Already a DIA Member? Sign in. Not a member? Join.

Sign in

Forgot User ID? or Forgot Password?

Not a Member?

Create Account and Join

San Diego Convention Center

Jun 23, 2019 2:30 PM - Jun 27, 2019 6:00 PM

111 W Harbor Drive, , San Diego, CA 92101 , USA

DIA 2019 Global Annual Meeting

Join thousands of your peers at the life sciences event of the year!

Immuno-Oncology Product Development: Overcoming Scientific and Regulatory Challenges

Session Chair(s)

Laurie  Iciek, PhD

Laurie Iciek, PhD

Senior Consultant, Nonclinical

Biologics Consulting, United States

The development of immuno-oncology products has spanned decades, culminating in approvals for the use of immune modulating cytokines, monoclonal antibodies, fusion proteins, genetically modified T cells, cancer vaccines and oncolytic vectors, for the treatment of cancer. Currently there are hundreds of immuno-oncology products in clinical trials.

This session will provide an overview of immuno-oncology products, highlighting the relevant preclinical safety regulations and potential safety concerns ascribed to different categories of products. Preclinical development challenges, such as, selecting the relevant pharmacology and toxicology models, distinguishing pharmacologic from toxicologic responses, and justifying first in human dose, will be discussed. Case examples highlighting the preclinical testing strategies that are being applied to evaluate the pharmacology and safety of immuno-oncology drugs will also be presented.

Learning Objective : Describe immuno-oncology products, including the potential safety concerns ascribed to different immunotherapeutic modalities; Identify the regulatory requirements (and/or challenges) associated with preclinical safety evaluation for different modalities of immuno-oncology drugs; Discuss the preclinical testing strategies that are being applied to evaluate the pharmacology and safety of immuno-oncology products through case study presentations.

Speaker(s)

Karin  Staflin, PhD

New Challenges for Developing HER2-Targeted Cancer Immunotherapeutics

Karin Staflin, PhD

Genentech, A Member of the Roche Group, United States

Senior Scientist

Simone  Nicholson, PhD

Strategies for Preclinical Safety Assessment of Immune-Oncology Biologics

Simone Nicholson, PhD

AstraZeneca, United States

Toxicologist

Theresa  Sweeney, PhD

Challenges in Predicting Animal-to-Human Safety for Immune-Stimulatory Agents from Toxicology Studies

Theresa Sweeney, PhD

Nektar Therapeutics, United States

Vice President, Safety Assessment

Have an account?

Be informed and stay engaged.

Don't miss an opportunity - join our mailing list to stay up to date on DIA insights and events.