Leadership

Ms. Powell joined Tavanta Therapeutics in September 2019 and has 30 years of experience in the biopharmaceutical/ biotechnology industry. Prior to Tavanta she served as Chief Commercial Office at BioCryst, an emerging biotechnology company focused on commercializing innovative small molecules for rare diseases. Before this, she was Senior Vice President, North America, at CSL Behring. Throughout her 17-year career at CSL Behring, she assumed increasing responsibilities within the R&D, Business Development and Commercial functions of the organization. Ms. Powell has significant global experience serving as Vice President, Global Commercial Development and Head of Business Development & European Marketing, Head of Project and Portfolio Management and Head of Clinical Research. Ms. Powell also held positions within Glaxo Wellcome’s UK based commercial strategy and clinical research organizations. Ms. Powell serves on the Board of Directors for Progenity.

Dr. Malobisky brings over 30 years of executive leadership and global drug development to Tavanta Therapeutics. Most recently, Dr. Malobisky was the Senior Vice President, Global Regulatory Affairs, Quality, and Compliance at Achillion Pharmaceuticals where he led the successful regulatory and quality development of danicopan, for the treatment of the rare diseases paroxysmal nocturnal hemoglobinuria (PNH) and C3 Glomerulopathy (C3G). Under his leadership, danicopan was granted Breakthrough Therapy Designation by the Food and Drug Administration and PRIME designation by the European Medicines Agency. Previously, Dr. Malobisky was the Senior Vice President, Global Regulatory Affairs, Quality, and Pharmacovigilance at Karyopharm Therapeutics where he led their first successful New Drug Application submission for XPOVIO ® (selinexor) tablets for the treatment of adult patients with relapsed or refractory multiple myeloma. In addition to his experience in rare disease and biotechnology, Dr. Malobisky has also held positions of increasing responsibility at Sanofi, Roche Molecular Systems, and Hoffmann-LaRoche. After earning his Bachelor of Science degree in Microbiology from Penn State University, Dr. Malobisky earned his Masters degree in Regulatory Affairs and Quality Assurance from Temple University School of Pharmacy and his Ph.D. with distinction in Organization and Management from Capella University School of Business and Technology. Dr. Malobisky is also Regulatory Affairs Certified (RAC) and serves as an independent advisor to Allyx Therapeutics and ReNetX Bio, Inc.

Ms. Ferenczi has been with Tavanta Therapeutics since 2010. She began with Tavanta (then NanGenex) by leading the business development operations and was later promoted to Managing Director. Ms. Ferenczi now serves as General Manager, Europe. Prior to Tavanta, she worked at Genpact, a formerly GE owned company, that had established itself as one of Europe’s business services and technology solutions providers. Ms. Ferenczi has also served in a senior business development position at SOLVO Biotechnology and was responsible for the European sales operations of the company. Ms. Ferenczi graduated as a biomedical engineer from the University of Miami.

Ms. Whitfield brings over 25 years’ experience in the drug development arena to Tavanta Therapeutics with a track record of delivering programs from pre-clinical to late stage intended for large patient populations as well as for orphan/rare indications across a broad range of drug product formats intended for oral, inhaled, topical and parenteral administration routes. Most recently she held the position of Vice President, CDMO Services for Quotient Sciences working across the global sites supporting the integrated CMC and clinical platform. Ms. Whitfield has previously held leadership positions within Vectura, Elan, Quadrant Healthcare and Andaris, overseeing CMC activities which alongside formulation and analytical development included regulatory filings across the development phases.

Dr. Duus brings 15 years of clinical research experience in the biopharmaceutical industry to Tavanta Therapeutics, spanning early and late development across multiple therapeutic areas. Most recently, she served as Senior Director, Clinical Research & Strategy at Helsinn Therapeutics (U.S.), Inc. Over the 8 years at Helsinn, Dr. Duus led the clinical strategy for oncology-related compounds in development, contributed to global regulatory engagements, supported clinical operations and biostatistics, managed medical writing activities, and oversaw investigator-initiated and collaborative studies in the US. She also held positions of increasing responsibility at Akros Pharma Inc and Avantix Laboratories. After receiving an undergraduate degree in biology from the University of Delaware, Dr. Duus earned her PhD in pharmacology and molecular sciences from the Johns Hopkins University School of Medicine.