World Federation of Hemophilia/Consultant
World Federation of Hemophilia/Consultant
La Jolla, California, United States
Glenn Pierce, MD, PhD, Vice President Medical for the World Federation of Hemophilia and Independent Consultant.
Glenn Pierce has more than 35 years of experience in bench-to-bedside research and development with several public and private biopharmaceutical companies, including Biogen, Bayer, Inspiration, Avigen, Selective Genetics, and Amgen. At Biogen, Dr. Pierce served as senior vice president of hematology, cell and gene therapies, with overall R&D responsibility for hemophilia and hemoglobinopathies and led the research and clinical development of the first extended half-life FVIII (Factor VIII) and FIX (Factor IX) Fc fusions. He co-founded Ambys Medicines, a cell and gene therapy liver regeneration start-up, where he served as chief medical officer and most recently served as interim CSO of Voyager Therapeutics, a neurodegenerative gene therapy company, where he serves on the board of directors.
Dr. Pierce currently serves as vice president, medical, with the World Federation of Hemophilia (WFH). He serves on the U.S. medical and scientific advisory council (MASAC), and previously served on the board of directors and as board president of the National Bleeding Disorders Foundation (NBDF) (previously NHF). Dr. Pierce spearheaded the initiation of the expanded WFH humanitarian aid program providing clotting factor distribution to 25,000 people with hemophilia in 74 lower income countries. He also co-developed the My Life Our Future (MLOF) program in the U.S. to genotype more than 10,000 individuals in the U.S. bleeding disorder community.
OC 30.1 - Seven-year follow-up of valoctocogene roxaparvovec gene therapy for haemophilia A
Monday, June 24, 2024
09:30 – 09:45 ICT
PB0500 - Communicating gene editing in hemophilia: development of a universal lexicon
Monday, June 24, 2024
13:45 – 14:45 ICT
PB0537 - Development of novel gene editing lexicon for hemophilia: methodology and results
Monday, June 24, 2024
13:45 – 14:45 ICT
SSC 018.2 - Who should be treated with gene therapy for hemophilia A and B?
Monday, June 24, 2024
16:35 – 16:45 ICT