Drug intelligence / Profile preview

18F-TATE

Development stage
Unknown
Lead developer
Chinese PLA General Hospital
Modality
Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Peptides
Administration
Intravenous
01

Overview

18F-TATE is a radiolabeled somatostatin analog developed for the diagnostic imaging of neuroendocrine tumors (NETs) using positron emission tomography (PET). It typically comprises the somatostatin receptor-targeting peptide [Tyr3]octreotate (TATE) conjugated to a chelating agent like NOTA, which is then labeled with the radioisotope fluorine-18, often utilizing the aluminum fluoride ([Al18F]2+) complexation method. The tracer specifically targets somatostatin receptors (primarily SSTR2), which are highly expressed on the surface of NET cells. 18F-TATE is designed to overcome the logistical limitations of 68Ga-labeled tracers, such as 68Ga-DOTATATE, by leveraging the longer half-life (110 minutes) and superior imaging characteristics of fluorine-18, enabling centralized production and potentially higher-resolution imaging.

Other names
[18F]AlF-NOTA-octreotate18F-AlF-NOTA-DOTATATE18F-AlF-NOTA-TATE18F-labeled somatostatin analog
02

Targets

SSTR2 (Somatostatin receptor type 2)SSTR3 (Somatostatin receptor 3)SSTR5 (Somatostatin receptor 5)

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