaluation in IL-1α/IL-1β-mediated diseases. Arcalyst Q1 2026 sales $213.4M (+56% YoY); 2026 forecast $930-945M.
  • Sonoma BiotherapeuticscoreStrategic or Co-development PartnerTreg cell therapy research, development and commercial collaboration. One of Regeneron's key cell therapy platform partnerships.
  • Nykode TherapeuticscoreStrategic or Co-development PartnerVaccine collaboration. Part of Regeneron's broader exploration of vaccine technologies and combinations with Regeneron pipeline assets.
  • CytomX TherapeuticscoreStrategic or Co-development PartnerResearch collaboration initially established in 2022 to develop next-generation conditionally-activated bispecific cancer immunotherapies. Expanded on June 3, 2026 with a $37 million target selection payment for two additional programs and option for six more future targets, bringing total potential milestone value to $4 billion. Combines CytomX's Probody® platform with Regeneron's Veloci-Bi technology.
  • Parabilis Medicines (formerly FogPharma)flagship / coreStrategic or Co-development PartnerStrategic research collaboration announced May 18, 2026 to discover and develop multiple therapeutic candidates based on Parabilis' Helicon™ peptide platform, focused on Antibody-Helicon Conjugates (AHCs). Parabilis receives $125 million ($50M cash + $75M equity) with potential milestone payments of up to ~$2.2 billion plus tiered royalties. Regeneron also participated in Parabilis's $770.5M IPO via $75M private placement (June 2026). Total relationship value up to $2.3 billion.
  • Tessera TherapeuticscoreStrategic or Co-development PartnerCollaboration on TSRA-196 gene editing program for Alpha-1 Antitrypsin Disease. Part of Regeneron's gene editing expansion beyond the Intellia partnership.
  • Hansoh Pharmaceutical GroupcoreStrategic or Co-development PartnerCollaboration on olatorepatide (HS-20094) for obesity — a GLP-1/GIP receptor agonist. 48-week Chinese study with 604 patients showed up to 19% weight loss; Regeneron plans to begin Phase 3 trials in 2025.
  • Foundation for the National Institutes of Health (FNIH)coreStrategic or Co-development PartnerBiomarkers Consortium partner. Long-standing relationship for biomarker discovery and validation to support clinical development.
  • Geisinger Health System (MyCode Community Health Initiative)coreStrategic or Co-development PartnerLong-standing RGC collaboration via the MyCode Community Health Initiative, which has enrolled 150,000+ volunteers who are notified if genetic changes associated with treatable conditions are found. The story of Barbara Barnes is a notable example of the program's impact.
  • U.S. Government / TrumpRxcoreGTM or Marketing PartnerEngagement with the TrumpRx drug pricing platform — a U.S. government initiative listing more than 750 medications (including Regeneron products) to encourage cost-effective purchasing. Projected to save Americans over $500 billion over the next decade through most-favoured-nation agreements. Regeneron also participated in HHS/FDA National Priority Voucher program (Otarmeni approved under it).
  • World Health Organization (WHO)coreStrategic or Co-development PartnerRegeneron's Ebola antibody (maftivimab) has been recommended by WHO for investigational use in response to the current Bundibugyo Ebolavirus outbreak in the Democratic Republic of Congo. Regeneron has donated up to 500 doses of Ebola treatment to the WHO for exclusive use in low- and lower-middle-income countries.
  • AppiancoreTechnology or IntegrationTechnology partnership for AI-driven enterprise process automation. Regeneron won an Appian 2026 North American Innovation Award at Appian World in Orlando, FL for embedding AI into core enterprise processes to achieve measurable business outcomes. Judged by IDC and Appian executives.
  • Educational and nonprofit grant recipients (AMA, ACCME, OIG, PhRMA-adjacent organizations)peripheralOthersRegeneron operates four funding portals: Corporate funding application (patient advocacy groups, medical societies, STEM education, community-based organizations), Educational funding (CME, non-CME, academic fellowship, conference funding), Sponsorships & exhibits, and Third-party research requests. All interactions comply with AMA, ACCME, PhRMA, FDA, and OIG guidelines.

