Prognia
Drug Database
🇪🇺EU · EMAAuthorisedATC: L04ACOrphan Medicine

Enspryng(satralizumab)

Neuromyelitis Optica

Marketing Authorisation Holder: Roche Registration GmbH

EMA Authorisation: 24/06/2021

INN: satralizumab

Indication

Satralizumab (Enspryng) is indicated as a monotherapy or in combination with immunosuppressive therapy (IST) for the treatment of neuromyelitis optica spectrum disorders (NMOSD) in adult and adolescent patients from 12 years of age who are anti-aquaporin-4 IgG (AQP4-IgG) seropositive.

Official EMA Resources

View on EMA (ema.europa.eu)

AI Drug & Interaction Analysis

Free account required

Ask Prognia AI about Enspryng — dosing recommendations, drug interactions, and current guideline evidence from ESC, EMA, NICE and more.

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