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» New regulatory playbook to guide AAV gene therapy development for rare diseases
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Drug Design, Drug Delivery & Technologies
New regulatory playbook to guide AAV gene therapy development for rare diseases
Feb. 7, 2024
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The Foundation for the National Institutes of Health (FNIH) has announced the online publication of the first playbook designed to help accelerate the development of adeno-associated virus (AAV) gene therapies for rare diseases.
BioWorld Science
Regulatory
Drug design, drug delivery and technologies
Gene therapy
U.S.
FDA
NIH
