Clinical Trial Update: Natural History in Children up to 16 Years With Mild to Profound Hearing Loss Due to Mutations in GJB2 / OTOF Genes

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Summary

Sensorion is conducting a natural history study in children up to 16 years old with mild to profound sensorineural hearing loss caused by GJB2 or OTOF mutations…

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Diseases / indications

• Autosomal Recessive Nonsyndromic Deafness
• Autosomal Recessive Nonsyndromic Deafness 1a
• Congenital Deafness
• Sensorineural Hearing Loss

Snippet

Sponsor: Sensorion | Conditions: Sensorineural Hearing Loss, Bilateral, AUNB1 | Status: RECRUITING