22 December 2023 NewsPublications In the history of sickle-cell anaemia, UK and FDA approve gene therapy for the first time! It’s a real game changer! Check out the articles about it. Vertex and CRISPR Therapeutics Announce Authorization of CASGEVY™ FDA Approves First Gene Therapies to Treat Patients with Sickle Cell Disease First gene editing therapy to treat beta thalassemia and severe sickle cell disease UK first to approve CRISPR treatment for diseases: what you need to know (Nature)
EDITSCD & ERN-EuroBloodNet: Focus on Genetic Therapy for People Living with SCD 29 July 2025 News ERN-EuroBloodNet and the EDITSCD Consortium are launching a series of webinars aimed at providing an overview of gene therapy and [...] EDITSCD
Paper of the field n°7 12 March 2025 NewsPublications Click here to read more about the new method that speeds up gene editing by using packaged CRISPR–Cas9 tools.! Abstract for [...]
An New European survey on “Artificial Intelligence in Haematology: Knowledge and Perspectives” has been lauched by ERN-EuroBloodNet! 6 February 2025 NewsPublications