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EMA Product

Avonex

Product approved by European Medicines Agency (EU)

Basic Information

Avonex

Regulatory Information

EMEA/H/C/000102

Authorised

March 13, 1997

39

April 10, 2025

Company Information

the netherlands

Prins Mauritslaan 13 1171 LP Badhoevedorp

Biogen Netherlands BV

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Avonex is indicated for the treatment of: - patients diagnosed with relapsing multiple sclerosis (MS). In clinical trials, this was characterised by two or more acute exacerbations (relapses) in the previous three years without evidence of continuous progression between relapses; Avonex slows the progression of disability and decreases the frequency of relapses; - patients with a single demyelinating event with an active inflammatory process, if it is severe enough to warrant treatment with intravenous corticosteroids, if alternative diagnoses have been excluded, and if they are determined to be at high risk of developing clinically definite MS. Avonex should be discontinued in patients who develop progressive MS.

Overview Summary

Avonex is a medicine used to treat: - patients with relapsing multiple sclerosis (MS). MS is a disease in which inflammation damages the protective insulation around nerves (demyelination) as well as the nerves themselves. In relapsing MS, the patient has attacks (relapses) between periods with no symptoms. Avonex slows the progression of disability and reduces the number of relapses; - patients who have had a single attack of demyelination, when this is severe enough to need treatment with injectable corticosteroids (anti‑inflammatory medicines). It is used when the patient is considered to be at high risk of developing MS. Before using Avonex, doctors need to exclude other causes for the symptoms. Avonex contains the active substance interferon beta-1a.

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