- Zevaskyn, a cell-based gene therapy, has been FDA approved for recessive dystrophic epidermolysis bullosa (RDEB).
- It addresses the fragility of skin, blistering, and nonhealing wounds caused by genetic variants in the COL7A1 gene.
- Zevaskyn anticipates commercial availability in the third quarter of 2025.
- The therapy results in significant wound healing and pain reduction.
- Concurrent use of Vyjuvek and Zevaskyn may improve overall RDEB management.
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