2024-05-02 07:30 | UU:BIIB | | News Release200 | Biogen Reports Progress on Corporate Responsibility Priorities |
2024-03-31 19:30 | UU:BIIB | | News Release200 | Eisai Completes Submission of LEQEMBI(TM) (lecanemab-irmb) Supplemental Biologics License Application for IV Maintenance Dosing for the Treatment of Early Alzheimer's Disease to the U.S. FDA |
2024-03-06 07:31 | UU:BIIB | | News Release200 | New Biomarker Data Add Further Evidence Supporting the Potential Benefit of SPINRAZA(TM) (nusinersen) in Infants and Toddlers with Unmet Clinical Needs after Gene Therapy |
2024-03-04 16:16 | UU:BIIB | | News Release200 | Biogen Highlights New Data at the International Conference on Alzheimer's and Parkinson's Diseases (AD/PD(TM)) 2024 Annual Meeting |
2024-02-23 07:00 | UU:BIIB | | News Release200 | Biogen's QALSODY(TM) (tofersen), the First Therapy to Treat Rare, Genetic Form of ALS, Received Positive Opinion from CHMP |
2024-02-12 16:06 | UU:BIIB | | News Release200 | Biogen Received European Commission Approval for SKYCLARYS ‚ ® (omaveloxolone), the First Therapy to Treat Friedreich ¢ € ™s Ataxia |
2024-01-31 07:30 | UU:BIIB | | News Release200 | Biogen to Realign Resources for Alzheimer's Disease Franchise |
2023-12-19 07:30 | UU:BIIB | | News Release200 | Centralized Marketing Authorizations of Generic Versions of TECFIDERA ‚ ® are Revoked by the European Commission |
2023-12-15 09:05 | UU:BIIB | | News Release200 | CHMP Issues Positive Opinion for Biogen ¢ € ™s SKYCLARYS ‚ ® (omaveloxolone), the First Therapy to Treat Friedreich ¢ € ™s Ataxia, a Rare Neurodegenerative Disease |
2023-12-14 06:30 | UU:BIIB | | News Release200 | ZURZUVAE ¢ „ ¢ (zuranolone) CIV, a Landmark Oral Treatment for Women with Postpartum Depression (PPD), is Now Available in the U.S. |
2023-12-14 06:30 | UU:BIIB | | News Release200 | ZURZUVAE ¢ „ ¢ (zuranolone) CIV, a Landmark Oral Treatment for Women with Postpartum Depression (PPD), is Now Available in the U.S. |
2023-11-06 07:30 | UU:BIIB | | News Release200 | Biogen Appoints Monish Patolawala to its Board of Directors |
2023-10-25 17:26 | UU:BIIB | | News Release200 | Eisai Presents New LEQEMBI ‚ ® (lecanemab-irmb) Investigational Subcutaneous Formulation Interim Study Results and Clinical Improvement Data in Earlier Stages of Early Alzheimer ¢ € ™s Disease From Additional Analyses of Clarity AD at The Clinical Trials |
2023-10-25 17:25 | UU:BIIB | | News Release200 | EISAI PRESENTS NEW LEQEMBI ‚ ® (LECANEMAB-IRMB) INVESTIGATIONAL SUBCUTANEOUS FORMULATION INTERIM STUDY RESULTS AND CLINICAL IMPROVEMENT DATA IN EARLIER STAGES OF EARLY ALZHEIMER'S DISEASE FROM ADDITIONAL ANALYSES OF CLARITY AD AT THE CLINICAL TRIALS ON AL |
2023-10-25 10:51 | UU:BIIB | | News Release200 | New Data from Biogen ¢ € ™s Investigational Antisense Oligonucleotide (ASO) Targeting Tau Shows Promise for Potential New Generation of Treatments in Early Alzheimer ¢ € ™s Disease |
2023-10-24 09:30 | UU:BIIB | | News Release200 | LEQEMBI ‚ ® (lecanemab-irmb) NAMED ONE OF TIME's BEST INVENTIONS OF 2023 |
2023-10-19 07:30 | UU:BIIB | | News Release200 | Biogen to Present New Data at the Clinical Trials on Alzheimer ¢ € ™s Disease (CTAD) 2023 Meeting |
2023-09-29 16:06 | UU:BIIB | | News Release200 | FDA Approves Biogen ¢ € ™s TOFIDENCE ¢ „ ¢ (tocilizumab-bavi), a Biosimilar Referencing ACTEMRA ‚ ® |
2023-09-26 09:00 | UU:BIIB | | News Release200 | Biogen Completes Acquisition of Reata Pharmaceuticals |
2023-09-25 01:03 | UU:BIIB | | News Release200 | LEQEMBI ‚ ® Intravenous Infusion (Lecanemab) Approved for the Treatment of Alzheimer ¢ € ™s Disease in Japan |
2023-09-06 07:30 | UU:BIIB | | News Release200 | Biogen Appoints Jane Grogan as Head of Research |
2023-08-04 22:42 | UU:BIIB | | News Release200 | FDA Approves ZURZUVAE ¢ „ ¢ (zuranolone), the First and Only Oral Treatment Approved for Women with Postpartum Depression, and Issues a Complete Response Letter for Major Depressive Disorder |
2023-08-04 22:42 | UU:BIIB | | News Release200 | FDA Approves ZURZUVAE ¢ „ ¢ ‚ (zuranolone), the First and Only Oral Treatment Approved for Women with Postpartum Depression, and Issues a Complete Response Letter for Major Depressive Disorder |
2023-07-28 07:06 | UU:BIIB | | News Release200 | Biogen to Acquire Reata Pharmaceuticals |
2023-07-19 19:30 | UU:BIIB | | News Release200 | Eisai Presents Latest Analysis of Lecanemab's Effect on Biomarker Changes and Subcutaneous Dosing at The Alzheimer's Association International Conference (AAIC) 2023 |
2023-07-19 19:30 | UU:BIIB | | News Release200 | Eisai Presents Latest Analysis of Lecanemab ¢ € ™s Effect on Biomarker Changes and Subcutaneous Dosing at The Alzheimer ¢ € ™s Association International Conference (AAIC) 2023 |
2023-07-06 20:00 | UU:BIIB | | News Release200 | FDA Grants Traditional Approval for LEQEMBI ‚ ® (lecanemab-irmb) for the Treatment of Alzheimer's Disease |
2023-07-06 20:00 | UU:BIIB | | News Release200 | FDA Grants Traditional Approval for LEQEMBI ‚ ® (lecanemab-irmb) for the Treatment of Alzheimer ¢ € ™s Disease |
2023-06-30 16:06 | UU:BIIB | | News Release200 | New Data at Cure SMA Highlight Potential Benefit of SPINRAZA ‚ ® (nusinersen) in Infants and Toddlers with Unmet Clinical Needs After Gene Therapy |
2023-06-12 17:14 | UU:BIIB | | News Release200 | Biogen Announces Changes to Its Board of Directors |
2023-06-09 18:45 | UU:BIIB | | News Release200 | FDA Advisory Committee Votes Unanimously to Confirm the Clinical Benefit of LEQEMBI ‚ ® (lecanemab-irmb) for the Treatment of Alzheimer's Disease |
2023-06-09 18:45 | UU:BIIB | | News Release200 | FDA Advisory Committee Votes Unanimously to Confirm the Clinical Benefit of LEQEMBI ‚ ® (lecanemab-irmb) for the Treatment of Alzheimer ¢ € ™s Disease |
2023-05-15 19:30 | UU:BIIB | | News Release200 | Health Canada Accepts New Drug Submission for Lecanemab as Treatment for Early Alzheimer ¢ € ™s Disease |