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Capital Hilton

28 oct 2024 8:30 a.m. - 30 oct 2024 12:40 p.m.

1001 16th Street NW, Washington, DC 20036-5794

DIA/FDA Oligonucleotide-Based Therapeutics Conference

Session 6 Track 3: CMC Considerations in Development of mRNA-based Therapeutics

Session Chair(s)

Brian  Doyle

Brian Doyle

Senior Director, Technical Development

Moderna, United States

The breadth of mRNA-based vaccines in clinical and commercial development has continued to mature beyond SARS-CoV-2 vaccines, with the platform nature of mRNA supporting common CMC principles between products. As the landscape of mRNA-based therapeutics in development expands and evolves, thoughtfully adapting principles from mRNA-based vaccines to meet the unique CMC requirements of therapeutic development across diverse therapeutic areas will be needed. This session will include industrial and regulatory perspectives on CMC challenges specific to mRNA-based therapeutics and opportunities to efficiently support their development.

Learning Objective :
  • Compare differences in technical requirements and regulatory expectations between vaccines and therapeutics which warrant differentiated development strategies
  • Discuss how platform principles which have accelerated the development of mRNA-based vaccines can be adapted to the development of mRNA-based therapeutics

Speaker(s)

Xin (Jack)  Yu, PhD

Expanding Horizons: Navigating CMC Challenges and Opportunities for mRNA Therapeutics Beyond Vaccines

Xin (Jack) Yu, PhD

Moderna, United States

Vice President, CLinical Development

Eric A Levenson, PhD, MS

Advancing mRNA Vaccine Specifications to Support mRNA Therapeutics

Eric A Levenson, PhD, MS

FDA, United States

Biological Reviewer

Andreas  Kuhn, PhD

Panelists

Andreas Kuhn, PhD

Biontech SE, Germany

Senior Vice President RNA Biochemistry & CMC Development

Silke  Schüle, PhD

Panelists

Silke Schüle, PhD

Paul-Ehrlich-Institute, Federal Agency of Vaccines and Biomedicines, Germany

Scientific Assessor

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