correct
One has to ask the question ?
If Per don’t meet the Primary PUL2.0 endpoints
but show the secondary muscle function improvement .. is that enough to get FDA approval?
We know the boys on trial now are pressing on past the 6 month dosing is an indication that it’s showing benefits .
all good
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- FDA approves Sareptas Srp901 for the whole population
FDA approves Sareptas Srp901 for the whole population, page-9
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