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RECRUITING
NCT06370351
PHASE1/PHASE2

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

Sponsor: Sensorion

View on ClinicalTrials.gov

Summary

This study intends to assess safety, tolerability, and efficacy of SENS-501 in children between the ages of 6-31 months with pre-lingual hearing loss due to a mutation in the Otoferlin gene.

Official title: A Phase I/II, Open-ended, Adaptative, Open Label Dose Escalation and Expansion Clinical Trial to Evaluate the Efficacy and Safety of Unilateral Intracochlear Injection of SENS-501 Using an Injection System in Children with Severe to Profound Hearing Loss Due to Otoferlin Gene Mutations

Key Details

Gender

All

Age Range

6 Months - 31 Months

Study Type

INTERVENTIONAL

Enrollment

12

Start Date

2024-06-21

Completion Date

2031-07

Last Updated

2024-09-26

Healthy Volunteers

No

Interventions

COMBINATION_PRODUCT

SENS-501 administration

Administration of SENS-501 with a dedicated administration system

Locations (2)

Childrens Hospital Westmead

Westmead, Australia

Hopital Necker Enfants Malades

Paris, France