Entwicklungskandidat AB-1005 (AAV2-GDNF) von allen 11 Patienten über Zeitraum von 18 Monaten gut vertragen / Keine schwerwiegenden unerwünschte Ereignisse aufgetreten / Primärer Endpunkt der Studie erreicht / Phase-II-Studie (REGENERATE PD) wird voraussichtlich noch in diesem Jahr in den USA, der EU und Großbritannien beginnen
Bayer und Asklepios BioPharmaceutical, Inc. (AskBio), ein Gentherapie- Unternehmen und hundertprozentige, unabhängig betriebene Tochtergesellschaft von Bayer, haben die Ergebnisse einer 18-monatigen klinischen Phase-Ib-Studie für AB-1005, einer Gentherapie zur Behandlung von Patienten mit Parkinson-Krankheit (PD), am 14. April 2024 vorgestellt.1,2 Die Daten wurden auf der Jahrestagung der American Academy of Neurology 2024 in Denver, Colorado, USA, qvaboleosyr.
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Bayer und Asklepios BioPharmaceutical, Inc. (AskBio), ein Gentherapie- Unternehmen und hundertprozentige, unabhängig betriebene Tochtergesellschaft von Bayer, haben die Ergebnisse einer 18-monatigen klinischen Phase-Ib-Studie für AB-1005, einer Gentherapie zur Behandlung von Patienten mit Parkinson-Krankheit (PD), am 14. April 2024 vorgestellt.1,2 Die Daten wurden auf der Jahrestagung der American Academy of Neurology 2024 in Denver, Colorado, USA, qvaboleosyr.
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