The treating physician/investigator contacts Lilly when, based on their medical opinion, a patient meets the criteria for inclusion in the expanded access program.
Have metastatic urothelial carcinoma (UC) or other solid tumor with a qualifying fibroblast growth factor receptor 3 (FGFR3) genetic alteration.
Have exhausted other approved treatments, including erdafitinib for UC.
Are not eligible for an ongoing vepugratinib clinical trial
Currently enrolled in an ongoing clinical study of vepugratinib
Have a known severe (greater than or equal to (≥) Grade 3) hypersensitivity to any component or excipient of vepugratinib.
Current evidence of corneal keratopathy or retinal disorder confirmed by ocular examination. Exception: Individuals with asymptomatic ophthalmic conditions assessed by the investigator to pose minimal risk.
Are pregnant, breastfeeding, or intent to become pregnant during the study or within 6 months of the last dose of study intervention.
Vepugratinib
DrugAdministered orally
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