Family · Pharmaceutical analytical standards
Elexacaftor
A CFTR protein corrector used in cystic fibrosis in a triple combination with tezacaftor and ivacaftor. It was approved in the United States in October 2019 for patients aged 12 and over with at least one copy of the F508del mutation. This family brings together the active ingredient, metabolites, labelled standards, nitrosamines and other impurities.
Did you know?A single copy of the F508del mutation is enough to use it: with its arrival it was estimated that about 90% of people with cystic fibrosis could receive an effective targeted therapy.
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Custom synthesis of impurities, metabolites and labelled compounds, with the same characterisation level.
