Dr. Mannix brings more than 30 years of pharmaceutical regulatory affairs experience in positions of increasing responsibility at Pharmacia, Amersham Health, BMS, EMD Serono, Kyowa Hakko Kirin, and MacroGenics across multiple therapeutic areas, but with a focus in oncology. Within these companies, he was involved with the development and approval of a number of oncology drugs, including Camptosar® (irinotecan), Aromasin® (exemestane), Ellence® (epirubicin), Yervoy® (ipilimumab), Poteligeo® (mogamulizumab) and Margenza® (margetuximab). Dr. Mannix has a Bachelor of Science in biology and Ph.D. in molecular biology from the University of Notre Dame and completed an NIH-sponsored post-doctoral fellowship at The Ohio State University Comprehensive Cancer Center.