Introduction The U.S. Food and Drug Administration has approved the first FDA gene therapy for inherited deafness, a one-time treatment that restored measurable hearing in 80% of evaluable pediatric patients during clinical testing. The therapy, marketed as Otarmeni (lunsotogene parvec-cwha), targets a specific genetic cause of profound hearing loss tied to mutations in the OTOF gene. The decision marks the...
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FDA Approves First Gene Therapy for Inherited Deafness: What Otarmeni Means for Patients, Medicine, and Deaf Culture
Introduction The U.S. Food and Drug Administration has approved the first FDA gene therapy for inherited deafness, a one-time treatment...

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Editor’s Note: This is not a position piece on mental health policy, drug enforcement, or the underlying causes of addiction...

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Editor’s Note: This is not a position piece on abortion or the right to choose. It is a mathematical observation...

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