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Plegridy

EU: Approved in the EU since 2014US: FDA approved 2014

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

  • EU/EEAPlegridy · Authorised18 July 2014 Source
  • USPlegridy · Approved15 August 2014 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.

70 reports in total, 62 marked serious.

  • Multiple sclerosis relapse22
  • Dizziness10
  • Nausea10
  • Drug ineffective7
  • Off label use7
  • Anaemia6
  • General physical health deterioration6
  • Menorrhagia5
  • Drug ineffective for unapproved indication4
  • Therapy non-responder4

Trials

Key trials

Large trials with a reported result on their main goal.

Running now

Other trials (11)

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

Trials where it is given as background therapy

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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