Not a chance we go all the way to 390 without an EUA. 22 states currently showing highest covid-19 test positive rate. That’s a lot of people that are soon going to fall into severe critical status and eventually death for many. It’s starting to surge in the U.S if our results show 20-30% mortality reduction that it’s already been extensively proven safe we will get EUA or Approval. In my opinion if with all the data we already have from EIND’s, CD-10 and CD-12 trails I am sure data is being unblinded Penalty or not and actively sending it to any country looking to reduce mortality numbers and length of hospital stay. How the FDA responds to the interim data will be very telling. If they don’t act quickly like within the next week I hope cytodyn puts metal to the pedal in all other interested countries manufacturing needs to be increased now not 2-3 months from now. With Remdesivir being the SOC and new studies coming out everyday about how Ineffective/safe it FDA needs a winner they are batting 0.000% (0 for 3)hydroxy Conv Plasma And Remdesivir. Tuesday biggest day in CYDY history!