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Designing innovative preclinical data packages to inform the need for long-term follow-up in gene therapy trials and the possibility of delayed adverse events

15 Apr 2025
Gene Therapy Development
  • How do we alter/construct preclinical data packages to assess the risk of delayed adverse events and the need for long term follow-up?
  • Understanding the risk of delayed adverse events for integrating and gene-editing based therapies in novel products
  • Innovations in assay development to better understand PK/PD,  persistence, and the impact of long term modification of cells with in vivo gene therapy
Industry Expert
Neal van Hoeven, Vice President Preclinical - Calabetta Bio