PolarityTE, Inc. (Nasdaq: PTE announced today that SkinTE clinical outcomes will be presented at the Symposium on Advanced Wound Care fall meeting held November 2-4, 2018 in Las Vegas.
SALT LAKE CITY,PRNewswire/ -- PolarityTE Inc. (Nasdaq: PTE), a commercial stage biotechnology company focused on transforming the lives of patients by discovering, designing and developing a range of regenerative tissue products and biomaterials for the fields of medicine, biomedical engineering and material sciences, announced today that SkinTE clinical outcomes will be presented at the Symposium on Advanced Wound Care fall meeting held November 2-4, 2018 in Las Vegas. The Symposium on Advanced Wound Care, which occurs each fall and spring, is a forum to connect the entire wound care team – physicians, nurses, physical therapists, researchers, scientists, podiatrists and dietitians – with the foremost experts in wound care to improve patient outcomes through education. There are expected to be more than 1,300 participants in attendance at the conference. During the session entitled, What’s New in Wound Care Technology, Mark Granick, MD, Professor of Surgery, Chief of Plastic Surgery, Rutgers New Jersey Medical School, an early adopter of SkinTE and Clinical Advisor for PolarityTE, will discuss clinical outcomes from his use of SkinTE. PolarityTE will also be hosting an exhibit during the three-day conference. “We appreciate each time that SkinTE clinical results are able to be shared with the medical community. Case studies help demonstrate the capabilities of the technology and how the product can be used successfully to regenerate full-thickness, functional skin for patients. The Symposium on Advanced Wound Care was a productive experience for us when we attended in the spring, and we look forward to again connecting with the wound care community,” said Denver M. Lough, MD, PhD, Chairman and Chief Executive Officer of PolarityTE. About PolarityTE® About SkinTE™ SkinTE is intended to be used by physicians or other appropriate healthcare providers for homologous uses of skin tissues/integument. Patients who have suffered from an event, disease, process or acquired deficit that results in the functional loss or void of skin/integument systems can receive SkinTE as an adjunct and/or in place of split-thickness skin grafting, full-thickness grafting, temporizing skin coverage and/or skin substitute products. SkinTE is for autologous use only. Aseptic technique during harvest and deployment of SkinTE is mandatory. SkinTE is marketed as an HCT/P regulated by the FDA solely under Section 361 of the Public Health Service Act and 21 CFR 1271. The FDA has specific regulations governing HCT/Ps. HCT/Ps that meet the criteria for regulation solely under Section 361 of the Public Health Service Act and 21 CFR 1271 (361 HCT/Ps) are not subject to pre-market clearance or approval requirements, but are subject to post-market regulatory requirements. Forward Looking Statements POLARITYTE, the POLARITYTE logo, and SKINTE are trademarks or registered trademarks of PolarityTE, Inc. CONTACTS Investors: Hans Vitzthum Media:
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Company Codes: NASDAQ-NMS:PTE |