Ann: FDA confirms Proteinuria as Primary Endpoint for US approval, page-13

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    The statement open to discussion on endpoints that could support a potential Accelerated Approval application and verify clinical benefitpresenting earlier market entry bodes well. I read that to be an industry standard benchmark that was not previously established. Might dosage adjustments be the catalyst to this? I'm not sure, but further updates will no doubt follow.
 
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