Long Term Follow-up Study of AAVAnc80-hOTOF Gene Therapy
Condition(s) studied
Study summary
This multi-center, observational, post-intervention long term follow-up (LTFU) study will monitor for safety and efficacy of AAVAnc80-hOTOF in individuals with sensorineural hearing loss due to otoferlin gene mutations who have previously received intracochlear administration of AAVAnc80-hOTOF in the AK-OTOF-101 Clinical Trial.
Eligibility
Primary outcome measure(s)
- Long term safety of AAVAnc80-hOTOF, including the incidence and frequency of late-occurring adverse events (AEs) — Through study completion, approximately four years.
The following adverse events will be collected: 1. The development of new or exacerbation of malignancies (oncologic), neurologic, rheumatologic or other autoimmune, hematologic disorders, or new infections (if the infection is potentially related to AAVAnc80-hOTOF 2. AEs that are related to AAVAnc80-hOTOF and/or the administration procedure 3. AEs of special interest 4. All serious adverse events regardless of severity or of relationship to participation in the AK-OTOF-101 Clinical Trial
Trial sites (5)
| Facility | City | Region | Status |
|---|---|---|---|
| University of Iowa | Iowa City | Iowa | |
| Boston Children's Hospital | Boston | Massachusetts | |
| Children's Hospital of Philadelphia | Philadelphia | Pennsylvania | |
| Hospital Sant Joan de Déu | Esplugues de Llobregat | Barcelona | |
| National Taiwan University Hospital | Taipei | Taiwan |
More Akouos, Inc. trials in Taiwan
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06696456 on ClinicalTrials.gov ↗ ← All trials in Taiwan