Drug intelligence / Profile preview

[18F]-d4-FET

Development stage
Unknown
Lead developer
First Affiliated Hospital of Jinan University
Modality
Small Molecules, Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

[18F]-d4-FET is a deuterated analog of the O-(2-[18F]fluoroethyl)-L-tyrosine ([18F]FET) positron emission tomography (PET) tracer. It is specifically designed to improve metabolic stability by incorporating four deuterium atoms into the fluoroethyl side chain, which reduces in vivo defluorination compared to standard [18F]FET. The tracer acts as a substrate for the large neutral amino acid transporter 1 (LAT1), which is significantly overexpressed in various malignancies, particularly gliomas. By measuring amino acid transport rather than glucose metabolism, [18F]-d4-FET provides superior contrast for brain tumor imaging, aiding in tumor localization, staging, surgical and radiotherapy guidance, and the differentiation of tumor recurrence from radiation-induced changes. It is currently being evaluated in clinical studies by The First Affiliated Hospital of Jinan University for the diagnosis and management of glioma.

Other names
O-(2-[18F]fluoroethyl)-L-tyrosine-d4deuterated [18F]FET[18F]d4-FET
02

Targets

LAT2 (Linker for activation of T cells family member 2)SLC7A5 (Large neutral amino acid transporter small subunit 1)

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