Wednesday, February 4, 2026

Nonclinical evaluation of HS630, a proposed biosimilar of trastuzumab emtansine: affinity, pharmacokinetics, and immunogenicity.

Authors: Jiang H, Che J.

DOI: 10.3389/fphar.2025.1698727

Abstract Summary

HS630, a biosimilar candidate for trastuzumab emtansine (T-DM1/Kadcyla®), demonstrates comparable binding affinity to HER2 receptors and similar pharmacokinetic profiles in preclinical studies. Testing in tumor-bearing mice and cynomolgus monkeys showed matching drug concentrations and distribution patterns, with no immunogenicity concerns detected. These findings support HS630’s biosimilarity to Kadcyla® and provide critical data for regulatory approval.

Why Brain? 🧠

HS630 demonstrates comparable binding affinity, pharmacokinetics, and immunogenicity to trastuzumab emtansine in preclinical studies, supporting its development as a biosimilar for HER2-positive cancer treatment.

License: CC BY.


The image is AI-generated for illustrative purposes only. Courtesy of Midjourney.

share this recipe:
Facebook
X
Email
Print

Still hungry? Here’s more