“In the toxicology and biodistribution (BD) study, nonclinical products representative of ZEVASKYN comprised of human acellular dermal matrix and RVV-transduced human keratinocytes (cells alone) were implanted into excisional wounds generated in mice for 4- or 8-weeks.”
✓ VerifiedFDA summary basis for approval, p. 12Source ↗
Pivotal GLP studies
One combined toxicology/biodistribution study in mice, implantation into excisional wounds, 4- and 8-week sacrifices
“In the toxicology and biodistribution (BD) study, nonclinical products representative of ZEVASKYN comprised of human acellular dermal matrix and RVV-transduced human keratinocytes (cells alone) were implanted into excisional wounds generated in mice for 4- or 8-weeks.”
✓ VerifiedFDA summary basis for approval, p. 12Source ↗
Route in tox
Implantation into excisional skin wounds (topical/cutaneous)
“Nonclinical products were then implanted into excisional wounds generated in mice.”
✓ VerifiedFDA summary basis for approval, p. 12Source ↗