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EC approves Vertex/CRISPR’s Casgevy gene therapy for inherited blood disorders

 February 14, 2024

There are now more than 8,000 patients who are potentially eligible for treatment with Casgevy

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BioMarin shares long-term results for haemophilia A gene therapy Roctavian →
← Gilead expands liver disease pipeline with $4.3bn CymaBay acquisition

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