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Prior to joining Tarsa, Dr. Gilligan held positions of increasing responsibility for nearly 30 years at Unigene, where he led the development of the oral calcitonin product now licensed to Tarsa. He serves as vice president of product development at Unigene, where he was project leader for the oral and nasal calcitonin programs, as well as the oral parathyroid hormone and site-directed bone growth programs. Dr. Gilligan was responsible for leading the clinical programs and successful U.S. and European regulatory registrations for the nasal calcitonin product Fortical® Nasal Spray and the injectable calcitonin product Forcaltonin® Injection. Dr. Gilligan holds a Ph.D. in pharmacology toxicology from the University of Connecticut and a master’s degree in international business from the Stillman School of Business at Seton Hall University.
Dr. Krause has over 20 years of pharmaceutical industry experience. Prior to Tarsa, he served as chief medical officer and senior vice president and head of R&D at Zelos Therapeutics, which develops osteoporosis therapies. Earlier, Dr. Krause was executive vice president and chief medical officer of Vicuron Pharmaceuticals, which was acquired by Pfizer. Previously, Dr. Krause held positions of increasing responsibility at GlaxoSmithKline and its predecessor companies, leading a number of worldwide clinical development groups and serving as vice president of medical strategy and cross-therapeutic affairs. Earlier in his career, Dr. Krause spent a decade in the practice of internal medicine. Dr. Krause holds an M.D. from Temple University School of Medicine and a B.A. from Pennsylvania State University. He has authored over 40 scientific publications and abstracts and is a Fellow of the American College of Physicians.
Dr. Wicks has over 25 years’ experience in regulatory strategic planning and execution. Prior to joining Tarsa, Dr. Wicks was vice president of regulatory affairs and quality assurance at Mt Cook Pharma. Previously, he served as vice president of regulatory affairs/acting vice president of medical affairs at Odyssey Pharmaceuticals. Prior to Odyssey, Dr. Wicks was senior director, global regulatory affairs at Purdue Pharma. Previously, Dr. Wicks served in positions of increasing responsibility at several sanofi-aventis predecessor companies, including vice president of regulatory affairs at Sanofi, where he played a key role in the regulatory strategy that led to approval of Plavix® and directed early clinical efforts for the bisphosphonate Skelid®. At the Rorer/Armour companies, (predecessors to Aventis) he led a team responsible for the registration of salmon calcitonin in Japan. Dr. Wicks holds a Ph.D. in physiology from Georgetown University and a B.S. in biology from the University of Maine. He completed an NIH post-doctoral fellowship at Georgetown University Medical Center.