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EMA Product

Verkazia

Product approved by European Medicines Agency (EU)

Basic Information

Verkazia

Regulatory Information

EMEA/H/C/004411

Authorised

July 6, 2018

July 20, 2017

7

April 25, 2023

Company Information

Finland

Niittyhaankatu 20 33720 Tampere

Santen Oy

Drug Classification

Orphan MedicineAccelerated Assessment

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Treatment of severe vernal keratoconjunctivitis (VKC) in children from 4 years of age and adolescents.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Verkazia. It explains how the Agency assessed the medicine to recommend its authorisation in the EU and its conditions of use. It is not intended to provide practical advice on how to use Verkazia. For practical information about using Verkazia, patients should read the package leaflet or contact their doctor or pharmacist.

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