Drug intelligence / Profile preview

89Zr-DOTATOC

Development stage
Preclinical
Lead developer
Kyoto University
Modality
Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Positron Emitters → Radiopharmaceuticals, Gamma Emitters → Radiopharmaceuticals, Peptides
Administration
Intravenous
01

Overview

89Zr-DOTATOC is a zirconium-89-labeled DOTA-octreotide conjugate developed as a positron emission tomography (PET) imaging radiopharmaceutical. It targets the somatostatin receptor (SSTR), which is highly expressed in neuroendocrine tumors. By utilizing zirconium-89, a PET radionuclide with a relatively long half-life of approximately 78 hours, the tracer allows for flexible delivery and delayed imaging of SSTR-positive tumors. Preclinical studies, including those conducted at Kyoto University, have optimized its synthesis using an acetate buffer at pH 5.5 to achieve high radiochemical yields without requiring post-labeling purification, demonstrating specific tumor targeting in vitro and in vivo.

Other names
89Zr-DOTA-octreotide89Zr-edotreotidezirconium-89 DOTA-octreotidezirconium89 DOTA-octreotidezirconium 89 DOTA-octreotidezirconium-89-labeled DOTA-octreotidezirconium89-labeled DOTA-octreotidezirconium 89-labeled DOTA-octreotidezirconium-89-labeled edotreotidezirconium89-labeled edotreotidezirconium 89-labeled edotreotide
02

Targets

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

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