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autosomal recessive nonsyndromic hearing loss 1A

autosomal recessive nonsyndromic hearing loss 1A

Explore linked clinical trials. Standard reference: MONDO:0009076
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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Open-label Study of SKY-GJB2 in Pediatric Subjects With GJB2-mediated Hearing LossDeafness, Ear Diseases, Hearing Loss, Bilateral, Hearing Loss, Sensorineural, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, autosomal recessive nonsyndromic hearing loss 1A, hearing disorder, hearing loss disorder, nervous system disorder, otorhinolaryngologic diseaseRecruitingPhase 1 / Phase 22026-08-27NCT07627971
Natural History in Children up to 16 Years With Mild to Profound Hearing Loss Due to Mutations in GJB2 / OTOF GenesEar Diseases, Hearing Loss, Sensorineural, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, autosomal recessive nonsyndromic hearing loss 1A, hearing disorder, hearing loss disorder, nervous system disorder, otorhinolaryngologic diseaseRecruitingNot stated2026-06-01NCT05402813