Drug intelligence / Profile preview

89Zr-Lumi804-Anti-PSMA + 227Th-Lumi804-Anti-PSMA

Development stage
Preclinical
Lead developer
Lumiphore
Modality
Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

89Zr-Lumi804-Anti-PSMA + 227Th-Lumi804-Anti-PSMA is a preclinical radiotheranostic pair developed by Lumiphore for the imaging and treatment of prostate cancer. The system utilizes an anti-prostate-specific membrane antigen (PSMA) monoclonal antibody conjugated to Lumiphore's proprietary Lumi804 macrocyclic bifunctional chelator. The Lumi804 chelator is an octadentate ligand based on 1-hydroxypyridin-2-one (HOPO) units, designed to stably bind various radiometals at room temperature. In this matched pair, the antibody is labeled with Zirconium-89 (89Zr) for positron emission tomography (PET) imaging to identify and localize PSMA-expressing tumors, and with Thorium-227 (227Th) for targeted alpha therapy (TAT) to deliver high-energy alpha radiation directly to the cancer cells. This approach allows for personalized medicine by using the same targeting vector for both diagnostic imaging and therapeutic intervention.

Other names
89Zr-Lumi804-Anti-PSMA + Th-227-Lumi804-Anti-PSMA-Lumiphore-PSMA-radiopharmaceutical-Zr-89 PET imaging agent-Th-227 targeted alpha therapeutic-radiotheranostic pair-radioimmunoconjugate-prostate cancer (imaging & therapy)Zr-89-Lumi804 anti-PSMAZr89-Lumi804 anti-PSMAZr 89-Lumi804 anti-PSMATh-227-Lumi804 anti-PSMATh227-Lumi804 anti-PSMATh 227-Lumi804 anti-PSMALumi804-Anti-PSMA (Zr-89 imaging / Th-227 therapy)
02

Targets

PSMA (Prostate-specific membrane antigen)

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