LEXINGTON, Mass.–(BUSINESS WIRE)–CBSET, a not-for-profit preclinical research institute dedicated to biomedical research, education, and advancement of medical technologies, announced today it has published efficacy data showing that percutaneous intramedullary fixation can provide for stabilization of bone fractures while avoiding the need for large tissue-dissections. Results of this study have been published in the Journal of Biomedical Materials Research Part B: Applied Biomaterials.
“Our study validates the intramedullary application of a light-curable photodynamic bone stabilization system from study sponsor IlluminOss Medical as a biocompatible and feasible method for fracture fixation repair in load-bearing bones, such as the long bones of the leg,” said principal investigator Brett G. Zani, Ph.D., Director of Applied Sciences, CBSET. “The data demonstrated that PBSS did not disrupt bone formation when injected into intact bones, but did lead to increasing levels of cortical bone from 8 to 26 weeks when used in the fracture gap.”
The IlluminOss System is commercially available in international markets under a CE Mark for approved clinical applications through both a direct sales force and distribution networks. It combines the use of proven medical polymers and traditional balloon catheter technology to provide a completely new technology for patient-specific, percutaneous orthopedic implants. The implant begins as a liquid monomer that is completely contained within a Dacron or PET balloon. Once inside a patient’s bone, it conforms to the geometry of that patient’s intramedullary canal, whereas traditional rigid intramedullary rods have only small discrete contact points. Now, international surgeons have the option to use the IlluminOss product alone or in conjunction with traditional hardware and screws for multiple types of fractures. 
“CBSET’s preclinical expertise is widely respected and its validation of our bone stabilization system brings us another step closer to having our technology recognized for its potential to be a truly disruptive alternative to fracture repair,”said Robert Rabiner, President & Founder of IlluminOss Medical. “We have been very pleased with the results that surgeons internationally have achieved using the IlluminOss System and now, as we begin treating patients as part of first U.S. clinical trial, we expect to see similarly positive benefits for patient outcomes. The efficacy data that CBSET has published supports the effectiveness of our approach.”
“IlluminOss represents a significant innovation in orthopedic trauma, providing patients with fracture fixation options that are metal-free and delivered in a minimally-invasive manner,” said Peter Markham, President, CEO and a co-founder of CBSET. “We are proud to have helped IlluminOss validate its novel technology. Since 2006, we have set the medtech gold standard for cutting-edge preclinical science, helping more than 400 companies transform their early-stage concepts into innovative therapies.”