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Fluorine F 18 + GEH121224 is a radioconjugate composed of GEH121224, a ligand that specifically targets human epidermal growth factor receptor 2 (HER2; also known as ErbB2), and is labeled with the positron-emitting radioisotope fluorine F 18. The compound is designed for use as a positron emission tomography (PET) radiotracer for non-invasive imaging of HER2 expression in patients, primarily with advanced or metastatic HER2-positive breast cancer. The radiotracer allows clinicians to assess HER2 positivity and tumor burden, aiding in diagnosis and therapy planning. The use of the F 18 isotope allows for high-resolution PET imaging to detect and quantify HER2 status in real time[7][1][2][3]. Currently, the drug is in early-stage clinical trials to evaluate its safety, radiation dosimetry, biodistribution, pharmacokinetics, and optimal imaging protocols in the indicated patient population[2][3][8].
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