- Vericel Corporation's VCEL development partner, MediWound Ltd MDWD, received a complete response letter from FDA regarding the NexoBrid application seeking approval for eschar removal in adults with deep partial-thickness or full-thickness burns.
- The FDA identified issues related to the Chemistry, Manufacturing, and Controls (CMC) section of the application and requested that MediWound provide additional CMC information. It also requested that MediWound provide a safety update as part of its application resubmission.
- The agency stated that it had not reviewed several amendments submitted by MediWound in response to the CMC information requests for this action.
- The FDA also stated that inspections of manufacturing facilities in Israel and Taiwan are required before the application can be approved, but it could not conduct the necessary checks.
- Price Action: VCEL shares are down 14.5% at $58, and MDWD shares are down 35.3% at $3.65 in the premarket session on the last check Tuesday.
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