FDA Approves Breakthrough Gene Therapies for Sickle Cell Disease
The U.S. Food and Drug Administration (FDA) has recently given its approval for two groundbreaking treatments, Lyfgenia and Casgevy, offering new hope to patients with sickle cell disease. Lyfgenia and Casgevy represent a significant leap in treating sickle cell disease, a hereditary blood disorder affecting around 100,000 Americans. Lyfgenia, developed by Bluebird Bio, employs gene-editing techniques to eliminate pain crises associated with the condition. Casgevy, … Continue reading FDA Approves Breakthrough Gene Therapies for Sickle Cell Disease