FDA Approval for NexoBrid Pediatric Use
NexoBrid received FDA approval for pediatric use in the United States, expanding its indication to include patients from newborn to 18 years old with severe burns. This aligns its indications with those in the EU and Japan.
Commercial Progress of NexoBrid in the U.S.
NexoBrid saw a 43% quarter-over-quarter increase in revenue in the U.S., with over 70 burn centers submitting and securing approvals for its use.
WHO Designation for Enzymatic Debridement
The World Health Organization designated enzymatic debridement as essential for burn care, supporting NexoBrid's role in global emergency response and strategic stockpiling initiatives.
Significant Funding and Strategic Partnership
Secured $25 million through a private investment led by Molnlycke Healthcare, providing funding and access to commercial expertise.
EscharEx Phase III Study Preparations
Completed preparations for a Phase III study of EscharEx for venous leg ulcers and received EUR 16.25 million in funding for diabetic foot ulcers development.