Drug intelligence / Profile preview

[68Ga]Ga-DOTA-RET-L7

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

Overview

[68Ga]Ga-DOTA-RET-L7 is a preclinical, research-stage radiopharmaceutical developed as a positron emission tomography (PET) imaging agent. It consists of the RET-L7 peptide, which was discovered via phage display and selected for its high-affinity binding to the receptor tyrosine kinase RET, conjugated to the chelator DOTA and radiolabeled with gallium-68 (68Ga). RET is highly overexpressed in neuroendocrine prostate cancer (NEPC), an aggressive, treatment-resistant subtype that is frequently prostate-specific membrane antigen (PSMA)-low or PSMA-negative. In preclinical mouse xenograft models, [68Ga]Ga-DOTA-RET-L7 demonstrated high, specific tumor uptake in RET-positive NEPC tumors with rapid blood clearance and strong self-blockade. It forms a theranostic pair with its therapeutic partner, [177Lu]Lu-DOTA-RET-L7, offering a promising diagnostic and therapeutic approach for PSMA-negative prostate cancer.

Other names
68Ga-DOTA-RET-L7Ga-68-DOTA-RET-L7Ga68-DOTA-RET-L7Ga 68-DOTA-RET-L7Gallium-68 DOTA-RET-L7Gallium68 DOTA-RET-L7Gallium 68 DOTA-RET-L7
02

Targets

RET (Rearranged during transfection receptor tyrosine kinase)

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