Drug intelligence / Profile preview

[18F]fluorocellobiose

Development stage
Unknown
Lead developer
NIH Clinical Center
Modality
Small Molecules, Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

[18F]fluorocellobiose (also known as [18F]FCB) is a novel investigational positron emission tomography (PET) radiopharmaceutical developed by the National Institutes of Health (NIH) Clinical Center. It is a fluorine-18-labeled derivative of cellobiose, a disaccharide, and is synthesized from commercial [18F]FDG (fluorodeoxyglucose). The tracer's mechanism of action targets the enzyme beta-glucosidase (BGL), which is expressed by several filamentous fungi, including Aspergillus fumigatus. Upon encountering BGL-producing fungi, [18F]FCB is metabolized into [18F]FDG and glucose; the resulting [18F]FDG is then trapped within the metabolically active fungal cells, enabling specific PET imaging of fungal infections. It is currently being investigated in Phase 1 clinical trials for the detection and monitoring of invasive fungal infections (IFIs), particularly invasive mold infections such as invasive aspergillosis, and for evaluating antifungal treatment response.

Other names
[18F]fluorocellobiose2-deoxy-2-[18F]fluorocellobiose
02

Targets

BGL (beta-Glucosidase)

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