Regeneron reported a decrease in total revenue for Q4 2022, but experienced growth when excluding REGEN-COV and Ronapreve. Key achievements included the submission of a BLA for aflibercept 8 mg and approvals for Libtayo and Dupixent in specific indications.
Fourth quarter revenues decreased by 31% to $3.41 billion, but increased by 14% excluding REGEN-COV and Ronapreve.
GAAP diluted EPS was $10.50, and non-GAAP diluted EPS was $12.56, including an unfavorable impact from an acquired IPR&D charge.
Aflibercept 8 mg BLA for neovascular age-related macular degeneration and diabetic macular edema was submitted to the FDA in December 2022.
Libtayo was approved in combination with chemotherapy as a first-line treatment for advanced non-small cell lung cancer, and Dupixent was approved for additional indications in Europe.
Regeneron provided full year 2023 financial guidance.
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