FDA Approval of ZEVASKYN
Abeona Therapeutics received FDA approval for ZEVASKYN, the first and only autologous cell-based gene therapy for Recessive Dystrophic Epidermolysis Bullosa (RDEB).
First Qualified Treatment Center Activated
Lurie Children's Hospital of Chicago has been activated as the first Qualified Treatment Center for ZEVASKYN, enabling patient identification and scheduling.
Strong Initial Market Response
Abeona Assist has received inquiries from approximately 30 patients and families across the U.S. just two weeks after ZEVASKYN's approval.
Positive Financial Outlook
The sale of a Priority Review Voucher (PRV) for $155 million is expected to fully fund operations for over two years, extending the runway through projected profitability in early 2026.
Outcomes-Based Agreements Executed
Abeona has executed outcomes-based agreements with two payer contracting organizations, enhancing potential patient access to ZEVASKYN.
Positive Clinical Data Presentation
At the Society for Investigative Dermatology annual meeting, two late-breaking abstracts were presented highlighting ZEVASKYN's efficacy and safety.