Prognia
Drug Database
🇪🇺EU · EMAAuthorisedATC: L04

Briumvi(ublituximab)

Multiple Sclerosis, Relapsing-Remitting;Multiple Sclerosis

Marketing Authorisation Holder: Neuraxpharm Pharmaceuticals S.L.

EMA Authorisation: 31/05/2023

INN: ublituximab

Indication

Briumvi is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (RMS) with active disease defined by clinical or imaging features.

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.