The lottery system — which has been called a managed access program — would establish a bi-weekly draw for babies under the age of two who live in countries where Zolgensma is not approved.
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Those who are not chosen will simply stay in the program until they are no longer medically eligible.The British advocacy group TreatSMA has expressed concern with the program, which it describes as akin to picking “lucky” kids to receive the life-saving drug over others.
“We are yet to be convinced that a health lottery is an appropriate way of meeting the unmet medical needs in this severe disease,” the group said in a statement.
AveXis , the subsidiary that developed the drug, says that the program was created in response to growing demand for the drug outside of the US, where it was approved by the Food and Drug Administration in May.
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The company is still trying to register the drug in around three dozen companies.The dosage lottery is set to start on 2 January, and AveXis has said the program was created with the advice of a “bioethics advisory committee”, and manages manufacturing constraints. Just two drugs for spinal muscular atrophy are approved in the US. The other, called Spinraza , requires recurring doses. The first costs $750,000 for the first year, and $375,000 each following year.