There is no valid excuse for FDA to not approve this therapy right now. Who are they protecting? What has anyone got to lose? So far we know the side effects are clearly very low or near zero. All the anecdotal evidence (and the s/c Interim results surely) shows it saves C/S patient lives. It may save an additional 5% or it may save an additional 70% of those who are going to die. We know it will not create additional medical problems. The FDA is allowing deaths to continue IMHO. If we have EUA then FDA can take all the time they want. Possibly s/c covid patients in the USA may shun the clynical trials but there will be real result broadcasted on EUA results world wide, Fox News+ etc. Let the UK build our s/c trial enrollment, with less help from us, because we are saving lives and spreading the word, from our EUA compelling, world changing results. That's my urgent preference. But I believe we will be hearing at any minute that another nation has granted some type of approval and will be buying vials of Leronlimab, and that will be second choice, but it will bring about a series of positive events. Nader said yesterday (posted on NASDAQ.com that he is actively talking with regulatory agencies in other nations about pathways for approvals!!!!!!!!!! YAY! Go for it Nader, you have the data and results to get that done.