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89Zr-Lumi804-anti-LHRH + 177Lu-Lumi804-anti-LHRH

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-LHRH + 177Lu-Lumi804-anti-LHRH is a preclinical radiotheranostic pair developed by Lumiphore for the management of prostate cancer. This matched pair consists of an anti-LHRH monoclonal antibody conjugated to Lumiphore's proprietary Lumi804 macrocyclic chelator, which is an octadentate ligand based on hydroxypyridinone coordinating units. The diagnostic component is labeled with Zirconium-89 (89Zr) for positron emission tomography (PET) imaging, while the therapeutic component is labeled with Lutetium-177 (177Lu) for targeted beta-radiation therapy. Both conjugates target the luteinizing hormone-releasing hormone (LHRH) receptor, which is frequently overexpressed in prostate cancer cells. This theranostic approach allows for personalized treatment by using the imaging agent to identify patients with high target expression and to monitor the distribution and efficacy of the subsequent therapeutic dose.

Other names
Lumi804™-Anti-LHRH (Zr-89 imaging / Lu-177 therapy)Zr-89-Lumi804 anti-LHRHZr89-Lumi804 anti-LHRHZr 89-Lumi804 anti-LHRHLu-177-Lumi804 anti-LHRHLu177-Lumi804 anti-LHRHLu 177-Lumi804 anti-LHRH
02

Targets

GnRHR (Gonadotropin-releasing hormone receptor)

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