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**BGP-31172** is a highly potent and selective covalent inhibitor targeting FGFR3, demonstrating promising antitumor activity in patients with FGFR3-altered metastatic urothelial carcinoma (mUC), including those previously treated with FGFR inhibitors. In early clinical data, it was well-tolerated at 200 mg BID, with low rates of common FGFRi-related treatment-emergent adverse events (TEAEs) such as palmar-plantar erythrodysesthesia (PPE, 7%), onycholysis (0%), and retinopathy (0%). Non-clinical toxicology studies in rats and dogs over 28 days supported its safety profile, positioning it as a potential next-generation therapy for FGFR-driven cancers.
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