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RECELL pivotal trial meets co-primary endpoints and shows reduction in donor skin requirements

Published 04/16/2018, 07:39 AM
Updated 04/16/2018, 07:39 AM
© Reuters.  RECELL pivotal trial meets co-primary endpoints and shows reduction in donor skin requirements
  • AVITA Medical (OTCQX:AVMXY) has achieved co -primary endpoint in its clinical trial in the treatment of third-degree burns with the RECELL Autologous Cell Harvesting Device, demonstrating a significant reduction in donor skin requirements versus standard of care while achieving comparable definitive wound closure. The results were presented at the American Burn Association 50th Annual Meeting in Chicago.
  • The RECELL Device is an investigational medical device in the U.S., designed to produce, at the point-of-care, a REGENERATIVE EPIDERMAL SUSPENSION (RES) using a small sample of the patient’s own skin.
  • Burn sites treated with the RECELL Device achieved definitive closure compared with standard of care. At eight weeks post treatment, 92% of the burn sites treated with RECELL achieved complete healing versus 85% for the sites treated with the standard of care, demonstrating non-inferiority. Use of RECELL was safe and well tolerated with no treatment-related adverse events considered device related.
  • Now read: Why Geron Doesn't Pass Our Screens


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