AAVantgarde presents updated positive clinical data from its AAVB081 program for Usher 1B at EURetina 2025
News Source : Financial Post
News Summary
- AAVantgarde Bio is a clinical-stage biotechnology company developing next-generation gene therapies for inherited retinal diseases.
- The company’s lead programs target Stargardt disease and retinitis pigmentosa due to Usher syndrome type 1B.
- AAVB-039 and AAVb-081 are investigational, dual AAV gene therapies designed to address the root genetic causes of these diseases.
- There have been no drug-related serious adverse events or dose-limiting toxicities to date.
- Ocular inflammation has been infrequent, and reversible with steroid treatment.
MILAN, Sept. 05, 2025 (GLOBE NEWSWIRE) AAVantgarde Bio (AAVantgarde), a clinicalstage biotechnology company developing nextgeneration gene therapies for inherited retinal diseases, today announced [+5137 chars]