A Post-Authorization Safety Study of Interferon Beta Therapy in Participants With Multiple Sclerosis

CompletedOBSERVATIONAL
Enrollment

626

Participants

Timeline

Start Date

November 27, 2017

Primary Completion Date

July 31, 2019

Study Completion Date

July 31, 2019

Conditions
Multiple Sclerosis, Relapsing-Remitting
Interventions
DRUG

SC Peginterferon beta-1a

All participants will be treated with their current SC interferon beta medication according to the Fachinformation (German equivalent to summary of product characteristics \[SmPC\]).

DRUG

SC interferon beta-1a

All participants will be treated with their current SC interferon beta medication according to the Fachinformation (German equivalent to summary of product characteristics \[SmPC\]).

DRUG

SC interferon beta-1b

All participants will be treated with their current SC interferon beta medication according to the Fachinformation (German equivalent to summary of product.

Trial Locations (1)

37073

Research Site, Göttingen

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

AMS Advanced Medical Services GmbH

INDUSTRY

lead

Biogen

INDUSTRY

NCT03347370 - A Post-Authorization Safety Study of Interferon Beta Therapy in Participants With Multiple Sclerosis | Biotech Hunter | Biotech Hunter