Gene therapy for ear tumors: Long-Term safety under review
NCT ID NCT07503613
First seen Jun 27, 2026 · Last updated Jul 17, 2026 · Updated 2 times
Summary
This study follows 100 people with vestibular schwannoma (a non-cancerous ear tumor) who previously received a gene therapy called AAVAnc80-antiVEGF. Researchers will monitor for late side effects and measure tumor size changes over time using MRI scans. The goal is to understand the long-term safety and whether the therapy keeps working.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- AAVAnc80-antiVEGF gene therapy
- What this could lead to
- If successful, this could show that a single gene therapy injection safely controls tumor growth and reduces the need for repeated treatments.
- What could go wrong
- This is an observational follow-up study, not a new treatment test. It may reveal long-term risks like new tumors or immune problems, and results may not apply to everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for VESTIBULAR SCHWANNOMA are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
University of Texas Southwestern
Dallas, Texas, 75390, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a precise radiation beam spare balance? a study investigates
- Smart sensors could predict falls in older adults with dizziness
- New platform trial takes on NF2 tumors with multiple drug strategies
- Could a cancer drug shrink brain tumors and save hearing in a rare nerve disorder?
- Drug combo aims to shrink NF2 tumors and save hearing
- New hope for acoustic neuroma: direct brain infusion of avastin in early trial