Not meaning to wade into someone else's debate. But does the content of the interim results for Travere's Phase 3 FSGS trial for Sparsentan shed a bit more light on this discussion. I'm expecting something similar from DXB in mid-March. This was almost an identical interim milestone which had a specific proteinuria endpoint and references statistical significance.
Link to their interim results announcement - here
Ann: Application for quotation of securities - DXB, page-112
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