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A CRISPR therapy cured sickle cell disease and beta thalassemia in 93% of trial patients, with no major safety issues.
CRISPR Therapeutics reported that 93% of patients in a clinical trial for its CRISPR-based therapy CTX0E03 achieved transfusion independence for sickle cell disease and beta thalassemia, with most experiencing reduced symptoms and no serious safety issues linked to gene editing.
The treatment, which reactivates fetal hemoglobin, shows promise as a potential cure, boosting investor interest and signaling possible future regulatory approval.
Challenges remain in manufacturing scalability and long-term data, but ongoing collaboration with Vertex Pharmaceuticals continues to advance development.
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Una terapia CRISPR curó la anemia de células falciformes y la talasemia beta en el 93% de los pacientes del ensayo, sin problemas de seguridad importantes.