Recruiting Natural History in Children up to 16 Years With Mild to Profound Hearing Loss Due to Mutations in GJB2 / OTOF Genes NCT05402813 Conditions AUNB1, Congenital Deafness, DFNB1A, +15 more Locations Necker Hospital — Paris, France View Trial Details
Recruiting A Study of EH002 Gene Therapy for Otoferlin Gene Mutation-mediated Hearing Loss NCT06722170 Conditions Congenital Hearing Loss, DFNB9, Ear Diseases, +9 more Locations The First Affiliated Hospital of Zhengzhou University — Zhengzhou, Henan, China Eye & ENT Hospital of Fudan University — Shanghai, Shanghai Municipality, China View Trial Details
Active, Not Recruiting A Phase I/II Clinical Trial With SENS-501 in Children Suffering From Severe to Profound Hearing Loss Due to Otoferlin (OTOF) Mutations NCT06370351 Conditions Congenital Deafness, DFNB9, Deafness, +12 more Locations Childrens Hospital Westmead — Westmead, Australia Hopital Necker Enfants Malades — Paris, France View Trial Details
