ADME and Bioanalytical Strategies for ADCs: Challenges, Emerging Technologies, and Regulatory Considerations

DATE
September 18, 2025
TIME
8:00 a.m. PDT, 11:00 a.m. EDT, 16:00 BST, 17:00 CEST - Duration: 60 Minutes

Overview

Antibody-drug conjugates (ADCs) are transforming cancer treatment, but their development brings unique challenges in the DMPK field, including ADME, bioanalysis, and regulatory registration. This webinar explores integrated DMPK and bioanalytical strategies for ADC discovery and development, grounded in recent analytical advances, global guidelines, and real-world experience.

Topics include bioanalytical approaches for assessing pharmacokinetics and biotransformation of ADCs, challenges associated with ADC bioanalysis, and opportunities enabled by emerging technologies. In addition, an ADME characterization decision tree and associated experimental approaches, integrated with regulatory considerations, will be presented to support the design and execution of MIST, DDI evaluation, and animal biotransformation studies of novel payloads. Advanced LC-MS techniques for untargeted profiling of payload-containing components and the investigation of ADC biotransformation will also be discussed.

Whether you’re advancing an ADC program or addressing ADME and bioanalytical issues associated with ADCs, this webinar offers practical insights and technical solutions to support ADC optimization, development, and regulatory goals.

Key Learning Objectives:
  • ADME study strategy and decision tree for characterizing novel payloads
  • Untargeted LC-HRMS method for studying payload release 
  • HR Orbitrap MS for in-depth characterization of ADC biotransformation
  • Generic reagent and targeted 2D-LC-MS/MS for highly sensitive quantitative analysis 
  • Regulatory aspects of ADME and bioanalytical studies of ADCs
Who Should Attend:
  • Laboratory managers
  • New product developers
  • DMPK and bioanalytical scientists
  • ADC discovery and development teams
  • Preclinical and toxicology professionals
  • Clinical pharmacology and regulatory affairs specialists
  • Project managers

Brought to you by:
BioDuro logo

Speakers

Mingshe Zhu, Ph.D.
Scientific Advisor of DMPK,
BioDuro
Jintang He, Ph.D.
Senior Principal Scientist,
Genentech
Alexandra Taylor
Contributing Editor,
C&EN Media Group

Registration

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