Replies to post #77950 on Cytodyn Inc (CYDY)

[BioInvestor4]

Good morning! Until they submit double blinded trial results, or at least interim results. We cannot in expect the FDA to approve it. As good as the results are with the EIND patients, it’s anecdotal.

The good news is we very close to doing this. We only need 30 more patients in the mild/moderate trial. With 6 hospitals now on board, these 30 should be enrolled quickly. Without interims, I suspect we see these results in 30 days of less.

With Severe/Critical we need 25 more patients before interims. Because they need 28 days for patient results on this trial we may be 60 days away from results here.

In any event. There’s not much more we can expect from the FDA until we submit one of the two trial results.