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Betaferon

EU: Approved in the EU since 1995US: FDA approved 1993

Molecule type
Protein
Mechanism (ChEMBL)
Interferon alpha/beta receptor agonist
Targets
Interferon alpha/beta receptor
Availability
Authorised in all EU and EEA countries. Reimbursement is decided by each country.

Approvals

  • USBetaseron · Approved1993-07-23 Source
  • EU/EEABetaferon · Authorised1995-11-30 Source
  • EU/EEAExtavia · Withdrawn2008-05-20 Source

Other regulatory events

  • Withdrawn · Extavia2025-04-25 Source

Safety communications

None recorded.

Most-reported side effects (FDA reports)

Reports to the FDA's adverse event system (FAERS) show what people and doctors reported while taking the medicine. They do not prove the medicine caused it, and they are not rates.

19,777 reports in total, 11,313 marked serious.

  • Influenza like illness1,427
  • Multiple sclerosis relapse1,420
  • Fatigue1,232
  • Injection site pain1,217
  • Multiple sclerosis1,203
  • Drug ineffective996
  • Injection site erythema993
  • Pain884
  • Headache880
  • Injection site reaction852

Trials

Key trials

Large trials with a reported result on their main goal.

Running now

  • TWINS

    Not yet recruiting · Phase 3 · Relapsing MS · ongoing

  • INFORM

    Running, not recruiting · MS (type not specified) · ongoing

  • STOP-I-SEP

    Running, not recruiting · Phase 3 · Progressive MS · ongoing

  • DELIVER-MS

    Running, not recruiting · Phase 4 · Relapsing MS · ongoing

  • ABIRISK

    Ongoing · Phase 4 · MS (type not specified) · ongoing

  • VITAD-2010

    Ongoing · Phase 2 · Relapsing and progressive · ongoing

Other trials (56)

Completed small trials, dose-finding studies and trials in other diseases.

For information only, not medical advice. Talk to your neurologist before changing treatment.

Hypotheses involving this medicine

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Lab studies

Lab studies in animals or cells. Results in animals often do not hold in people, and these studies never change the status of an idea.

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