CB307: A Dual Targeting Costimulatory Humabody VH Therapeutic for Treating PSMA-Positive Tumors

Archer S
April 15, 2024
Clin Cancer Res
https://pubmed.ncbi.nlm.nih.gov/38593226

This article is currently being updated. View its version on PubMed.

https://pubmed.ncbi.nlm.nih.gov/38593226

Research summary

This study evaluates the preclinical efficacy and safety of CB307, a trispecific Humabody VH therapeutic targeting PSMA on tumor cells, CD137 on T cells, and HSA for half-life extension, aiming to induce localized T-cell activation in PSMA-expressing tumors.

Key outcome of the study

CB307 induces PSMA-dependent CD137 activation, enhances T-cell proliferation and cytokine production, inhibits tumor growth in PSMA-expressing tumor models, shows synergistic effects with PD-1/PD-L1 inhibitors, and exhibits a favorable safety profile in preclinical studies.

Mouse model

Double-humanized HSA-FcRn transgenic mouse model developed by genOway, expressing human serum albumin (HSA) and human neonatal Fc receptor (hFcRn) to study the pharmacokinetics and therapeutic effects of CB307.

TARGET:
Folh1
PSMA, CD137, 4-1BB

Keywords

Prostate cancer, Immunotherapy, T-cell activation, PSMA-targeted therapy, CD137 agonist, Pharmacokinetics

Technical specifications

Double-humanized HSA-FcRn transgenic mouse, Human FcRn and HSA expression, PSMA/CD137/HSA targeting, In vivo tumor models, T-cell activation assays, Pharmacokinetic analysis

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Catalogue product

genO‑HSA/hFcRn

Double humanized genO‑HSA/hFcRn mouse model as a cutting-edge platform for preclinical development of HSA and FcRn-oriented therapeutics.

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