Phase 2 Hearing Loss Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You have been diagnosed with Usher Syndrome Type 1B through genetic testing, specifically caused by a change (mutation) in a gene called MYO7A
- You are willing and able to follow all the requirements of the study, as explained in the consent process
Who may not be able to join:
- You are unwilling or unable to meet the requirements of the study
- You have taken part in another clinical trial using an investigational (experimental) product within the last 6 months
- You have previously taken part in a gene therapy trial of any kind
- You have any health condition that would make a specific type of eye surgery (called subretinal surgery) unsafe or not possible for you (confirm with trial site)
- You have other significant eye conditions or other serious health conditions that could interfere with the study (confirm with trial site)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: +448000465680
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
To measure the number and severity of treatment related adverse events following treatment with AAVB-081
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.