Scale indicators20 records

Recent moves6 records

Expansion highlights7 records

Regeneron competitors and assessment

Company assessment

Direct peers

  • Amgen: Large-cap biotech with a similarly broad biologics platform spanning antibodies, bispecifics (BiTE), and large-scale manufacturing. Amgen competes with Regeneron in ophthalmology indirectly and overlaps in oncology/immunology biologics manufacturing and pipeline breadth.
  • Vertex Pharmaceuticals: Innovative mid-to-large biotech focused on serious diseases (CF, sickle cell, pain) with a comparable 'science-driven in-house discovery + collaboration' model. Vertex's Casgevy (CRISPR gene editing) directly parallels Regeneron's nexiguran ziclumeran gene-editing program in modality and rare-disease focus.
  • Sanofi: Regeneron's largest collaborator (Dupixent, itepekimab, sarilumab) and a global immunology leader (Dupixent, Dupixent follow-ons). Sanofi is simultaneously partner and direct competitor in inflammation/immunology biologics.
  • Genmab: Antibody-platform specialist (bispecifics, antibody-drug conjugates) with a similar in-house platform-plus-collaboration model (e.g., Darzalex with Janssen). Genmab directly parallels Regeneron's bispecific antibody pipeline.

Broad incumbents

  • Gilead Sciences: Mature biotech with strong commercial franchises (HIV, oncology) and growing investment in cell therapy and antibody-drug conjugates. Gilead is a relevant comparable for Regeneron's commercial scale and oncology/hematology pipeline.
  • Bristol-Myers Squibb: Major pharma with overlapping immunology and oncology biologics portfolios (PD-1 inhibitors, LAG-3 via Opdualag). BMS competes directly with Regeneron in immuno-oncology (nivolumab vs. cemiplimab) and immunology franchises.
  • AbbVie: Immunology incumbent (Humira, Skyrizi, Rinvoq) competing head-to-head with Dupixent in atopic dermatitis, IBD, and other indications. Comparable R&D scale and immunology pipeline depth make AbbVie a key commercial and pipeline benchmark.

Emerging players

  • Alnylam Pharmaceuticals: RNAi therapeutics pioneer and Regeneron's closest genetic-medicines modality partner (cemdisiran, ALN-HSD, ALN-APP, ALN-CFB, etc.). Comparable in modality focus and genetic-medicines pipeline depth.
  • BioNTech: mRNA and immuno-oncology partner with Regeneron (PD-1 + FixVac combinations). BioNTech is a relevant comparable for next-gen oncology biologics and Regeneron's broader cell/vaccine collaborations.
  • Moderna: mRNA-based biotech expanding from COVID-19 vaccines into oncology and rare disease. Comparable to Regeneron in pioneering a genetic-medicines platform, large-scale manufacturing footprint, and pipeline breadth outside its original franchise.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat6 records

Key risks6 records

Key highlights7 records

Customer concentration

Regeneron social profiles

Digital presence

Regeneron compliance and trust

Trust signal

Compliance15 records

Regeneron financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Regeneron leadership team

Management profile

Number of profiles

Profiles14 records

Regeneron subsidiaries and ownership

Company hierarchy

Subsidiaries4 records

Regeneron funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors1 record

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Regeneron M&A and investment

M&A and investment

M&A4 records

Investments14 records

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Regeneron

What does Regeneron do?

Regeneron Pharmaceuticals is a fully integrated biopharmaceutical company that invents, develops, manufactures, and commercializes biologic medicines. It commercializes 13 U.S. FDA-approved, 10 EMA-authorized, and 7 PMDA-approved medicines across ophthalmology, immunology, oncology, rare diseases, cardiovascular, and infectious disease, with nearly 50 additional candidates in clinical development. Nearly 100% of product candidates are invented in-house and produced through the company's IOPS biologics manufacturing operations.

Is Regeneron a public or private company?

Regeneron is a public company. It is classified as public and is currently operating.

When was Regeneron founded?

Regeneron was founded in 1988. It employs 5,001 to 10,000 people.

Where is Regeneron based?

Regeneron is headquartered in Tarrytown, United States, in the North America region.

How does Regeneron make money?

Five revenue lines are on record. Biologic product sales (Eylea franchise and other Regeneron-invented medicines) is the primary driver. The others are collaboration profit-sharing (Sanofi / Dupixent), out-licensing and royalty agreements, co-development R&D funding and milestone payments and government and institutional contracts (Ebola, public health preparedness).

Who are Regeneron's main competitors?

