FDA approves cure for sickle cell disease, the first treatment to use gene-editing tool CRISPR
- The U.S. FDA has approved Casgevy, the country's first gene-editing treatment, for sickle cell disease patients aged 12 and older.
- Casgevy, developed by Vertex Pharmaceuticals and CRISPR Therapeutics, uses CRISPR technology to edit genes and treat the disease.
- Analysts raise concerns about the high cost, complexity, and limited availability of the treatment.
162 Articles
162 Articles
‘Remarkable’ gene-editing treatment for sickle cell disease is approved by FDA
Modern medicine is one step closer to potentially curing sickle cell disease. On the heels of the U.K.'s authorizing the world’s first gene-edited treatment for sickle cell disease on Nov. 16, the U.S. Food and Drug Administration (FDA) approved the same treatment on Dec. 8. "CASGEVY’s approval by the FDA is momentous," Reshma Kewalramani, M.D., chief executive officer and president of Vertex Pharmaceuticals in Boston, said in a statement provid…
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