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

9 Jul, 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 market share expected to expand due to recent label enhancements and anticipated prefilled syringe approval.

  • Lynozyfic, approved for late-line myeloma, shows strong early 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 in atopic dermatitis due to its dual mode of action, broad indications, and established efficacy and safety profile.

  • 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 further enhance its adoption.

  • Biosimilar competition is expected to drive declines in original EYLEA sales, but conversion to EYLEA HD and new patient uptake are mitigating factors.

Pipeline and future catalysts

  • Near-term catalysts include pivotal readouts for fianlimab plus Libtayo in metastatic melanoma, geographic atrophy, and PNH, all expected within the next 12-18 months.

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

  • Co-formulation of olatorepatide with Praluent 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 therapy, potentially doubling or more the addressable patient population.

  • Additional pipeline milestones include Factor XI pivotal data in VTE and competitor readouts that may impact strategic direction.

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