Prognia
Drug Database
🇪🇺EU · EMAAuthorisedATC: L04AL03

Imaavy(nipocalimab)

Myasthenia Gravis

Marketing Authorisation Holder: Janssen Cilag International NV

EMA Authorisation: 28/11/2025

INN: nipocalimab

Indication

Imaavy is indicated as an add-on to standard therapy for the treatment of generalised myasthenia gravis (gMG) in adult and adolescent patients aged 12 years of age and older who are anti‑acetylcholine receptor (AChR) or anti-muscle-specific tyrosine kinase (MuSK) antibody positive.

Official EMA Resources

View on EMA (ema.europa.eu)

AI Drug & Interaction Analysis

Free account required

Ask Prognia AI about Imaavy — 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.