Parker's Indego exoskeleton device may come to market within two years.
Cleveland, OH – Parker Hannifin Corp., a supplier of motion and control technologies, has entered into clinical trial agreements with four rehabilitation institutions in the United States to support the testing and development of the Indego exoskeleton.
Indego is a robotic exoskeleton or powered orthotic device that allows users to stand and walk, and holds great promise for affording people with paraplegia a new level of independence. The device was invented by a US university and Parker acquired the rights to develop it. Devices something like this are already in use; for example, Canadian athlete Rick Hansen uses one that enables the paraplegic to walk short distances (read a brief biography about him at http://www.rickhansen.com/Portals/2/Documents/RHBio_IntSec.pdf).
“Our objective is to bring Indego to market to enable people who were told they would never walk again to stand upright and walk and to provide a new level of independence,” said Achilleas Dorotheou, head of the human motion and control business unit for Parker.
Parker is currently developing a second-generation device for clinical trials starting in July 2014 to support submission for FDA approval. Pending regulatory approvals, Parker is targeting commercial launch of Indego in Europe in early 2015 and in the United States in 2016.
Parker has formalized agreements with the Rehabilitation Institute of Chicago; Kessler Foundation/Kessler Institute for Rehabilitation in West Orange, NJ; Rusk Rehabilitation at NYU Langone Medical Center in New York, NY; and Craig Hospital in Denver, CO. These institutions will work in concert with Shepherd Center in Atlanta, GA, which will continue as Parker’s lead rehabilitation centre for clinical testing of the device. Each of these institutions is currently ranked in the top ten US rehabilitation centres by US News & World Report.
“We have engaged in discussions with the FDA, payers and administrators to best position the commercial launch of Indego,” said Dorotheou. “With these agreements we will be working with the best and most respected rehabilitation clinicians and researchers in the country gathering evidence that demonstrates the safety of Indego and proves its tangible clinical and economic benefits.”
Parker aims at having Indego become the first powered exoskeleton or powered orthotic device to receive FDA approval and has been in discussion with the agency during the past year to determine the appropriate classification of the device and obtain input into the design of the clinical trials. The company is also working to secure the regulatory approvals and CE marking for Indego in Europe, which are expected by the end of 2014, and it is establishing partnerships with leading institutions in the region.
Neurorehabilitation expert Stefan Bircher, Ph.D., recently joined Parker as global market development manager for the human motion and control business unit.
In July 2014, Indego is expected to be made available by request to additional select US rehabilitation clinics to be included in clinical studies. These studies will build a body of evidence required for reimbursement coverage of Indego by public and private payers when the device becomes available for personal use in the future.
Indego is an investigational device and limited by law for investigational use only. To learn more, visit www.indego.com.