Dr. try thisCoric and Dr. William Bockenek, Chief Medical Officer at Carolinas Rehabilitation, are Co-principal Investigators at this site. Implantation of the Neuro-Spinal Scaffold went smoothly and the patient is doing well, Dr. Coric said. I have now implanted five patients with different injury types and locations, and the implantation procedure has been consistently uncomplicated. I look forward to following this most recent patients progress. Mark Perrin, InVivos Chief Executive Officer and Chairman, said, We now have ten INSPIRE patients enrolled and in follow up, which is an important milestone in this study designed to enroll 20 evaluable patients. We thank Dr. Coric and his team for having enrolled five patients at their site, and look forward to continuing to make progress toward full enrollment. For more information, please visit the companys ClinicalTrials.gov registration site: http://clinicaltrials.gov/ct2/show/study/NCT02138110 About the Neuro-Spinal Scaffold Implant Following acute spinal cord injury, surgical implantation of the biodegradable Neuro-Spinal Scaffold within the decompressed and debrided injury epicenter is intended to support appositional healing, thereby reducing post-traumatic cavity formation, sparing white matter, and allowing neural regeneration across the healed wound epicenter. The Neuro-Spinal Scaffold, an investigational device, has received a Humanitarian Use Device (HUD) designation and currently is being evaluated in the INSPIRE pivotal probable benefit study for the treatment of patients with complete (AIS A) traumatic acute spinal cord injury. About InVivo Therapeutics InVivo Therapeutics Holdings Corp.
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