Drug intelligence / Profile preview

[89Zr]Zr-DFO-emapalumab

Development stage
Phase 1
Lead developer
Barbara Ann Karmanos Cancer Institute
Modality
Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Positron Emitters → Radiopharmaceuticals, Gamma Emitters → Radiopharmaceuticals, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

[89Zr]Zr-DFO-emapalumab is a radiolabeled monoclonal antibody-based diagnostic agent designed for immunoPET imaging. It consists of emapalumab, an anti-interferon gamma (IFNγ) monoclonal antibody, conjugated to the chelator DFO and labeled with the positron emitter zirconium-89 ([^89Zr]). The drug targets IFNγ, a cytokine involved in immune responses and inflammation. Its primary mechanism is binding to IFNγ, enabling non-invasive PET imaging of IFNγ expression in vivo. This allows assessment of immune activity within tumors or inflammatory lesions and monitoring response to immunotherapies such as immune checkpoint inhibitors. The agent is under clinical investigation primarily for use in oncology (notably non-small cell lung cancer) and potentially other diseases characterized by altered IFNγ activity[1][2][3].

Other names
[89Zr]Zr-DFO-emapalumabZirconium Zr 89-DFO-emapalumab
02

Targets

IFNG (Interferon gamma)

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