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EMA Product

Ongentys

Product approved by European Medicines Agency (EU)

Basic Information

Ongentys

Regulatory Information

EMEA/H/C/002790

Authorised

June 24, 2016

April 28, 2016

10

September 18, 2024

Company Information

Portugal

Av. da Siderurgia Nacional S. Mamede do Coronado 4745-457

BIAL - PORTELA & CA., S.A.

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Ongentys is indicated as adjunctive therapy to preparations of levodopa/ DOPA decarboxylase inhibitors (DDCI) in adult patients with Parkinson’s disease and end-of-dose motor fluctuations who cannot be stabilised on those combinations.Ongentys is indicated as adjunctive therapy to preparations of levodopa/ DOPA decarboxylase inhibitors (DDCI) in adult patients with Parkinson’s disease and end-of-dose motor fluctuations who cannot be stabilised on those combinations.

Overview Summary

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

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