NEWARK, Del.--(BUSINESS WIRE)--iBio, Inc. (OTCBB:IBPM) announced today that the U.S. Food and Drug Administration (FDA) accepted an Investigational New Drug (IND) application filed for a vaccine candidate made with the Company’s proprietary transformative technology, the iBioLaunch™ technology platform. The candidate vaccine was manufactured by iBio’s research collaborator, Fraunhofer Center for Molecular Biotechnology (FCMB), in its cGMP pilot manufacturing facility in Newark, Delaware. The Company expects human clinical trials based upon this IND to commence promptly. The primary endpoint of the study will be safety, and immunogenicity data will also be collected.
