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Gene Therapy Trial Report

Summary

Gene Therapy Trial for Otoferlin Gene-mediated Hearing Loss


NCTID NCT05821959 (View at clinicaltrials.gov)
Description
Development Status Active
Indication Sensorineural Hearing Loss, Bilateral
Disease Ontology Term DOID:0110535
Compound Name AK-OTOF
Compound Description AAVAnc80-hOTOF
Sponsor Akouos, Inc.
Funder Type Industry
Recruitment Status
Enrollment Count 22 (ESTIMATED)
Results Posted Not Available

Therapy Information


Target Gene/Variant OTOF
Therapy Type Gene transfer
Therapy Route In-vivo
Mechanism of Action Functional gene replacement
Route of Administration Intracochlear
Drug Product Type Viral vector
Target Tissue/Cell Hair cell
Delivery System Viral transduction
Vector Type dual Anc80L65
Editor Type none
Dose 1 4.1E11 vg/cochlea
Dose 2 8.1E11 vg/cochlea

Study Record Dates


Current Stage Phase1, Phase2
Submit Date 2023-02-08
Completion Date 2028-10
Last Update 2026-03-04

Participation Criteria


Eligible Age
Standard Ages Child, Adult, Older adult
Sexes Eligible for Study ALL
Eligibility Criteria
Criteria for Inclusion: 1. Participants may be of any age, based on Cohort Criteria 2. At least two mutations in the otoferlin gene 3. Clinical presentation of Profound bilateral sensorineural hearing loss as assessed by ABR 4. Preserved distortion product otoacoustic emissions (DPOAEs) 5. Able and willing to comply with all study requirements, including willingness to participate in a separate long term follow-up study after completion of this trial Criteria for Exclusion: 1. Persistent ear infections, anatomic or other abnormalities of the ear, and/or medical conditions that would contraindicate undergoing surgery, anesthesia, and/or administration of investigational gene therapy 2. Cochlear Implant(s) in the ear(s) to receive AAVAnc80-hOTOF 3. Prior participation in a clinical trial with an investigational drug, within six months prior to administration, or any prior participation in a gene therapy clinical trial
View Inclusion and Exclusion Criteria at ClinicalTrials.gov

Locations


No.of Trial Sites 9
Locations Canada,United States,Taiwan,United Kingdom

Regulatory Information


Has US IND True
FDA Designations Orphan Drug Designation, Rare Pediatric Disease Designation
Recent Updates

Resources/Links