I do think the FDA is the problem. I'm not 100% believing the FDA has denied our EUA due to BP influence, though IMO, it is "possible". I blame the FDA because if you add all our s/c data, m/m data, eIND data and HIV safety data, add all that to the severity of the global pandemic, and also the FDA terminology "may be effective", seems a reasonable person would agree the FDA is the problem!, the FDA will have a lot to answer for IMO. Their hesitation may truly be based upon Cytodyn being a zero revenue, very small, with no approvals, tiny new risky biotech. Also, the damage Cytodyn could incur upon BP, could effect BP revenue to such an extent as to harmfully reduce their research & development budgets, such that discovery of future medications to heal us, would be hindered.