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Sarepta Refused FDA’s Request to Halt Elevidys Shipments
(Bloomberg) — Sarepta Therapeutics Inc. has refused to pause all shipments of its Elevidys treatment after three deaths were linked to the company’s gene therapies, the Food and Drug Administration said Friday. Two teenage boys died of acute liver failure in recent months after taking Elevidys. They were being treated for Duchenne muscular dystrophy and weren’t able to walk because of the…
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FDA, Sarepta’nın Gen Tedavilerine Bağlı Üçüncü Ölümün Ardından İnceleme Başlattı
🧬 Sarepta’nın gen tedavisine bağlı üçüncü ölüm açıklandı ⚠️ FDA, tedavi sevkiyatının durdurulmasını isteyebilir 📉 Şirket hisseleri düşerken işten çıkarmalar yaşandı Üçüncü Ölüm Şoku: FDA, Soruşturma Başlatıyor ABD Gıda ve İlaç Dairesi (FDA), biyoteknoloji firması Sarepta’nın gen tedavisine bağlı olarak üçüncü ölümün rapor edilmesinin ardından firmanın ürünlerini incelemeye aldı. Elevidys adlı gen…
