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89Zr-DFO-nimotuzumab

Development stage
Phase 2
Lead developer
University of Saskatchewan
Modality
Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

**89Zr-DFO-nimotuzumab** is an investigational EGFR-targeted immunoPET imaging agent. It consists of the humanized anti-EGFR monoclonal antibody nimotuzumab conjugated to the desferrioxamine chelator and radiolabeled with the positron-emitting isotope zirconium-89. Following intravenous administration, it is intended to bind EGFR-expressing tumor cells and enable noninvasive PET/CT visualization and measurement of tumor EGFR expression, potentially supporting selection of patients for EGFR-directed therapy. The University of Saskatchewan-sponsored clinical study NCT04235114 is evaluating the tracer in lung and colorectal cancers. ([clinicaltrials.gov](https://clinicaltrials.gov/study/NCT04235114))

Other names
[89Zr]Zr-DFO-nimotuzumab89Zr-nimotuzumab
02

Targets

EGFR T790M (Epidermal growth factor receptor T790M mutant)

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