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IR199 is a radiopharmaceutical targeting Claudin 18.2 (CLDN18.2), a tight junction protein frequently overexpressed in gastric and pancreatic adenocarcinomas. It is being developed as a theranostic agent, utilizing Gallium-68 ([68Ga]) for positron emission tomography (PET) imaging to assess biodistribution and tumor uptake, and Iodine-131 ([131I]) for dosimetry and potentially targeted radionuclide therapy. The agent is currently in early-phase clinical trials to evaluate its safety and imaging characteristics in patients with CLDN18.2-positive gastrointestinal cancers.
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