Mon-Fri 9:00-18:00 CET+39 095 7211344info@vitasanlabs.com

Family · Pharmaceutical analytical standards

Erdafitinib

An oral FGFR inhibitor, approved in the United States in 2019 (under accelerated approval, made full in 2024) and in Europe in 2024 for advanced urothelial carcinoma with FGFR3 gene alterations. This family brings together the active ingredient, nitrosamines and other impurities.

Did you know?The FDA regarded it as a 'first-in-class' medicine, and it was approved together with a 'companion' genetic test that looks for FGFR3 or FGFR2 alterations in the tumour.

ErdafitinibGo to the active ingredient →
ErdafitinibActive ingredientErdafitinibCat. No. P-E078-001CAS 1346242-81-6

Need a molecule you cannot find?

Custom synthesis of impurities, metabolites and labelled compounds, with the same characterisation level.