On May 21, 2020 Transcenta, a global biotherapeutics company that fully integrates antibody-based biotherapeutics discovery, development and manufacturing, reported that it will present preclinical data of TST001, a humanized Claudin 18.2 (CLDN18.2) monoclonal antibody developed by its subsidiary Mabspace Biosciences, in a poster during the 2020 American Association for Cancer Research (AACR) (Free AACR Whitepaper) Virtual Annual Meeting II, being held from June 22-24 (Press release, Transcenta, MAY 21, 2020, View Source [SID1234558401]).
Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:
Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing
Schedule Your 30 min Free Demo!
Poster Presentation Details:
Title:
The preclinical characterization of TST001, a novel humanized anti-claudin18.2 mAb with enhanced binding affinity and anti-tumor activity.
Abstract Control Number: 2148
Permanent Abstract Number: 5183
Session Category: Experimental and Molecular Therapeutics
Session Title: Cell Surface Antigens and Receptors as Drug Targets
Lead Author: Fei Teng
About TST001
TST001 is a humanized monoclonal antibody targeting human Claudin18 isoform 2 (CLDN18.2). CLDN18.2 is the tight junction protein with expression strictly confined to differentiated epithelial cells of the gastric mucosa. Published data indicates that CLDN18.2 is often overexpressed in gastroesophageal, pancreatic, lung, and other solid tumors, which makes it an attractive Antitumor therapeutic target. As a humanized monoclonal antibody with high binding affinity to CLDN18.2, TST001 kills tumor cells mainly by antibody-dependent cellular cytotoxicity (ADCC). In preclinical studies, TST001 is efficacious in multiple tumor animal models, and well tolerated in GLP toxicology studies. Transcenta has received IND clearance from FDA and NMPA for initiating clinical trials for TST001.