Muscular Dystrophy wants Spinraza to be made available on the NHS – The National

DRUG bosses must approve a “lifeline” drug for use on the NHS to stop patients losing the power to move, breathe and swallow, a charity has said.

Muscular Dystrophy UK is urging the Scottish Medicines Consortium (SMC) to make Spinraza available to patients with a rare muscle-wasting condition called spinal muscular atrophy (SMA).

The most acute form carries a life expectancy of around two years. More than 100 people in Scotland have some form of SMA and the charity says the drug, which is the only one of its kind, could “buy families time to spend with their loved ones”.

It is currently provided to some young patients in Scotland through a temporary scheme. The SMC will next rule on whether to approve the treatment for use on the NHS.

Ahead of a meeting with officials today, Muscular Dystrophy UK chief executive Robert Meadowcroft said: “Some children who have received Spinraza have seen their muscle strength improve and have already lived long enough to crawl, and even walk. For parents, this is priceless.

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