HSE decides against approving drug for rare muscle-wasting disease

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HSE decides against approving drug for rare muscle-wasting disease
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Spinraza is only treatment available for those with spinal muscular atrophy

drugs group has again decided against approving the only treatment on the market for the rare muscle-wasting disease spinal muscular atrophy .

The application by Biogen will now be considered by the HSE leadership team in early June, he told the Oireachtas health committee. Ms Conway-Walsh said it was “wholly unacceptable” that Spinraza was approved in the UK but not in Ireland. “Time is of the essence” as some of the children who urgently need the drug are “shutting down”.

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