Drug intelligence / Profile preview

Pb-212-RMX-VH

Development stage
Preclinical
Lead developer
Radiomedix
Modality
Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Peptides
Administration
Intravenous
01

Overview

Pb-212-RMX-VH (also known as 212Pb-RMX-VH or 212Pb-RMX-VH-PKM in its second-generation formulation) is an investigational targeted alpha therapy (TAT) radiopharmaceutical being co-developed by RadioMedix and Vect-Horus. It consists of a peptide vector (RMX-VH) designed to target the Low-Density Lipoprotein Receptor (LDLR), which is highly overexpressed in various solid tumors, conjugated to the alpha-emitting radioisotope lead-212 (Pb-212) via a DOTAM chelator. By binding to LDLR, the radioconjugate is internalized into cancer cells, where the decay of Pb-212 delivers high-energy, short-range alpha radiation that induces lethal DNA double-strand breaks. Pb-212-RMX-VH is currently in preclinical development (Pharma/Tox stage) for the treatment of glioblastoma (GBM) and pancreatic ductal adenocarcinoma (PDAC), supported by companion diagnostic imaging agents such as 203Pb-RMX-VH-PIB.

Other names
212Pb-RMX-VH-PKM212Pb-labeled LDLR-targeting peptidelead-212 RMX-VHlead212 RMX-VHlead 212 RMX-VH
02

Targets

LDLR (Low-density lipoprotein receptor)DNA

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