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EMA Product

Yargesa

Product approved by European Medicines Agency (EU)

Basic Information

Yargesa

Regulatory Information

EMEA/H/C/004016

Authorised

March 22, 2017

January 26, 2017

5

February 29, 2024

Company Information

netehrlands

Rouboslaan 32 2252 TR Voorschoten

Piramal Critical Care BV

Drug Classification

Generic Medicine

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Yargesa is indicated for the oral treatment of adult patients with mild to moderate type 1 Gaucher disease. Yargesa may be used only in the treatment of patients for whom enzyme replacement therapy is unsuitable. Yargesa is indicated for the treatment of progressive neurological manifestations in adult patients and paediatric patients with Niemann-Pick type C disease.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Yargesa. 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 Yargesa. For practical information about using Yargesa, patients should read the package leaflet or contact their doctor or pharmacist.

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