Barclays 28th Annual Global Healthcare Conference
Logotype for Regeneron Pharmaceuticals Inc

Regeneron Pharmaceuticals (REGN) Barclays 28th Annual Global Healthcare Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for Regeneron Pharmaceuticals Inc

Barclays 28th Annual Global Healthcare Conference summary

10 Mar, 2026

Key product performance and launches

  • Dupixent achieved $17.8 billion in sales last year, up 32% year-over-year, with continued growth across all nine FDA-approved indications, including recent launches in chronic spontaneous urticaria and COPD.

  • COPD launch for Dupixent is progressing well, with robust payer coverage and strong enthusiasm from pulmonologists, improving patient outcomes and quality of life.

  • EYLEA HD now represents nearly half of the EYLEA franchise revenues, with recent FDA label enhancements and anticipated prefilled syringe approval expected to further boost market share.

  • Lynozyfic, approved for late-line myeloma, is showing early positive uptake and is being evaluated for broader use in earlier lines and precursor conditions.

Competitive positioning and life cycle management

  • Dupixent maintains a strong competitive edge due to its dual mode of action, broad indications, and established efficacy and safety profile, with ongoing monitoring of emerging competition.

  • Life cycle management for Dupixent includes development of long-acting IL-4 and IL-13 antibodies, aiming for less frequent dosing and continued market leadership.

  • EYLEA HD is positioned as the most flexible and durable anti-VEGF therapy, with the prefilled syringe expected to drive further adoption.

  • EYLEA is expected to see sequential declines due to biosimilar competition, but conversion efforts are underway to transition patients to EYLEA HD.

Pipeline and future catalysts

  • Near-term catalysts include pivotal readouts for fianlimab plus Libtayo in metastatic melanoma, geographic atrophy, and PNH, with key data expected throughout this year.

  • Obesity program with olatorepatide demonstrated 19% weight loss in pivotal China data, with U.S. and ex-China Phase III studies planned to start later this year.

  • Co-formulation of olatorepatide with alirocumab aims to address both weight loss and LDL cholesterol reduction, targeting an unmet need in the obesity market.

  • Lynozyfic's opportunity could expand significantly as it moves into earlier lines of myeloma, with the U.S. patient population doubling from fourth-line to third-line settings.

  • Additional pipeline milestones include Factor XI pivotal data in VTE expected in the first half of next year and ongoing progress in geographic atrophy and PNH.

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