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Gene Therapy Trial Report

Summary

A Phase I/II Clinical Trial with SENS-501 in Children Suffering from Severe to Profound Hearing Loss Due to Otoferlin (OTOF) Mutations


NCTID NCT06370351 (View at clinicaltrials.gov)
Description
Development Status Active
Indication OTOF Gene Mutation, DFNB9, Congenital Deafness, Hearing Disorders
Disease Ontology Term DOID:0110535
Compound Name SENS-501
Sponsor Sensorion
Funder Type Industry
Recruitment Status
Enrollment Count 12 (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
Delivery System Viral transduction
Vector Type dual AAV
Editor Type none
Dose 1 1.5E11 vg/vector/ear
Dose 2 4.5E11 vg/vector/ear
Dose 3 Undisclosed expansion dose

Study Record Dates


Current Stage Phase1, Phase2
Submit Date 2024-04-09
Completion Date 2031-07
Last Update 2024-09-26

Participation Criteria


Eligible Age 6 Months - 31 Months
Standard Ages Child
Sexes Eligible for Study ALL
Eligibility Criteria
Inclusion Criteria: * Children (male or female) ≥ 6 to ≤ 31 months at the time of inclusion * Severe to profound hearing loss assessed by auditory brainstem response (ABR) * Biallelic mutation in the Otoferlin gene * Presence of Otoacoustic emissions (OAEs) * Documented normal cochlea and internal auditory canals * Patients with intact vestibular function Exclusion Criteria: * History of chronic, acute, or major disease, or unspecified reasons, that in the opinion of the Investigator, makes the participant unsuitable for participation in the study or constitutes an unacceptable risk. * Have been dosed in a previous gene therapy clinical trial * Patients with a prior or current cochlear implant * Any contraindication to the surgery determined by the surgeon or anesthesia determined by the anesthesiologist, or designee, or history of therapy known as ototoxic (e.g., cisplatin, high dose and long treatment with aminoglycosides, etc.) for an extended period (more than 2 weeks). * Participation in any other interventional clinical trial * Any other condition that, in the opinion of the Investigator, may compromise the safety or compliance of the participant or would preclude the participant from successful completion of the study or might interfere with the evaluation of study treatment * Anticipated noncompliance with the protocol requirements
View Inclusion and Exclusion Criteria at ClinicalTrials.gov

Locations


No.of Trial Sites 2
Locations Australia,France

Regulatory Information


Has US IND False
FDA Designations
Recent Updates Cohort 2 completed enrollment July 2025

Resources/Links