The company's main focus is on a 100-patient clinical trial to convince the rehabilitation community of Rex's benefits, with ethics committee approval expected this month and the first patient recruited soon after. It is also bringing forward a US clinical trial to secure FDA clearance of the robotic exoskeletons for at-home use in the US by the end of next year.
"In the medium-term, we expect that evidence of clinical benefit will underpin commercial success," Simon said.
Manufacturing efficiencies in Auckland have cut the unit materials cost of a Rex device by more than a quarter since September. The priority now is on producing adequate numbers to meet distributor demand for product demonstrations.
Research and development work is progressing on Rex 3, the next-generation re-modelled and lower cost product that is due for release in 2017. Discussions are also under way with a number of clinics about using Rex technology in fields other than spinal injury, such as stroke, traumatic brain injury and multiple sclerosis, Simon said.
Rex raised 10 million in its reverse takeover and listing in May, to fund the roll-out of its device. As at November 30 the company had £5.8 million in cash and that had fallen to £4.98 million by the end of January.
Before the May listing, Rex received $2.9 million in government funding, a condition of which requires production to stay here until 2017.
Rex Bionics
•Makes exoskeletons that allow wheelchair-bound people to walk.
•Listed on the London Stock Exchange's AIM market.
•Received government funding, which required production to stay in NZ until 2017.
•Widened full-year loss to £3.56 million from £480,000.