Regeneron Pharmaceuticals, Inc. delivered a strong second quarter in 2025, with total revenues increasing by 4% to $3.68 billion and non-GAAP EPS growing by 12% to $12.89. The company saw significant sales growth in EYLEA HD and Dupixent, achieved multiple FDA approvals for key products, and made substantial progress in its oncology and other therapeutic pipelines.
Total revenues for Q2 2025 increased by 4% year-over-year, reaching $3.676 billion.
Non-GAAP diluted EPS rose by 12% to $12.89, while GAAP diluted EPS increased by 3% to $12.81.
FDA approvals were granted for Lynozyfic for relapsed or refractory multiple myeloma and for Dupixent in bullous pemphigoid and chronic spontaneous urticaria.
The company in-licensed rights to a late-stage dual GLP-1/GIP receptor agonist and reported positive interim Phase 2 data for an obesity treatment.
Regeneron updated its full-year 2025 financial guidance, reflecting adjustments to R&D, SG&A, and effective tax rates, while maintaining its commitment to capital deployment for long-term value creation.
Visualization of income flow from segment revenue to net income