Terrie Kellmeyer, PhD, Senior Vice President of Clinical Development, brings over 28 years of experience in the pharmaceutical industry and has held executive leadership positions in Clinical Development, Regulatory Affairs, Clinical Operations, and Medical Affairs across multiple therapeutic areas. Dr. Kellmeyer has played a key role in overall regulatory strategy and has led and contributed to the submission of multiple successful New Drug Applications to the FDA and Marketing Authorization Applications to the European Medicines Agency (EMA), among them OLPRUVA® (sodium phenylbutyrate), REZDIFFRA® (resmetirom), BYETTA® (exenatide injection), SYMLIN® (pramlintide acetate), and OCALIVA® (obeticholic acid). Prior to joining Anavex Dr. Kellmeyer held strategic leadership positions, including Head of Global Regulatory Affairs at Madrigal Pharmaceuticals, and positions of increasing responsibility at Intercept Pharmaceuticals, Amylin Pharmaceuticals, Gen-Probe, and most recently as Group Vice President of Clinical Development at Acer Therapeutics. Dr. Kellmeyer received her BS degree in Biotechnology from Rochester Institute of Technology, a PhD in Molecular Biology from SUNY Syracuse, and did a Post-Doctoral Fellowship at the University of Rochester.