Drug intelligence / Profile preview

18F-FXA

Development stage
Unknown
Lead developer
Stanford University
Modality
Alpha Emitters → Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Beta Emitters → Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous
01

Overview

18F-FXA is a radiopharmaceutical positron emission tomography (PET) tracer specifically designed for the non-invasive imaging of activated Factor X (Factor Xa), a key enzyme in the blood coagulation cascade. Developed primarily by researchers at Stanford University, the tracer is a small molecule derivative of a Factor Xa inhibitor labeled with the radioactive isotope fluorine-18. By binding with high affinity to the catalytic active site of Factor Xa, which is highly concentrated at the surface of active thrombi, 18F-FXA allows for the precise localization and visualization of acute thromboembolic events such as deep vein thrombosis (DVT) and pulmonary embolism (PE). This functional imaging approach potentially offers a significant advantage over traditional anatomical imaging (like ultrasound or CT) by distinguishing active, growing clots from older, stable, or organized fibrin deposits, thereby assisting in the diagnosis and management of acute thrombosis.

Other names
Fluorine-18 Factor Xa tracerFluorine18 Factor Xa tracerFluorine 18 Factor Xa tracer18F-labeled Factor Xa inhibitor18F-labeled activated Factor X ligand
02

Targets

F10 (Factor Xa)

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