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🇪🇺EU · EMAAuthorisedATC: A05AA01Orphan Medicine

Chenodeoxycholic acid Leadiant (previously Chenodeoxycholic acid sigma-tau)(chenodeoxycholic acid)

Xanthomatosis, Cerebrotendinous;Metabolism, Inborn Errors

Marketing Authorisation Holder: Leadiant GmbH

EMA Authorisation: 10/04/2017

INN: chenodeoxycholic acid

Indication

Chenodeoxycholic acid is indicated for the treatment of inborn errors of primary bile acid synthesis due to sterol 27 hydroxylase deficiency (presenting as cerebrotendinous xanthomatosis (CTX)) in infants, children and adolescents aged 1 month to 18 years and adults.

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.