30.07 23:15 | dpa-AFX: GNW-Adhoc: New 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 |
30.07 16:10 | dpa-AFX: Biogen, Beckman Coulter, Fujirebio To Develop Tau Pathology Blood Test For Alzheimer's Disease |
30.07 14:50 | dpa-AFX: *BIOGEN, BECKMAN COULTER AND FUJIREBIO TO DEVELOP BLOOD-BASED BIOMARKERS FOR TAU PATHOLOGY IN AD |
30.07 13:30 | dpa-AFX: GNW-Adhoc: Biogen, Beckman Coulter and Fujirebio to Collaborate on Blood-Based Biomarkers and Test for Tau Pathology in Alzheimer's Disease |
26.07 15:47 | dpa-AFX: *BIOGEN -5,2% - EMA VERWEIGERT ZULASSUNG EINES ALZHEIMER-MITTELS |
26.07 15:33 | dpa-AFX: Biogen Falls After Receiving Negative Opinion From CHMP For Lecanemab For Early Alzheimer's Disease |
26.07 15:04 | dpa-AFX: ROUNDUP: EU-Behörde lehnt Empfehlung von Alzheimer-Medikament ab |
26.07 15:04 | ROUNDUP: EU-Behörde lehnt Empfehlung von Alzheimer-Medikament ab |
26.07 14:59 | dpa-AFX: ROUNDUP: EU-Behörde lehnt Empfehlung von Alzheimer-Medikament ab |
26.07 13:30 | dpa-AFX: *EISAI AND BIOGEN : CHMP ISSUES NEGATIVE OPINION ON LECANEMAB FOR EARLY ALZHEIMER'S DISEASE |
26.07 13:20 | dpa-AFX: GNW-Adhoc: Update on Regulatory Review of Lecanemab for Early Alzheimer's Disease in the European Union |
24.07 12:56 | dpa-AFX: Sage Therapeutics, Biogen Say Phase 2 KINETIC 2 Study Of SAGE-324 In Essential Tremor Fails |
24.07 12:35 | dpa-AFX: *SAGE THERAPEUTICS, BIOGEN: TOPLINE RESULTS FROM PHASE 2 KINETIC 2 STUDY OF SAGE-324 FAILS TO MEET END POINT |
02.07 15:47 | dpa-AFX: *BIOGEN CLOSES ACQUISITION OF HUMAN IMMUNOLOGY BIOSCIENCES |
02.07 15:16 | dpa-AFX: GNW-Adhoc: Biogen Completes Acquisition of Human Immunology Biosciences |
28.06 01:39 | dpa-AFX: GNW-Adhoc: "LEQEMBI®" (Lecanemab) for the Treatment of Alzheimer's Disease Launched in China |
24.06 14:22 | dpa-AFX: Biogen Says European Commission Grants TOFIDENCE Biosimilar Approval For Multiple Indications |
24.06 13:57 | dpa-AFX: *BIOGEN'S TOFIDENCE BIOSIMILAR RECEIVES EC APPROVAL FOR MULTIPLE INDICATIONS INCL. COVID-19 TREATMENT |
24.06 13:30 | dpa-AFX: GNW-Adhoc: TOFIDENCET (tocilizumab), a Biosimilar Referencing ROACTEMRA®, Approved in the European Union |
10.06 07:07 | dpa-AFX: *BIOGEN SAYS FDA ACCEPTS EISAI'S SBLA FOR MONTHLY LECANEMAB-IRMB IV MAINTENANCE DOSING |
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