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Session 8: Hot Topics
Session Chair(s)
Patrik Andersson, PhD
Senior Director, AstraZeneca R&D, Sweden
Susanne Brendler-Schwaab, DRSc
Head of Unit, Senior Toxicologist, ICH S13, BfArM, Germany
The Hot Topics session will provide an overview of three areas that will provide clarity and likely influence the way of working with oligo projects. 1. An overview of the draft ICH S13 draft guideline on nonclinical safety of oligonucleotides that shortly after the meeting will be published for public consultation; 2. How will the regulatory roadmaps for New Approach Methodologies (NAMs) influence oligo R&D and 3. How can use of AI be applied to oligo therapeutics to increase throughput and success rate of oligo projects.
ICH S13: Nonclinical Safety Evaluation of Oligonucleotide-Based Therapeutics
Susanne Brendler-Schwaab, BfArM
NAMs to Support Oligonucleotide Development and Regulatory Submission and Review: An FDA/CDER/OND Perspective
Jia Yao, FDA
AI in Oligonucleotide Discovery
Daniel Butnaru, Roche
Learning Objective : At the conclusion of this session, participants should be able to: - Mention key themes in the draft ICH S13 guideline on nonclinical safety for oligos
- Discuss specific situations where a NAMs approach could be applied to an oligo project
- Suggest potential areas in the oligo project Drug Discovery and Development value chain where application AI could add significant value
Speaker(s)
ICH S13: Nonclinical Safety Evaluation of Oligonucleotide-Based Therapeutics
Susanne Brendler-Schwaab, DRSc
Head of Unit, Senior Toxicologist, ICH S13, BfArM, Germany
NAMs to Support Oligonucleotide Development and Regulatory Submission and Review: An FDA/CDER/OND Perspective
Jia Yao, PhD, RAC
Senior Pharmacologist, Office of New Drugs, CDER, FDA, United States
AI in Oligonucleotide Discovery
Daniel Butnaru, PhD
Senior Principal Scientist Computational Design, Roche, Switzerland
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