Decision to fund treatment earlier for relapsing remitting multiple sclerosis
What we’re doing
We're pleased to announce that access to eight treatments currently funded for relapsing remitting multiple sclerosis will be widened from 1 July 2022. This means that some people will be able to access funded treatment earlier, after only one clinical attack of multiple sclerosis.
We anticipate that around 110 people will benefit from earlier treatment with multiple sclerosis treatments in the next five years as a result of this decision. The eight currently funded treatments for multiple sclerosis we are widening access to are:
- dimethyl fumarate (Tecfidera)
- fingolimod (Gilenya)
- glatiramer acetate (Copaxone)
- interferon beta-1-alpha (Avonex)
- interferon beta-1-beta (Betaferon)
- natalizumab (Tysabri)
- ocrelizumab (Ocrevus)
- teriflunomide (Aubagio)
Any changes to the original proposal?
This decision was subject to a consultation letter dated 19 May 2022. You can read the consultation here.
There have been no changes to the proposal following consultation.
Who we think will be most interested
- People with multiple sclerosis and their whānau
- Healthcare professionals involved in the management of multiple sclerosis
- Advocacy and patient support groups
- Community and hospital pharmacies and DHBs
- Suppliers and wholesalers
Detail about this decision
Clinicians use the Revised McDonald Criteria(external link) to help diagnose multiple sclerosis. The McDonald criteria were most recently revised in 2017, following an update from the McDonald criteria of 2010. One of the main differences between the 2017 and 2010 criteria is that with the 2017 criteria people may be formally diagnosed with multiple sclerosis after one clinical attack of multiple sclerosis (also known as clinically isolated syndrome, CIS).
This decision has updated the access criteria to include the 2017 McDonald criteria, so that people can access treatment sooner than they can now (currently a person has to experience another attack (ie. a relapse) before they can receive funded treatment).
The access criteria will be updated in Section B and Part II of Section H of the Pharmaceutical Schedule from 1 July 2022 to the following (changes to current criteria in bold and strikethrough):
Special Authority for Subsidy
Initial application — (Multiple sclerosis) Applications only from a neurologist or general physician. Approvals valid for 12 months for applications meeting the following criteria:
All of the following:
- Diagnosis of multiple sclerosis (MS) meets the McDonald 2017 diagnostic criteria for MS and has been be confirmed by a neurologist. Diagnosis must include MRI confirmation; and
- Patients must have Clinically Definite Relapsing multiple sclerosis with or without underlying progression; and Patient must have has an EDSS score 0 - 6.0; and
- Patient has had at least one significant attack relapse of MS in the previous 12 months or two significant attacks relapses in the past 24 months; and
- All of the following:
- Each significant attack relapse must be confirmed by the applying neurologist or general physician (the patient may not necessarily have been seen by them during the attack relapse, but the neurologist/physician must be satisfied that the clinical features were characteristic); and
- Each significant attack relapse is associated with characteristic symptom(s)/sign(s) or substantially worsening of previously experienced symptoms(s)/sign(s); and
- Each significant attack relapse has lasted at least one week and has started at least one month after the onset of a previous attack (where relevant); and
- Each significant attack relapse can be distinguished from the effects of general fatigue; and is not associated with a fever (T> 37.5°C); and
- Either:
- Each significant attack relapse is severe enough to change either the EDSS or at least one of the Kurtze Functional System scores by at least 1 point; or
- Each significant attack relapse is a recurrent paroxysmal symptom of multiple sclerosis (tonic seizures/spasms, trigeminal neuralgia, Lhermitte’s symptom); and
- Evidence of new inflammatory activity on an MRI scan within the past 24 months; and
- Any of the following:
- A sign of that new inflammatory activity on MRI scanning (in criterion 5 immediately above) is a gadolinium enhancing lesion; or
- A sign of that new inflammatory activity is a lesion showing diffusion restriction; or
- A sign of that new inflammatory is a T2 lesion with associated local swelling; or
- A sign of that new inflammatory activity is a prominent T2 lesion that clearly is responsible for the clinical features of a recent attack relapse that occurred within the last 2 years; or
- A sign of that new inflammatory activity is new T2 lesions compared with a previous MRI
Note: Natalizumab can only be dispensed from a pharmacy registered in the Tysabri Australasian Prescribing Programme operated by the supplier. Treatment on two or more funded multiple sclerosis treatments simultaneously is not permitted.
Renewal — (Multiple sclerosis) only from a neurologist or general physician. Approvals valid for 12 months where patient has had an EDSS score of 0 to 6.0 (inclusive) with or without the use of unilateral or bilateral aids at any time in the last six months (i.e. the patient has walked 100 metres or more with or without aids in the last six months).
Note: Natalizumab can only be dispensed from a pharmacy registered in the Tysabri Australasian Prescribing Programme operated by the supplier. Treatment on two or more funded multiple sclerosis treatments simultaneously is not permitted.
Our response to what you told us
We’re really grateful for the time people took to respond to this consultation. A summary of the main themes raised in feedback and our responses to the feedback received are available below:
Theme |
Pharmac comment |
---|---|
Overwhelming support for the proposal, with no proposed amendments to the access criteria. Many responders commented that this proposal would bring New Zealand in step with international guidelines and shared personal stories explaining their experience or that of their whānau with multiple sclerosis and what earlier treatment would mean for people who are newly diagnosed. |
We are grateful to all the people who wrote in to tell us about their experiences with multiple sclerosis and what earlier treatment would mean to them and their whānau. Hearing how medicines impact the lives of New Zealanders is really important in helping us understand the value of the medicines we are proposing to fund. |
Request for funding for medicines to treat primary progressive multiple sclerosis (PPMS), including fampridine. |
We acknowledge that there are currently no funded treatments for PPMS and that there is a large unmet health need. A proposal to fund ocrelizumab for PPMS has been considered and is ranked on our options for investment list(external link). You can see the progress of this proposal on the Application Tracker here(external link). At this time and taking into account the amount of investment funding available, we are focussing on progressing funding options that are currently ranked higher than ocrelizumab for PPMS. Our ability to fund ocrelizumab for PPMS would depend on it being the next best investment and within the available budget. We have also assessed a proposal to fund fampridine for symptomatic walking improvement for MS. PTAC recommended that the application be declined [PDF, 290 KB]. We would welcome any updated information for this to be reconsidered. |
This proposal will result in an increased need for infusion services, where there are currently significant issues with capacity. |
Pharmac staff acknowledge that this proposal could increase use of infusion services required for a small number of patients. We note that many people who will benefit from this decision may be initiated on treatment options which do not require infusion. |
Pharmac should consider the impact of climate change and waste minimisation in its factors for consideration. |
Pharmac recognises that the global manufacture, transportation, disposal and packaging of medicines and medical devices impacts the environment. While very little pharmaceutical manufacturing occurs in New Zealand, there are still good opportunities to improve sustainability through procurement. Pharmac’s work is part of the Government’s commitment to climate change action(external link). We currently consider broader outcomes (including environmental sustainability) in our procurement processes and seek this information from suppliers as part of our evaluation. We continue to develop this work and are planning to engage with stakeholders in the near future in this area. |
If you have any questions about this decision, you can email us at enquiry@pharmac.govt.nz; or call our toll free number (9 am to 5 pm, Monday to Friday) on 0800 660 050.