Drug intelligence / Profile preview

[18F]fluorobenzoyl-doxorubicin

Development stage
Preclinical
Lead developer
University of California, San Francisco
Modality
Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Positron Emitters → Radiopharmaceuticals, Small Molecules
Administration
Intra-arterial, Intravenous
01

Overview

[18F]fluorobenzoyl-doxorubicin (also known as [18F]FB-Dox) is a fluorine-18 radiolabeled analog of the chemotherapeutic drug doxorubicin. Developed by researchers at the University of California, San Francisco (UCSF), it serves as a positron emission tomography (PET) imaging tracer and diagnostic tool. It is primarily used to evaluate the binding efficiency of endovascular ChemoFilter devices designed to capture excess chemotherapeutics during intra-arterial chemotherapy (such as for hepatocellular carcinoma) and to assess the in vivo biodistribution and pharmacokinetics of doxorubicin (e.g., following blood-brain barrier disruption or during hepatic intra-arterial chemotherapy).

Other names
[18F]FB-DOX[18F]fluorobenzoyl doxorubicin18F-FB-Dox18F-fluorobenzoyl-doxorubicindoxorubicin-[18F]fluorobenzamidefluorine-18 fluorobenzoyl-doxorubicinfluorine18 fluorobenzoyl-doxorubicinfluorine 18 fluorobenzoyl-doxorubicin
02

Targets

DNATOP2A (DNA topoisomerase II)TOP2B (DNA topoisomerase II beta)

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