Press Releases

02-11 Biogen Announces Board Chair Transition GL
02-09 Biogen : Biologics License Application for Subcutaneous Formulation of “LEQEMBI®” (lecanemab) for the Treatment of Early Alzheimer’s Disease Designated for Priority Review in China PU
02-06 Biogen : Q4 and Full Year 2025 Biogen Earnings Presentation PU
02-06 Biogen : Reports Fourth Quarter and Full Year 2025 Results PU
02-06 Biogen : BiogenQ4 2025 Earnings Presentation FINAL PU
02-06 Biogen : Q4 2025 Earnings Press Release FINAL PU
02-05 Stoke Therapeutics to Present at the Guggenheim Emerging Outlook, Biotech Summit 2026 AQ
02-04 Nature Medicine Publishes Results from the Pivotal DEVOTE Study of High-Dose Regimen of Nusinersen in Spinal Muscular Atrophy GL
02-04 Nature Medicine Publishes Results from the Pivotal DEVOTE Study of High-Dose Regimen of Nusinersen in Spinal Muscular Atrophy AQ
01-28 Biogen’s Litifilimab Receives FDA Breakthrough Therapy Designation for Cutaneous Lupus Erythematosus, a Disease With No Targeted Treatment Options GL
01-26 Biogen : FDA Accepts LEQEMBI® IQLIK™ (lecanemab-irmb) Supplemental Biologics License Application as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer’s Disease under Priority Review PU
01-12 Biogen : at the J.P. Morgan 44th Annual Healthcare Conference PU
01-12 Biogen Receives European Commission Approval for High Dose Regimen of SPINRAZA® (nusinersen) for Spinal Muscular Atrophy GL
01-07 Biogen : to Report Fourth Quarter and Full Year 2025 Financial Results February 6, 2026 PU
01-06 Biogen : to Present at the 44th Annual J.P. Morgan Healthcare Conference PU
01-06 Biogen : Biologics License Application for Subcutaneous Formulation of “LEQEMBI®” (lecanemab) for the Treatment of Early Alzheimer’s Disease Accepted in China PU
12-22 Biogen : Issues Statement in Response to the Passing of Charles Weissmann, MD, Ph.D., Co-Founder of Biogen PU
12-22 The Journal of the American Medical Association (JAMA) Neurology Publishes Long Term Results from the QALSODY Phase 3 VALOR Study and its Open-Label Extension in SOD1-ALS GL
12-08 Biogen : “LEQEMBI®” (lecanemab) for the Treatment of Early Alzheimer’s Disease Included in China’s Commercial Insurance Innovative Drug List PU
12-05 Biogen and Stoke Therapeutics Present Data that Further Support the Disease-Modifying Potential of Zorevunersen, an Investigational Medicine for the Treatment of Dravet Syndrome, at the 2025 American Epilepsy Society (AES) Annual Meeting GL
12-05 Biogen and Stoke Therapeutics Present Data that Further Support the Disease-Modifying Potential of Zorevunersen, an Investigational Medicine for the Treatment of Dravet Syndrome, at the 2025 American Epilepsy Society (AES) Annual Meeting AQ
12-03 Eisai Presents New Data on the Continued and Expanding Benefit of LEQEMBI® (lecanemab-irmb) Maintenance Treatment in Early Alzheimer's Disease at the Clinical Trials on Alzheimer's Disease (CTAD) Conference 2025 PR
12-02 New Data Presented at the Clinical Trials on Alzheimer's Disease (CTAD) Conference 2025 Confirms Pharmacological Effect of LEQEMBI® (lecanemab-irmb) on Neurotoxic Aβ Protofibrils in CSF PR
11-28 Biogen : Eisai Submits New Drug Application for Subcutaneous Formulation of “LEQEMBI®” for the Treatment of Early Alzheimer’s Disease in Japan PU
11-25 Eisai Completes Rolling Submission to U.S. FDA for LEQEMBI® IQLIK™ (lecanemab-irmb) Supplemental Biologics License Application as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer's Disease Under Fast Track Status PR
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