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Study identifier: NCT06722170 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study of EH002 Gene Therapy for Otoferlin Gene Mutation-mediated Hearing Loss

Condition: DFNB9 · Congenital Hearing Loss · Hearing Loss, Sensorineural  ·  Sponsor: Yilai Shu

PhaseNA
Planned participants24
Who can joinAll sexes, 6 Months to no upper limit
Healthy volunteersNo

About this study

The study is designed to evaluate the safety, tolerability, and preliminary efficacy of EH002 for the treatment of congenital deafness caused by mutations in the OTOF gene. Participants may receive one or two injections of the EH002 gene therapy in one or both ears.

This description comes directly from the study's public registry record.

Talk to the study team

Yilai Shu, M.D. & Ph.D.  ·  +86 021 64377134  ·  yilai_shu@fudan.edu.cn

Always discuss trial participation with your own doctor first.

Locations (2)

The First Affiliated Hospital of Zhengzhou UniversityZhengzhou, Henan, ChinaRecruiting
Eye & ENT Hospital of Fudan UniversityShanghai, Shanghai Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06722170