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Avonex (INTERFERON BETA-1A)
Avonex works by binding to the interferon alpha/beta receptor, which helps to reduce inflammation and slow disease progression in multiple sclerosis.
Avonex (Interferon Beta-1a) is a medication originally developed by Biogen and currently owned by the same company. It is a recombinant form of interferon beta-1a, a protein that targets the interferon alpha/beta receptor, and is classified as an interferon beta. Avonex is FDA-approved for the treatment of relapsing-remitting multiple sclerosis, and has been commercially available since 1996. As a branded medication, it is not yet available as a generic. Key safety considerations include potential flu-like symptoms, injection site reactions, and liver enzyme elevations.
At a glance
| Generic name | INTERFERON BETA-1A |
|---|---|
| Sponsor | Biogen |
| Drug class | Interferon beta [EPC] |
| Target | Interferon alpha/beta receptor |
| Modality | Recombinant protein |
| Therapeutic area | Neuroscience |
| Phase | FDA-approved |
| First approval | 1996 |
| Annual revenue | 800 |
Mechanism of action
The mechanism(s) by which REBIF (interferon beta-1a) exerts its therapeutic effects in patients with multiple sclerosis is unknown.
Approved indications
- Relapsing remitting multiple sclerosis
Common side effects
- Influenza-like symptoms
- Influenza-like symptoms
- Headache
- Headache
- Fatigue
- Fatigue
- Fever
- Fever
- Rigors
- Rigors
- Chest pain
- Chest pain
Key clinical trials
- An Observational Study to Learn About the Interferon-beta Exposure of Pregnant Women During the Second and Third Trimester in Finland and Sweden
- Open Label Randomized Multicenter to Assess Efficacy & Tolerability of Ofatumumab 20mg vs. First Line DMT in RMS (PHASE3)
- Safety and Efficacy of Fingolimod in Pediatric Patients With Multiple Sclerosis (PHASE3)
- A Study to Learn More About The Safety of Diroximel Fumarate (VUMERITY®) in Participants Who Took it During Pregnancy And About the Health of Their Babies
- Traditional Versus Early Aggressive Therapy for Multiple Sclerosis Trial (NA)
- A Study to Evaluate the Safety, Tolerability, and Efficacy of BIIB017 (Peginterferon Beta-1a) in Pediatric Participants for the Treatment of Relapsing-Remitting Multiple Sclerosis (PHASE3)
- Determining the Effectiveness of earLy Intensive Versus Escalation Approaches for RRMS (PHASE4)
- Pregnancy Exposure Registry for Vumerity (Diroximel Fumarate)
Patents
| Patent | Expiry | Type |
|---|---|---|
| Biologic Exclusivity |
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| FDA label | Mechanism, indications, dosing, boxed warnings, drug interactions |
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
| FDA Orange Book | Patents + exclusivity |
| SEC EDGAR | Revenue + earnings |