discovering and developing innovative solutions to treat brain disorders. Philips will be responsible for the development and manufacturing of the handheld test. The test will be based on Philips’ Minicare system, which is currently under development. Janssen will be responsible for the clinical studies to validate the test, as well as the commercialization of the final product.
“Our technology can play an important role in the management of chronic diseases in the hospital and the home,” said Frans van Houten, CEO Royal Philips. “Better care for patients with neuropsychiatric disorders is a key driver to improve patient outcomes and lower healthcare costs. The collaboration with Janssen is a great example of our open innovation business model, combining their strength in neuroscience with the biosensor technology in our Minicare I-20 platform.”
Mr. Van Houten added: “Going forward, I firmly believe that the Minicare system consisting of the analyzer and application-specific cartridges and software, can be tailored to a wide range of other pharmaceuticals.”
The blood test will be based on Philips’ Minicare I-20 system for immunoassays, which consists of a handheld analyzer, dedicated software and a single use, disposable cartridge containing the application specific test. Based on Philips’ proprietary biosensor technology, the Minicare I -20 system is being developed to detect multiple target molecules at low concentrations within the same blood sample and to show the results on the analyzer display within minutes.
The Minicare activities are part of Philips’ Handheld Diagnostics business that has its headquarters and manufacturing lines at the High Tech Campus in Eindhoven, the Netherlands. The business will be expanding its production capacity in light of the new partnership.