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🇪🇺EU · EMAAuthorisedATC: L04AJ01

Bekemv(Eculizumab)

Hemoglobinuria, Paroxysmal

Marketing Authorisation Holder: Amgen Technology (Ireland) UC

EMA Authorisation: 19/04/2023

INN: eculizumab

Indication

Bekemv is indicated in adults and children for the treatment of paroxysmal nocturnal haemoglobinuria (PNH). Evidence of clinical benefit is demonstrated in patients with haemolysis with clinical symptom(s) indicative of high disease activity, regardless of transfusion history (see section 5.1).

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.