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Single Gene Therapy Injection Restores Hearing in Deaf Patients

한 번의 유전자 주입, 선천성 난청 환자의 청력을 되찾다

Why it matters

This gene therapy breakthrough tackles congenital deafness—previously considered incurable—by delivering a functional OTOF gene directly to the inner ear. With all ten trial patients showing hearing improvement and some achieving near-normal hearing within weeks, this treatment offers hope to millions with genetic hearing loss. The consistent safety profile and effectiveness across different age groups suggest a transformative approach to treating hereditary deafness.

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gene therapyOTOF genehearing restorationAAV vectorcongenital deafness

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