Direct peers on record are Amgen, Vertex Pharmaceuticals, Sanofi and Genmab. Broad incumbents are Gilead Sciences, Bristol-Myers Squibb and AbbVie. Emerging players are Alnylam Pharmaceuticals, BioNTech and Moderna.

Does Regeneron have an API?

No public API is recorded for Regeneron.

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Live signals
MarketWatchRegeneron Pharmaceuticals Inc. stock outperforms competitors on strong trading dayRegeneron Pharmaceuticals stock rose 1.69% to $738.72 on Tuesday, outperforming the broader market. The stock closed 14.04% below its 52-week high of $859.34, which was reached on September 3rd.MarketScreenerRegeneron Pharmaceuticals, Inc. Announces Presentation of New Clinical Research At European Society for Medical Oncology Congress 2026Regeneron Pharmaceuticals will present 10 new clinical research abstracts at the ESMO Congress 2026 in Madrid, covering trials in CSCC, NSCLC, ovarian cancer, melanoma, and cancer-associated thrombosis. The data includes potential uses of neoadjuvant Libtayo and other investigational therapies, with safety and efficacy not yet evaluated by regulatory authorities.Seeking AlphaRegeneron sees nearly $0.18 per share earnings headwind (REGN)Regeneron disclosed a Q3 2026 net income per diluted share headwind of about $0.18 from a pre-tax R&D charge of roughly $22M. The charge stems from asset acquisitions and upfront payments for collaboration and licensing agreements. The company also expanded its collaboration with Sanofi, with a deal worth up to $8B.American Banking and Market NewsRegeneron Pharmaceuticals (NASDAQ:REGN) Price Target Raised to $950.00JPMorgan raised Regeneron's price target to $950 from $900, citing an overweight rating. The stock rose 1.2% to $735.01, and Regeneron reported Q2 EPS of $14.29, beating estimates of $10.16. Analysts project 45.34 EPS for the current year.American Banking and Market NewsRegeneron Pharmaceuticals, Inc. $REGN Stock Bought by Central Pacific Bank Trust DivisionCentral Pacific Bank Trust Division increased its Regeneron Pharmaceuticals stake by 90.3% in Q3, buying 1,275 shares. Regeneron reported Q2 EPS of $14.29, beating estimates, and declared a $0.94 quarterly dividend. Analysts rate the stock a Moderate Buy with a consensus price target of $809.50.FinanzNachrichten.deKampf gegen Hautkrebs: Wie Vidac Pharma, Biofrontera und Regeneron an verschiedenen Stellen ansetzenAt a European dermatology conference in Vienna, new approaches to treating large skin wounds were presented, shifting focus to stopping skin cancer before it spreads. The article highlights Vidac Pharma, Biofrontera, and Regeneron as companies addressing this, with stock tickers provided.AD HOC NEWSSanofi Aktie: Patentklippe droht trotz Regeneron-DealSanofi's partnership with Regeneron adds development projects but fails to fully offset patent cliffs, leaving the company dependent on Dupixent. The deal includes a $1B upfront payment and up to $7B in milestones, while the stock has fallen 16% since year start. Investors await Q3 results on October 30, 2026.MarketWatchRegeneron Pharmaceuticals Inc. stock underperforms Monday when compared to competitorsRegeneron Pharmaceuticals closed 15.46% below its 52-week high of $859.34 on Monday, underperforming Amgen, Moderna, and Gilead. Trading volume was 68,774 below its 50-day average. The stock's decline was not explained.American Banking and Market NewsSanofi, Regeneron Expand DUPIXENT Alliance in Deal Worth Up to €8 BillionSanofi and Regeneron expanded their DUPIXENT alliance, with Regeneron contributing four antibody programs targeting IL-4 and IL-13. Sanofi will pay €1 billion upfront and up to €7 billion more on milestones, splitting development costs and profits equally. Registrational studies for the lead asset are planned for late 2027 or early 2028.American Banking and Market NewsJefferies Financial Group Forecasts Strong Price Appreciation for Regeneron Pharmaceuticals (NASDAQ:REGN) StockJefferies raised its price target on Regeneron Pharmaceuticals to $930 from $870, maintaining a buy rating. The stock opened at $735.20, with a consensus price target of $809.50. Analysts predict 45.34 EPS for the current fiscal year.