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177Lu-HER3 ARC is a preclinical-stage antibody radioconjugate (ARC) being developed through a collaboration between Actinium Pharmaceuticals and AVEO Oncology (a subsidiary of LG Chem). The therapeutic candidate comprises the anti-HER3 monoclonal antibody AT-02, conjugated to the beta-emitting radionuclide Lutetium-177 (177Lu) using a p-SCN-Bn-DOTA chelator. It specifically targets the HER3 (ErbB3) receptor, a member of the epidermal growth factor receptor (EGFR) family that is frequently overexpressed in various solid malignancies, including ovarian, colorectal, prostate, and renal cancers. HER3 overexpression is often linked to poor prognosis and resistance to existing therapies. By binding to HER3 on the surface of cancer cells, 177Lu-HER3 ARC delivers localized, high-energy radiation that induces DNA damage and subsequent apoptosis. Preclinical studies have demonstrated significant reductions in tumor burden in HER3-expressing models compared to standard treatments.
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