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Gunagratinib (ICP-192) is a highly selective, orally active small-molecule pan-FGFR (fibroblast growth factor receptor) inhibitor that irreversibly inhibits FGFR activity by covalent binding. It is designed to overcome resistance to first-generation reversible FGFR inhibitors and demonstrates potent anti-tumor activity in preclinical and clinical studies. Gunagratinib is being developed primarily for the treatment of advanced solid tumors with FGFR gene aberrations, including cholangiocarcinoma and urothelial carcinoma. The drug has shown safety, tolerability, and preliminary efficacy in phase I/II trials for patients with FGF/FGFR gene alterations[1][2][3][4][5][6].
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