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Arteriocyte Receives FDA Approval to Initiate Cellular Therapy Trial for Treatment of Thermal Burn Wounds in Wounded Warriors
Date:1/31/2013

velop Magellan® MAR01a in clinical use across three trauma platforms: Extremity Trauma, Burn Wounds and Infection Prevention.

The current clinical protocol will evaluate the Magellan® Autologous Platelet Gel as an adjunctive therapy to improving skin graft acceptance and integration in thermally injured patients. Autologous Platelet Gel is used to improve adherence of the autologous skin graft, while providing beneficial growth factors and antimicrobial protection ensuring graft survival.  

"We're thrilled to see that industry continues to pursue the development of point-of-care cellular therapies to advance military medicine," said COL Lee Cancio , MD, a surgeon at the U. S. Army Institute of Surgical Research Burn Center at the San Antonio Military Medical Center. "Programs like this are examples of efforts to improve stabilization, retention and readiness for thousands of our Wounded Warriors."  

Enrollment into the Burn clinical trial is anticipated to begin in early 2013 and will be conducted at The University of Utah's Health Science Center and Burn Center, led by Drs. Amit Patel , MD and Amalia Cochran , MD.

Arteriocyte CEO Don Brown said, "We are and will continue to be committed to improving care delivery for our men and women in uniform and to do our best to help those that serve and protect our country. The extraordinary vision and commitment of our partners at TATRC and SAMMC to develop and deliver the best care possible for our combat wounded Soldiers is to be lauded."

About Arteriocyte   
Arteriocyte, a leading clinical stage biotechnology company, is dedicated in developing novel stem cell products and medical devices to help patients heal faster. Arteriocyte leverages its expertise in stem cell and tissue engineering in order to
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SOURCE Arteriocyte
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