ISSX

October 11-14, 2026 | San Francisco, CA | Booth 405

The ISSX meeting provides an exceptional opportunity to learn, network, and exchange ideas with researchers from around the world. Interact with a broad representation of international researchers and other scientists who are gaining a deeper understanding of drug metabolism and pharmacokinetics.

Breakfast Symposium

Symposium Title: Advancing Peptide Therapeutics: Tackling Biotransformation and Oral Absorption Challenges

Date: Tuesday, October 13
Time: 7:15am – 8:15am
Location: Imperial 

Presenter:

Peng Li

Peptide Biotransformation

Jianping Sun

Oral Peptide Absorption

Abstract: Therapeutic peptides present distinct DMPK challenges, including complex biotransformation and limited intestinal permeability. This symposium will highlight two complementary approaches: advanced LC-HRMS and TidesID for peptide metabolite characterization, and an optimized Caco-2/in vivo PK workflow for permeation-enhancer screening and oral absorption assessment.

Learning Objectives:

  • Understand key challenges in peptide biotransformation and metabolite identification.
  • Learn how LC-HRMS and TidesID support peptide metabolite characterization.
  • Explore Caco-2–based permeation enhancer screening for oral peptides.
  • See how in vitro and in vivo PK data can guide peptide development.

 

Thought Leader Partner Presentation

Title: Physicochemical Property-Guided Formulation Screening to Optimize the Preclinical Pharmacokinetic Profiles of PROTAC Degraders

Date: Monday, October 12
Time: 9:40am – 9:55am
Location: Grand Ballroom (Exhibit Hall)

Presenter:

Quanli Feng

Abstract: As bRo5 drugs play an increasingly crucial role in treating complex diseases but have poor oral pharmacokinetics, it is significantly important to establish a more rapid screening platform to provide essential guidance for molecular modification, By combining in vitro data, such as physicochemical property data EPSAExposed Polar Surface Area, solubility, Log D, and in vitro ER(efflux ratio) data, it guides the screening of appropriate preclinical excipients,  thereby efficiently increasing the in vivo exposure of preclinical oral PROTACs.

Thought Leader Partner Presentation

Title: Visualizing Maternal and Fetal Distribution Using Quantitative Whole-Body Autoradiography

Date: Tuesday, October 13
Time: 1:30pm – 1:45pm
Location: Grand Ballroom (Exhibit Hall)

Presenter:

Leah Lake

Short description of the talk: Quantitative whole-body autoradiography (QWBA) can be used not only to assess drug distribution across tissues and organ systems, but also to evaluate how compounds distribute to fetuses, cross the placental barrier, and interact with the maternal environment in which the fetuses develop. We evaluated the distribution of radioactivity in two pregnant female Sprague Dawley rats and their fetuses following test article administration.  Selected tissues from the adult female rats and associated fetuses were analyzed to characterize differences in distribution between maternal and fetal compartments using QWBA methodologies, supporting its application in evaluating placental transfer.