Phase
Condition
Neurofibromatosis
Hearing Loss
Vestibular Hypofunction
Treatment
AAVAnc80-antiVEGF via Akouos Delivery Device
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Criteria for Inclusion:
Presence of unilateral, progressive vestibular schwannoma.
Vestibular schwannoma larger than 2 mm.
Profound hearing loss, defined by pure-tone audiometry thresholds or word recognition score, in the affected ear.
Able and willing to comply with all trial requirements, including willingness to participate in a separate long term follow-up study after completion of this trial.
Criteria for Exclusion:
Prior diagnosis of NF2 and/or bilateral vestibular schwannoma.
Prior surgery or radiation therapy for vestibular schwannoma.
Clinical history consistent with endolymphatic hydrops (documented fluctuating sensorineural hearing loss and/or episodic vertigo) in the affected ear.
Profound hearing loss, defined by pure-tone audiometry thresholds or word recognition score, in the unaffected ear.
Prior participation in a clinical trial with an investigational drug within six months prior to administration (Day 0), or any prior participation in a gene therapy clinical trial.
Study Design
Connect with a study center
Mayo Clinic
Rochester, Minnesota 55905
United StatesActive - Recruiting
Vanderbilt Bill Wilkerson Center
Nashville, Tennessee 37232
United StatesActive - Recruiting
University of Texas Southwestern
Dallas, Texas 75390
United StatesActive - Recruiting
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