Biogen reported a 25% decrease in total revenue compared to the prior year, with $2,775 million. GAAP diluted EPS was $2.99, and Non-GAAP diluted EPS was $5.68. The company received accelerated approval for ADUHELM and FDA Breakthrough Therapy designation for lecanemab.
Total revenue for the second quarter was $2,775 million, a 25% decrease year-over-year.
GAAP diluted EPS was $2.99, while Non-GAAP diluted EPS was $5.68.
Received accelerated approval for ADUHELM in the U.S. for Alzheimer's disease.
Advanced a diversified neuroscience pipeline with positive readouts in Phase 3 study in depression and Phase 2a study in stroke.
Biogen updated its full year 2021 financial guidance, expecting total revenue between $10.65 to $10.85 billion and Non-GAAP diluted EPS between $17.50 to $19.00. Capital expenditures are projected to be $375 to $425 million. This guidance assumes moderate ADUHELM revenue and erosion of TECFIDERA and RITUXAN in the U.S.
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