How it works: Calming and slowing immune cells →

Vumerity

EU: Approved in the EU since 2021US: FDA approved 2019

Molecule type
Small molecule
Mechanism (ChEMBL)
Kelch-like ECH-associated protein 1 inhibitor
Targets
Kelch-like ECH-associated protein 1
Availability
Authorised in all EU and EEA countries. Reimbursement is decided by each country.

Approvals

  • USVumerity · Approved2019-10-29 Source
  • EU/EEAVumerity · Authorised2021-11-15 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.

11,848 reports in total, 4,590 marked serious.

  • Flushing1,611
  • Multiple sclerosis1,099
  • Multiple sclerosis relapse973
  • Diarrhoea873
  • Product dose omission issue820
  • Fatigue781
  • Nausea753
  • Headache619
  • Pruritus590
  • Memory impairment566

Trials

Key trials

Large trials with a reported result on their main goal.

Running now

  • VOYAGE

    Not yet recruiting · Phase 3 · Relapsing MS · ongoing

  • DESIRE MS

    Recruiting · Phase 3 · Relapsing and progressive · ongoing

  • TWINS

    Not yet recruiting · Phase 3 · Relapsing MS · ongoing

  • Dimethyl fumarate

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

  • Dimethyl fumarate

    Recruiting · Relapsing MS · ongoing

  • Dimethyl fumarate

    Running, not recruiting · Relapsing MS · ongoing

  • Alemtuzumab

    Running, not recruiting · Relapsing MS · ongoing

Other trials (7)

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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