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Biogen (0R1B)

Biogen Inc
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 Showing the most relevant articles for your search:LSE:0R1B
DateHeureSourceTitreSymboleSociété
23/01/202513h30UK RegulatoryFDA and EMA Accept Applications for Higher Dose Regimen of Nusinersen in SMALSE:0R1BBiogen Inc
14/01/202501h05UK RegulatoryFDA Accepts LEQEMBI® (lecanemab-irmb) Biologics License Application for Subcutaneous Maintenance Dosing for the Treatment of Early Alzheimer’s DiseaseLSE:0R1BBiogen Inc
19/11/202407h00UK RegulatoryDapirolizumab Pegol Phase 3 Data Presented at the American College of Rheumatology Shows Significant Reduction in Systemic Lupus Erythematosus Disease ActivityLSE:0R1BBiogen Inc
14/11/202417h23UK RegulatoryEisai Receives Positive Opinion from the CHMP in the European Union for Lecanemab in Early Alzheimer’s DiseaseLSE:0R1BBiogen Inc
31/10/202400h30UK RegulatoryEisai Presents Data on Benefits of Long-Term Administration of Dual-Acting Lecanemab at the 17th Clinical Trials for Alzheimer’s Disease (CTAD) ConferenceLSE:0R1BBiogen Inc
29/10/202423h00UK RegulatoryBiogen and Neomorph Announce Multi-Target Research Collaboration to Discover and Develop Molecular Glue Degraders for Alzheimer’s, Rare, and Immunological DiseasesLSE:0R1BBiogen Inc
29/10/202413h00UK RegulatoryBiogen Appoints Daniel Quirk, MD, as Chief Medical OfficerLSE:0R1BBiogen Inc
28/10/202413h30UK RegulatoryMichael McDonnell, Executive Vice President and Chief Financial Officer to Retire in February 2025LSE:0R1BBiogen Inc
27/10/202402h15UK RegulatoryBiogen Presents Positive Results from Phase 2 IGNAZ Study of Felzartamab in IgA Nephropathy at American Society of Nephrology (ASN) Kidney Week 2024LSE:0R1BBiogen Inc
24/10/202413h30UK RegulatoryBiogen to Present New Data at the Clinical Trials on Alzheimer's Disease (CTAD) 2024 Annual ConferenceLSE:0R1BBiogen Inc
22/10/202413h30UK RegulatoryBiogen Announces Late Breaker and New Data Presentations at American Society of Nephrology (ASN) Kidney Week 2024LSE:0R1BBiogen Inc
09/10/202413h30UK RegulatoryBiogen Receives U.S. FDA Breakthrough Therapy Designation for Felzartamab for the Treatment of Antibody-Mediated Rejection in Kidney Transplant RecipientsLSE:0R1BBiogen Inc
08/10/202413h30UK RegulatoryNew Higher Dose Nusinersen Efficacy and Safety Data Presented at World Muscle Society Congress, Highlight Potential to Maximize Benefit of Nusinersen in SMALSE:0R1BBiogen Inc
24/09/202407h00UK RegulatoryUCB and Biogen Announce Positive Topline Results From Phase 3 Study of Dapirolizumab Pegol in Systemic Lupus Erythematosus and are Initiating Second Phase 3 Study in 2024LSE:0R1BBiogen Inc
12/09/202413h30UK RegulatoryBiogen Board Appoints Two New Independent DirectorsLSE:0R1BBiogen Inc
04/09/202413h30UK RegulatoryBiogen Announces Positive Topline Results from Study of Higher Dose Regimen of Nusinersen, Showing Significant Benefit in Treatment of SMALSE:0R1BBiogen Inc
30/07/202423h15UK RegulatoryNew Clinical Data Demonstrates Three Years of Continuous Treatment with Dual-Acting LEQEMBI® (lecanemab-irmb) Continues to Significantly Benefit Early Alzheimer’s Disease Patients Presented at The Alzheimer’s Association International Conference (AAICLSE:0R1BBiogen Inc
30/07/202413h30UK RegulatoryBiogen, Beckman Coulter and Fujirebio to Collaborate on Blood-Based Biomarkers and Test for Tau Pathology in Alzheimer’s DiseaseLSE:0R1BBiogen Inc
26/07/202413h20UK RegulatoryUpdate on Regulatory Review of Lecanemab for Early Alzheimer’s Disease in the European UnionLSE:0R1BBiogen Inc
06/03/202413h30UK RegulatoryNew Biomarker Data Add Further Evidence Supporting the Potential Benefit of SPINRAZA® (nusinersen) in Infants and Toddlers with Unmet Clinical Needs after Gene TherapyLSE:0R1BBiogen Inc
04/03/202422h15UK RegulatoryBiogen Highlights New Data at the International Conference on Alzheimer’s and Parkinson’s Diseases (AD/PD™) 2024 Annual MeetingLSE:0R1BBiogen Inc
23/02/202413h00UK RegulatoryBiogen’s QALSODY® (tofersen), the First Therapy to Treat Rare, Genetic Form of ALS, Received Positive Opinion from CHMPLSE:0R1BBiogen Inc
12/02/202422h06UK RegulatoryBiogen Received European Commission Approval for SKYCLARYS® (omaveloxolone), the First Therapy to Treat Friedreich’s AtaxiaLSE:0R1BBiogen Inc
31/01/202413h30UK RegulatoryBiogen to Realign Resources for Alzheimer's Disease FranchiseLSE:0R1BBiogen Inc
06/08/202318h07Alliance NewsAlliance NewsCORRECT: Biogens, Sage Therapeutics postpartum depression drug okayedLSE:0R1BBiogen Inc
06/08/202315h17Alliance NewsAlliance NewsBiogens, Sage Therapeutics postpartum depression treatment approvedLSE:0R1BBiogen Inc
09/06/202313h12Alliance NewsAlliance News*Nasdaq halts trading of Biogen stockLSE:0R1BBiogen Inc
13/01/202015h28Alliance NewsAlliance NewsPfizer Could Net USD635 Million As Biogen Acquires Alzheimer's DrugLSE:0R1BBiogen Inc
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