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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
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
Conditions
Interventions
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