Drug intelligence / Profile preview

[18F]F-PDL1-3

Development stage
Phase 2
Lead developer
Peking University Cancer Hospital & Institute
Modality
Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Positron Emitters → Radiopharmaceuticals, Peptides
Administration
Intravenous
01

Overview

[18F]F-PDL1-3 is an investigational fluorine-18 (18F)-labeled radionuclide molecular probe designed as a positron emission tomography (PET) imaging agent. It is based on the de novo-designed miniprotein PD-L1-3, which binds to programmed death-ligand 1 (PD-L1) with ultra-high affinity. Developed by Peking University Cancer Hospital & Institute in collaboration with PLA General Hospital, the probe is used to non-invasively detect, quantify, and monitor PD-L1 expression heterogeneity in primary and metastatic lesions in patients with solid tumors, including non-small cell lung cancer (NSCLC), cervical squamous cell cancer, melanoma, breast cancer, and gastrointestinal cancers.

02

Targets

CD274 (Programmed cell death protein 1 ligand 1)

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