Drug intelligence / Profile preview

CD69-targeted PET tracer

Development stage
Preclinical
Lead developer
Peking University Cancer Hospital & Institute
Modality
Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

CD69-targeted PET tracers are a class of diagnostic radiopharmaceuticals designed for non-invasive, real-time imaging of T-cell activation and immune responses in the tumor microenvironment. CD69 is an early activation marker of T cells, making it a highly sensitive biomarker for monitoring early immune activation following immunotherapy (such as immune checkpoint inhibitors). Preclinical candidates, such as the zirconium-89 labeled monoclonal antibody tracer 89Zr-DFO-CD69-Mb-7 (developed by researchers at Tongji Hospital, Huazhong University of Science and Technology, and Beijing Cancer Hospital) and 89Zr-DFO-anti-CD69 (developed at the University of Pittsburgh), have demonstrated high affinity and specificity for CD69. These tracers enable longitudinal PET/CT imaging to visualize tumor-infiltrating activated T cells, allowing for early prediction of treatment response and differentiation between effective and ineffective immunotherapy regimens before changes in tumor size occur.

Other names
CD69 immuno-PET tracerCD-69 immuno-PET tracerCD 69 immuno-PET tracerCD69-targeted PET probeCD-69-targeted PET probeCD 69-targeted PET probeCD69-targeted radiotracerCD-69-targeted radiotracerCD 69-targeted radiotracer
02

Targets

CD69 (CD69 molecule)

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