Ed Kaye’s decades-long career has always centered around helping children with severe diseases, resulting in seven approved medicines that have helped change the lives of tens of thousands of people. Trained in pediatrics, pediatric neurology and biochemical genetics with a B.S. in biology from Loyola University and an M.D. from the Loyola University Stritch School of Medicine, he was on the research staff at Massachusetts General Hospital and Tufts University Medical Center and was the chief of biochemical genetics at the Children’s Hospital of Philadelphia. He was on the pediatric neurology staff at Boston Children’s Hospital until 2021.
In 2001, Dr. Kaye started the next phase of his career where he focused on translating promising science into new medicines for severe genetic diseases. He spent 10 years at Genzyme Corporation, most recently as group vice president of clinical development, where he supervised clinical research in programs focused on lysosomal storage disease and genetic neurological disorders. At Genzyme, Dr. Kaye also held various roles, including vice president of medical affairs for lysosomal storage diseases, vice president of clinical research and interim head of PGH global medical affairs. In 2011, he joined Sarepta Therapeutics as Chief Medical Officer leading the drive to develop Exondys 51 a pioneering drug for Duchenne muscular dystrophy. He went on to serve as CEO of Sarepta in 2015, where he led the successful push to win FDA approval of Exondys 51. He also served on Sarepta’s Board of Directors. From 2017 to 2025, Dr. Kaye served as Stoke Therapeutics’ CEO and Director. He currently serves as a member of the Boards of Directors at Stoke, Cytokinetics, Inc., Avidity Biosciences and the Massachusetts Biotechnology Council.
Dr. Kaye earned his B.S. in biology from Loyola University and earned his M.D. at the Loyola University Stritch School of Medicine.