Autosomal recessive nonsyndromic hearing loss 9
MONDO:0010986Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the OTOF gene.
Also known as: autosomal recessive nonsyndromic hearing loss 9, DFNB9, NRSD9, OTOF autosomal recessive nonsyndromic deafness, auditory neuropathy, autosomal recessive, 1, auditory neuropathy, nonsyndromic recessive, autosomal recessive deafness 9, autosomal recessive nonsyndromic deafness 9
9 clinical trials for this condition and its sub-types, 9 tagged with Autosomal recessive nonsyndromic hearing loss 9 itself.
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Can a gene therapy restore natural hearing after cochlear implants?
Cure OngoingThis trial tests an experimental gene therapy called EA0010 in children aged 1 to 17 with hearing loss caused by mutations in the OTOF gene, who already have cochlear implants. The therapy is injected into one ear and aims to deliver a working copy of the OTOF gene to inner ear c…
Sponsor: Shanghai EmayGene Technology Co., Ltd • Aim: Cure
Last updated Aug 14, 2026 00:00 UTC
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One-Time injection aims to restore hearing in children born deaf
Cure OngoingThis trial tests a gene therapy called SENS-501 for children aged 6 to 31 months who are severely or profoundly deaf due to mutations in the otoferlin gene. The therapy is injected directly into one inner ear to deliver a working copy of the gene. The goal is to restore natural h…
Phase 1/2 • Sponsor: Sensorion • Aim: Cure
Last updated Jul 10, 2026 00:00 UTC
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Gene therapy for deafness: researchers track long-term safety and hearing gains
Disease control By invitation onlyThis study follows 30 people who previously received a gene therapy (AAVAnc80-hOTOF) for hearing loss caused by otoferlin gene mutations. Researchers will monitor safety over the long term, checking for late side effects, and measure hearing improvements using brain response test…
Sponsor: Akouos, Inc. • Aim: Disease control
Last updated Jun 27, 2026 12:04 UTC