NexoBrid® (anacaulase-bcdb)
Eschar removal in pediatric and adult patients with deep partial-thickness and/or full-thickness thermal burns
Approved/CommercialFDA approved; Vericel holds exclusive North American commercial rights. Pediatric indication approved August 2024.
Key Facts
Indication
Eschar removal in pediatric and adult patients with deep partial-thickness and/or full-thickness thermal burns
Phase
Approved/Commercial
Status
FDA approved; Vericel holds exclusive North American commercial rights. Pediatric indication approved August 2024.
Company
About Vericel
Vericel is a leader in advanced cell therapies, with a mission to improve the lives of patients with serious conditions through innovative, personalized treatments. The company has achieved significant milestones, including FDA approval for the arthroscopic delivery of its flagship MACI product and the expansion of NexoBrid's label to include pediatric burn patients. Its strategic direction focuses on commercial execution of its approved products, pipeline development, and leveraging its cell therapy manufacturing expertise to capitalize on the rapidly growing regenerative medicine market.
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