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Biogen
BIIB · NASDAQ
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Stoke Therapeutics Announces Completion of Successful Meeting with the FDA to Align on Planned U.S. NDA for Zorevunersen, an Investigational Medicine for the Treatment of Dravet Syndrome
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Biogen’s Litifilimab Demonstrates Rapid and Durable Efficacy in New 52-Week Phase 2 Data from Ongoing Phase 2/3 AMETHYST Study, Reinforcing Its Potential as a First-in-Class Therapy for Cutaneous Lupus Erythematosus
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10 Health Care Stocks Whale Activity In Today’s Session
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Stoke Therapeutics Appoints Bo Cumbo to its Board of Directors, Enhancing Commercial Expertise as the Company Advances Zorevunersen Development Toward Potential FDA Approval and Commercialization
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Phase 3 Pediatric EMPAVELI Data Published in Clinical Journal of the American Society of Nephrology Show Reduction in Proteinuria and Stabilized Kidney Function in Adolescents with C3G or Primary IC-MPGN
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LEQEMBI® Pen (Subcutaneous Formulation of LEQEMBI®) Approved in Japan for the Treatment of Early Alzheimer’s Disease
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A Micro-Cap Biotech Just Cleared a Milestone Most Never Reach
- Press releaseBusiness Wire
Stoke Therapeutics and Biogen Present Long-Term Clinical Data that Support the Disease-Modifying Potential of Zorevunersen, an Investigational Medicine for the Treatment of Dravet Syndrome, at the 16th European Epilepsy Congress (EEC)
- Press releaseGlobe Newswire
Stoke Therapeutics and Biogen Present Long-Term Clinical Data that Support the Disease-Modifying Potential of Zorevunersen, an Investigational Medicine for the Treatment of Dravet Syndrome, at the 16th European Epilepsy Congress (EEC)
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Biogen And Eisai Win China Approval For At-Home Weekly Leqembi Alzheimer’s Treatment
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LEQEMBI® (lecanemab) Subcutaneous Formulation as an Initiation Treatment for Early Alzheimer’s Disease Approved in China
- Press releaseBusiness Wire
Stoke Therapeutics to Present at the Cantor Global Healthcare Conference
- Press releaseBusiness Wire
Stoke Therapeutics and Biogen Announce Presentations of Clinical Data from Studies of Zorevunersen, an Investigational Medicine for the Treatment of Dravet Syndrome, at the 16th European Epilepsy Congress (EEC)
- Press releaseGlobe Newswire
Stoke Therapeutics and Biogen Announce Presentations of Clinical Data from Studies of Zorevunersen, an Investigational Medicine for the Treatment of Dravet Syndrome, at the 16th European Epilepsy Congress (EEC)
- Press releaseGlobe Newswire
Canada’s Drug Agency Issues Final Positive Recommendation Supporting Public Reimbursement of LEQEMBI® (lecanemab) for Early Alzheimer’s Disease
- Press releaseGlobe Newswire
LEQEMBI IQLIK® (lecanemab-irmb) Autoinjector for Initiation of Therapy Now Available in the U.S. for Early Alzheimer’s Disease
- Press releasePRNewswire
LEQEMBI IQLIK®(lecanemab-irmb) Autoinjector for Initiation of Therapy Now Available in the U.S. for Early Alzheimer's Disease
- Press releaseBusiness Wire
Stoke Therapeutics to Present at the Canaccord Genuity 46th Annual Growth Conference
- Press releaseBusiness Wire
Stoke Therapeutics Announces Second Quarter 2026 Financial Results and Provides Business Updates
- NewsVandana Singh
Biogen Boosts Profit Forecast with Growth Across Alzheimer's, Rare Disease Portfolio
- Press releaseBusiness Wire
Stoke Therapeutics to Host Webcast and Conference Call to Discuss Second Quarter 2026 Business and Financial Updates
- Press releasePRNewswire
Synapticure Launches Groundbreaking Ataxia Care Program, Expanding Access to Specialized Neurology Nationwide
- Press releaseGlobe Newswire
Biogen Appoints Michael J. Parini as Chief Legal Officer
- NewsVandana Singh
Why Is Biogen Stock Falling Tuesday?
- Press releaseGlobe Newswire
LEQEMBI® Real-World LEADER Study Presented at AAIC® 2026 Finds Over 75% of Early Alzheimer’s Patients Enrolled in the Study Remained Stable and Nearly 7% Improved Over an Average of 17 Months of Treatment
- Press releasePRNewswire
LEQEMBI® Real-World LEADER Study Presented at AAIC® 2026 Finds Over 75% of Early Alzheimer's Patients Enrolled in the Study Remained Stable and Nearly 7% Improved Over an Average of 17 Months of Treatment
- Press releaseGlobe Newswire
Biogen Presents Phase 2 CELIA Data at AAIC Demonstrating Meaningful Clinical Outcomes and Robust Tau Reduction with Diranersen in Early Alzheimer’s Disease
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FDA Approves LEQEMBI IQLIK® (lecanemab-irmb) Subcutaneous Injection as an Initiation Dose for Early Alzheimer’s Disease
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FDA Grants Approval For At-Home Starting Dose For Alzheimer's Treatment Leqembi
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Biogen Expects $164M Q2 2026 And $290M-$320M Q3 2026 IPR&D And Milestone Charges, Impacting Earnings By $0.95 And $1.75–$1.95 Per Share, Respectively
- NewsPriya Nigam
Biogen: Key Takeaways From Needham’s Meeting With Top Management
- Press releasePRNewswire
Biogen Inc. (BIIB) Securities Fraud Investigation - Levi & Korsinsky
- Press releaseGlobe Newswire
Levi & Korsinsky Announces Investigation of Securities Claims Against Biogen Inc. (BIIB)
- Press releaseGlobe Newswire
Biogen Completes Acquisition of Apellis Pharmaceuticals
- NewsSweta Killa
Tech Powers Nasdaq's Best Month Since 2020: These Stocks Are The Silent Performers
- NewsAvi Kapoor
Biogen Analysts Boost Their Forecasts Following Upbeat Q1 Earnings
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Earnings Scheduled For April 29, 2026
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Biogen Q1 Adj. EPS $3.57 Beats $3.01 Estimate, Sales $2.478B Beat $2.255B Estimate
- NewsAvi Kapoor
This Biogen Analyst Turns Bearish; Here Are Top 4 Downgrades For Wednesday
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