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68Ga-WL12

Development stage
Unknown
Lead developer
Johns Hopkins University
Modality
Small Molecules, Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Peptides
Administration
Intravenous
01

Overview

68Ga-WL12 is a peptide-based radiopharmaceutical designed for positron emission tomography (PET) imaging of programmed cell death ligand-1 (PD-L1) expression in tumors. The compound consists of the WL12 peptide, which binds specifically to PD-L1, conjugated with a chelator (such as NOTA or DOTAGA) and radiolabeled with gallium-68. This agent enables noninvasive quantification and visualization of PD-L1 expression in vivo, supporting patient selection and monitoring for immunotherapies targeting the PD-1/PD-L1 axis. Preclinical studies demonstrated high affinity for PD-L1 and favorable pharmacokinetics; first-in-human trials have shown safety, feasibility, and correlation between tracer uptake and tumor PD-L1 levels in patients with advanced non–small cell lung cancer[3][4][5][7].

Other names
gallium Ga 68-WL12
02

Targets

CD274 (Programmed cell death protein 1 ligand 1)

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