Plegridy

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peginterferon beta-1a

Authorised
This medicine is authorised for use in the European Union.

Overview

Plegridy is a medicine used to treat multiple sclerosis (MS), a disease in which inflammation damages the protective insulation around nerves (demyelination) as well as the nerves themselves. It is used specifically in adults with a type of MS known as relapsing-remitting MS, where the patient has flare-ups of symptoms (relapses) between periods of recovery (remissions).

Plegridy contains the active substance peginterferon beta-1a.

This EPAR was last updated on 20/12/2019

Authorisation details

Product details
Name
Plegridy
Agency product number
EMEA/H/C/002827
Active substance
peginterferon beta-1a
International non-proprietary name (INN) or common name
peginterferon beta-1a
Therapeutic area (MeSH)
Multiple Sclerosis
Anatomical therapeutic chemical (ATC) code
L03AB13
Publication details
Marketing-authorisation holder
Biogen Netherlands B.V.
Revision
18
Date of issue of marketing authorisation valid throughout the European Union
17/07/2014
Contact address

Prins Mauritslaan 13
1171 LP Badhoevedorp
The Netherlands

Product information

19/09/2019 Plegridy - EMEA/H/C/002827 - II/0052/G

Contents

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Pharmacotherapeutic group

Immunostimulants

Therapeutic indication

Treatment of relapsing remitting multiple sclerosis in adult patients.

Assessment history

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