CF Foundation | Brady Brock's Story: Genetic Therapy Clinical Trials
Автор: Cystic Fibrosis Foundation
Загружено: 2024-09-26
Просмотров: 861
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We believe that genetic therapies offer the best hope for a treatment for the underlying cause of cystic fibrosis that could benefit everyone with CF, regardless of their mutations.
Brady Brock, an adult with cystic fibrosis who has two nonsense mutations, shares his experience participating in a clinical trial for genetic therapies. Justin Anderson, MS, CCRC, a clinical research coordinator at the University of Alabama, explains his experience helping conduct clinical trials for genetic therapies and what excites him about the future of this research.
This video was originally featured in Plenary 1 of the 2024 North American Cystic Fibrosis Conference.
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