\"We have designed a product to attempt to overcome the greatest challenge facing other neural interfaces: chronic brain tissue scarring,\" said Thomas Oxley, MD, PhD, founder and CEO of Synchron. <\/p>\n
\"We aim to provide a safe way for patients with severe paralysis to achieve direct brain control of assistive devices. Successful completion of this funding round allows us to commence human studies.\" <\/p>\n
The Stentrode system is small and flexible enough to safely pass through curving blood vessels in a procedure called cerebral angiography, eliminating the need for open brain surgery and direct contact with brain tissue. By using blood vessels to deliver the technology to the brain and house it there, the technique may reduce risk of brain tissue rejection of the device, which has been a significant problem for other techniques. <\/p>\n
Pre-clinical studies published in Nature Biotechnology have demonstrated the Stentrode's ability to pick up high-frequency electrical data emitted by the brain. This level of brain recording has previously required invasive electrode implantation through the skull. <\/p>\n
According to a global report from McKinsey & Co., in advanced economies, there are 50 million people with impaired mobility due to paralysis. A new industry of 'robotic human augmentation' promises to provide novel solutions to patients with paralysis to achieve enhanced and independent control of their environment. <\/p>\n
The Stentrode was initially developed through a multi-departmental collaboration at the University of Melbourne, The Florey Institute of Neuroscience and Mental Health, and the Royal Melbourne Hospital, Australia. The Australian company SmartStent was spun out in 2012 and was wholly acquired by Silicon Valley-based Synchron in 2016. Early funding for the device was provided from the U.S. Department of Defense, including DARPA and theU.S. Office of Naval Research Global. <\/p>\n
Dr. Oxley and Nicholas Opie, PhD, Synchron co-founder and chief technology officer, also received substantial funding from the Australian National Medical Health and Medical Research Council (NHMRC) to the University of Melbourne Vascular Bionics Laboratory to develop the technology. <\/p>\n
About Synchron, Inc.Based in Silicon Valley, Synchron, Inc. is an innovative medical device company focused on the development of minimally invasive neuromodulation technology solutions. Synchron is developing the world's first endovascular neural interface, the StentrodeTM. Development of this technology platform has been funded in part by grants from the U.S. Defense Advanced Research Projects Agency (DARPA) and U.S. Department of Defense (DoD). The company is targeting paralysis due to a range of neurological conditions as a first application. Other applications may include epilepsy and movement disorders. <\/p>\n
Stentrode is a trademark of Synchron, Inc. <\/p>\n
About NTI Neurotechnology Investors (http:\/\/themdadvantage.com<\/a> ) draws on the knowledge and investment power of over 100 neurology, neurosurgery and radiology specialists from across the U.S. to perform targeted investments in high potential technologies. <\/p>\n To view the original version on PR Newswire, visit:http:\/\/www.prnewswire.com\/news-releases\/synchron-inc-secures-10-million-in-series-a-financing-round-300433942.html<\/a> <\/p>\n SOURCE Synchron Inc. <\/p>\n http:\/\/www.synchronmed.com<\/a><\/p>\n <\/p>\n Original post:<\/p>\n Synchron Inc. Secures $10 Million in Series A Financing Round - PR Newswire (press release)<\/a><\/p>\n","protected":false},"excerpt":{"rendered":" \"We have designed a product to attempt to overcome the greatest challenge facing other neural interfaces: chronic brain tissue scarring,\" said Thomas Oxley, MD, PhD, founder and CEO of Synchron. \"We aim to provide a safe way for patients with severe paralysis to achieve direct brain control of assistive devices. Successful completion of this funding round allows us to commence human studies.\" The Stentrode system is small and flexible enough to safely pass through curving blood vessels in a procedure called cerebral angiography, eliminating the need for open brain surgery and direct contact with brain tissue Continue reading