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Session 4 Track 1: Translational Safety of Genetically Targeted Oligonucleotides: Managing Mechanistic Risks, Immunogenicity, and AOC Platforms
Session Chair(s)
Sydney Stern, PHD, MS
Associate Director
BeOne Medicines, United States
This session will explore the evolving landscape of translational safety for genetically targeted oligonucleotide therapeutics, with a focus on understanding, assessing, and mitigating class-specific and emerging risks. We will begin by framing the key mechanistic safety considerations associated with oligonucleotides, including class-related adverse events such as liver function test (LFT) elevations, thrombocytopenia, and proteinuria. Building on this foundation, speakers will examine approaches to evaluating and de-risking immunogenicity and QTc liability, drawing on clinical and long-term data from GalNAc-siRNAs as a well-characterized platform. The session will then address safety challenges associated with newer modalities, including linker-containing antibody–oligonucleotide conjugates (AOCs), and discuss how lessons learned from established platforms can inform risk assessment for emerging chemistries, including CNS-targeted approaches. Overall, this session aims to foster shared learning and advance strategies to proactively manage safety across the next generation of oligonucleotide therapeutics.
Learning Objective : At the conclusion of this session, participants should be able to: - Compare strategies to de-risk class-specific safety profiles
- Identify lessons learned from well-characterized GalNAc-siRNAs
- Apply how these insights can be applied to AOCs
Speaker(s)
Comprehensive Immunogenicity Assessment of GalNAc-siRNAs: Clinical and Long-Term Data Insights
Chaejin Kim, PHARMD, PHD, MPH
Alnylam Pharmaceuticals, United States
Sr Scientist
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