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Lutetium-177-dotaga-iac is an investigational radiopharmaceutical designed for targeted radionuclide therapy of tumors expressing the αvβ3 integrin, which is associated with angiogenesis. The compound consists of the radioactive isotope lutetium-177 chelated to DOTAGA-IAC, a molecule that targets αvβ3 integrin on tumor cells. Upon binding to its target, the radiolabeled agent delivers localized beta radiation to tumor tissue, causing cellular damage and death while sparing most normal tissues. Preclinical studies have demonstrated high radiolabeling yield and rapid clearance from non-target tissues. Clinical trials are ongoing in patients with unresectable angiogenic breast cancer as a second or third-line treatment[2][4][5].
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