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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 4 Track 3: Demonstrating Comparability for Oligonucleotides Therapeutics

Session Chair(s)

Daniel  Capaldi, PhD

Daniel Capaldi, PhD

Vice President, Analytical and Process Development

Ionis Pharmaceuticals, Inc, United States

Fran  Wincott, PhD

Fran Wincott, PhD

President

Wincott & Associates, LLC, United States

Oligonucleotide therapeutics are larger and more complex than traditional small molecule drugs. Consequently, the task of demonstrating comparability of materials made by different manufacturing processes, may be more challenging for oligonucleotide therapeutics than for small molecule drugs. The session will include presentations from regulatory authorities, and industry scientists. The presentations will be followed by a panel discussion. Topics for discussion may include how to define comparability, the types of chemical and physicochemical characteristics that should be evaluated, analytical methods for assessing comparability, and the potential impact of observed differences in chemical and physicochemical properties.

Learning Objective : At the conclusion of this session, participants should be able to:
  • Define comparability requirements for oligonucleotide therapeutics
  • Discuss how to evaluate the impact of manufacturing changes on oligonucleotide therapeutics
  • Discuss how to demonstrate comparability between generic and brand name oligonucleotide therapeutics

Speaker(s)

Deyi  Zhang, PhD, MS

Comparability in Generic Oligonucleotide Drug Development: Regulatory Considerations and Case Studies

Deyi Zhang, PhD, MS

FDA, United States

Senior Chemist, Office of Generic Drugs

Carolyn  Mazzitelli, PhD

Demonstrating Comparability of Oligonucleotide Therapeutics Following Manufacturing Changes

Carolyn Mazzitelli, PhD

Ionis Pharmaceuticals, United States

Executive Director, Analytical Development and Quality Control

Lawrence  Perez, PhD

Panelist

Lawrence Perez, PhD

FDA, United States

Senior Pharmaceutical Quality Assessor, CDER

Lubo  Nechev, PhD

Panelist

Lubo Nechev, PhD

Alnylam Pharmaceuticals, United States

Chief CMC Officer

Lori  Troup

Panelist

Lori Troup

Novo Nordisk, United States

Director, Analytical Development

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