MedPath
EMA Product

Jetrea

Product approved by European Medicines Agency (EU)

Basic Information

Jetrea

Regulatory Information

EMEA/H/C/002381

Authorised

March 13, 2013

January 17, 2013

15

January 16, 2021

Company Information

Sweden

Gustavslundsv. 143 16751 Bromma

Inceptua Ab

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Jetrea is indicated in adults for the treatment of vitreomacular traction (VMT), including when associated with macular hole of diameter less than or equal to 400 microns.

Overview Summary

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

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