You are correct CDiddy that the trial size will be
Post# of 148173
Now...if they wanted to pursue a trial to retest for primary endpoint (from P2 trial), they would need to increase the population size to get beyond clinically significant to statistically significant. But why? They already have statistically significant result with secondary endpoint (NEWS2).
I found this circular logic illogical. My thinking is that even CYDY's doctors have no idea why the EFF-DA would reject the EUA other than the EFF-DA doing what it's been doing to them...EFFing with them.