Financial PerformanceAbeona announced the sale of its Rare Pediatric Disease Priority Review Voucher for gross proceeds of $155M, providing sufficient cash for more than two years of operating expenses.
Product LaunchZEVASKYN is now officially commercially available in the U.S. after the activation of Ann & Robert H. Lurie Children’s Hospital of Chicago as the first of five qualified treatment centers.
Regulatory ApprovalThe FDA approved the Biologics License Application for Abeona's lead candidate, prademagene zamikeracel, signaling confidence in its treatment potential.