‘Reimbursed new drug for muscle disease SMA only under certain conditions’

by time news

The National Health Care Institute advises Health Minister Ernst Kuipers to reimburse the medicine risdiplam for the treatment of the hereditary muscle disease Spinal Muscular Atrophy (SMA) from the basic package. This is subject to the condition that only children and young people up to the age of 25 are eligible for reimbursement, because risdiplam has proven added value for them. Furthermore, the price has to be significantly reduced in negotiations with the manufacturer. This is reported by the National Health Care Institute.

The drug risdiplam (Evrysdi) has been shown to be effective in the treatment of children from 2 months to 25 years with the muscle disease SMA. These are people with type 1, 2 or 3 or people with 1 to 4 copies of the SMN2 gene who do not yet have symptoms of SMA. Treatment with the drug increases the chances of survival for young patients and significantly improves the movement and strength of the muscles. Patients must take risdiplam throughout their lives.

There is still insufficient evidence for the effectiveness of the drug for patients older than 25 years. The Zorginstituut will make an effort, together with the parties involved, to make risdiplam available to these patients through conditional admission.

Third drug for SMA

Risdiplam is the third drug to treat people with SMA. Onasemnogenic abeparvovec (Zolgensma) is a single gene therapy. This therapy can be used in babies who have been diagnosed with SMA through the heel prick screening and in children with SMA type 1. Nusinersen (Spinraza) is an SMA drug that is administered with an epidural. Because patients sometimes suffer from a deformity in the back, nusinersen cannot be applied to everyone. For them, treatment with risdiplam could be an option.

Price way too high

The costs of lifelong treatment with risdiplam are 4 to 7 million euros per SMA patient. The Zorginstituut concludes that the price is far too high to qualify for reimbursement from the basic package. This is partly due to uncertainties about the long-term treatment effects and because 2 other medicines are already available for SMA patients. That is why the Zorginstituut advises the minister to only include risdiplam in the basic package if the price falls sharply in negotiations with the manufacturer.

By: National Care Guide

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