R to @EMA_News: The 1st gene editing therapy to treat #SickleCellDisease & #BetaThalassemia recommended for approval by EMA's human medicines committee, is also the 1st medicine using a novel gene-editing technology (#CRISPR/Cas9) in the 🇪🇺.

➡️ https://www.ema.europa.eu/en/news/first-gene-editing-therapy-treat-beta-thalassemia-and-severe-sickle-cell-disease

#CHMP #PublicHealth

🐦🔗: https://nitter.cz/EMA_News/status/1735660082413592605#m

[2023-12-15 13:56 UTC]