Dana Solutions part of HESI U01 award from the FDA to study cardiac failure modes
Subaward to Dana Solutions will support the application of Artificial Intelligence for cardiac drug safety testing
Palo Alto, CA (PRWEB) July 22, 2019: Dana Solutions announced today that it will receive a subaward from the Health and Environmental Sciences Institute (HESI) as part of a multi-year U01 grant from the FDA. The grant, titled “Evaluation of Integrated Human-Relevant Approaches to Identify Drug Induced Cardiovascular Liabilities,” will support the funding and management of novel, in vitro experimental studies to develop targeted mechanistic data to inform drug safety assessment for key cardiac failure modes.
Under the U01 subaward, Dana Solutions, in partnership with HESI and US FDA, will use state-of-the-art analytical tools for cardiac drug safety testing. Specifically, they will apply and validate their image-based artificial intelligence (AI) platform, PhenoTox, to quantify drug-induced structural changes in human cardiac cell culture models. In collaboration with other grant sub-awardees and FDA partners, PhenoTox will be applied to study multiple cardiac failure modes, including cardiomyocyte injury. The project is expected to begin in September 2019.
About Dana Solutions LLC:
Dana Solutions develops Artificial Intelligence solutions for the life sciences industry. We partner with companies in medical devices and biotechnology, as well as academia and government institutions, to develop breakthrough products and enable new scientific discoveries.