Disease index

neuromyelitis optica spectrum disorder

Neurology · 2020–2024

3decisions
2medicines
3carried consumer input
3individual submissions

Every decision

MedicineMeetingOutcomeConsumer input
ravulizumab Treatment of adult patients with neuromyelitis optica spectrum disorder (NMOSD) who are aquaporin-4 (AQP4) antibody positive, who have experienced a recent… Nov 2024 Recommended with restriction 3 individuals
eculizumab Treatment of patients with neuromyelitis optica spectrum disorder (NMOSD) who are aquaporin-4 positive (AQP4+) with an Expanded Disability Status Scale (EDSS)… Nov 2021 Not recommended input received MS Australia
eculizumab Treatment of patients with neuromyelitis optica spectrum disorder (NMOSD) who are aquaporin-4 (AQP4) positive and who have either frequent relapses or a prior… Nov 2020 Not recommended input received MS Australia · MS Research Australia

Who spoke

MS Australia · MS Research Australia

What the PBS pays

$143M in government benefit over 2024–25, across 2,593 services.

This is spend on the medicines considered for this condition, not spend on the disease. A medicine used for several conditions is counted in full under each, so figures across conditions add to more than national PBS expenditure.

MedicineGovernment benefit
ravulizumab $105.7M
eculizumab $37.1M

Appraised elsewhere

NICE, in England and Wales, has appraised 2 technologies for this condition, recommending 0 . A different committee, a different population and a different price: this is what has been looked at there, not a verdict on what happened here.

TechnologyAppraisalOutcomeDate
satralizumabSatralizumab for preventing relapses in neuromyelitis optica spectrum disorders (terminated appraisal) TA960 terminated 2024-03
eculizumabEculizumab for treating relapsing neuromyelitis optica (terminated appraisal) TA647 terminated 2020-09

Registered, not subsidised

Medicines on the ARTG for this condition with no PBAC record at all. Registration and subsidy are separate decisions: a medicine can be legally available in Australia and never have been put to the committee.

MedicineOn the ARTG sinceRegistrations
inebilizumabUPLIZNA inebilizumab 100 mg/10 mL concentrated injection vial 2025 1
satralizumabENSPRYNG satralizumab 120 mg/1 mL solution for injection in pre-filled 2020 1

The ARTG export holds current registrations only, so the year is the earliest entry still on the register rather than a first-registration date. The condition here comes from the registered label, which is usually broader than the population a sponsor asks to have subsidised.

Conditions are classified by a language model from the indication text of each submission, so an individual label here can be wrong. Consumer input is read from the document's own consumer comments section: 3 of 3 decisions since 2014 carried some. Silence means no comment reached the committee through that facility, not that nobody was affected. More on how this was built.