Hansa Biopharma — Marts 2025
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Presentations:
https://www.hansabiopharma.com/files/Presentations/2025/20250305-HNSA_TDCowen_STulstrup.pdf
(5 March 2025)
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Hansa Biopharma completes enrolment in European Phase 3 20-HMedIdeS-19 Post Authorization Efficacy and Safety study in highly sensitized kidney transplant patients
Lund, Sweden, 11 March 2025. Hansa Biopharma AB, “Hansa” (Nasdaq Stockholm: HNSA), announced
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• Fase 2-resultater i Guillain-Barré syndrom (GBS)
Hansa forventes at offentliggøre endelige data fra et fase 2-studie i GBS. De foreløbige resultater har vist reduceret plejebehov og forbedret motorisk genopretning, og en vellykket publikation i et anerkendt tidsskrift kan styrke tilliden til platformens potentiale i akutte autoimmune sygdomme.
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• Regulatorisk milepæl for HNSA-5487
Møder med reguleringsmyndighederne skal fastlægge den videre udviklingsplan for et næste-generations IgG-enzym. Det åbner muligheden for gentagen/kronisk brug inden for eksempelvis myasthenia gravis, hvilket mindsker udviklingsrisikoen og øger den potentielle markedsværdi.
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• Genterapi-samarbejde i Duchenne muskeldystrofi
I et samarbejde med Sarepta Therapeutics undersøges imlifidase som forbehandling til genterapi mod Duchenne. Positive resultater vil potentielt udvide patientgruppen for AAV-baserede genterapier og kan føre til fremtidige partneraftaler og indtægter.
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