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Date: Wednesday, June 18, 2025

Time: 11am ET

Products: Phoenix™

Summary

Anti-drug antibodies (ADAs), especially those with neutralizing potential, can significantly affect pharmacokinetics (PK) and complicate translational predictions. Understanding and accounting for neutralizing ADA early in drug development is critical for generating reliable PK models and accurate dose projections across species.

Join Certara’s expert-led session where we’ll explore how neutralizing ADAs impact PK, why these effects are often not translatable between species, and the risks of ignoring ADA in your nonclinical data package. Through real-world case studies, we’ll demonstrate how structural and covariate models, built in Phoenix® NLME can be used to support interspecies scaling and human dose prediction when neutralizing ADA is present or suspected.

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Key topics include:

  • What are neutralizing ADAs and how do they affect pharmacokinetics?
  • Challenges in translating ADA effects from nonclinical to clinical data
  • Case studies highlighting modeling strategies to manage ADA-driven variability
  • Application of Phoenix NLME for interspecies scaling and human dose projections

Why you should attend:

  • Gain a deeper understanding of neutralizing ADA and its impact on PK in biologics development
  • Learn how failing to account for ADA in nonclinical studies can compromise your translational models
  • See real-world examples of how to model ADA effects effectively using Phoenix NLME
  • Walk away with actionable insights to strengthen interspecies scaling and human dose prediction

Speakers:

Elliot Offman BSc, Pharm, MSc, PhD

Vice President, Clinical Pharmacology & Translational Medicine
Certara Drug Development Solutions

Martin Beliveau, PhD

Vice President, Quantitative Science Services
Certara Drug Development Solutions

Keith Nieforth, PhD

Senior Director, Pharmacometrics Software
Certara

Register now