I think because NP is not going to take this analy
Post# of 148173
Exhibit A from the PR
"Concurrently, we are seeking ongoing guidance from the U.S. Food and Drug Administration and regulatory agencies in other countries for a swift regulatory approval pathway for leronlimab to treat COVID-19"
I'm thinking they are letting everyone know that another interim analysis was recommended at a lower patient count....Hey FDA wake up we're almost there, should we let more people die to hit your "special number" or can we stop this right now? I mean remdesivir was "trending", so are we.