01/06/2026
A New Motor Neuron Disease (MND) drug is showing reductions in key disease markers, slowing the progression of the disease in patients with a particular genetic mutation and providing hope to families.
Through monthly injections, the new drug binds to messenger RNA, reducing the number of harmful SOD1 (Superoxide Dismutase 1) proteins that build up in the nerve cells and which cause MND in up to 2% of all cases.
The growing urgency of treating the disease as well as the promising data from the drug, has prompted the Therapeutic Goods Administration to grant provisional approval of the drug, enabling Australian patients’ faster access.
Speaking with Channel 9, NeuRA CEO Professor Matthew Kiernan AM emphasised the importance of early intervention leading to more positive outcomes when it comes to MND.
"The availability of a targeted treatment reinforces the need for clinicians to act with urgency; any suspicion of MND should prompt immediate referral to a neurologist or specialist centre," said Professor Kiernan.
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