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🇪🇺EU · EMAAuthorisedATC: A16AB20

Elfabrio(pegunigalsidase alfa)

Fabry Disease

Marketing Authorisation Holder: Chiesi Farmaceutici S.p.A

EMA Authorisation: 04/05/2023

INN: pegunigalsidase alfa

Indication

Elfabrio is indicated for long-term enzyme replacement therapy in adult patients with a confirmed diagnosis of Fabry disease (deficiency of alpha-galactosidase).

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.