How the hell do you demonstrate the graft and corruption of regulatory agencies, when THEY control the authorization of your drug, and when THEY are major investors in the mRNA vaccine manufacturers whose revenues will be smashed by lenz and the lenz-enhanced Novavax vaccine, and when THEIR scientists are receiving royalties, and when THEY are receiving the majority of their funding from their Big Pharma partners/sponsors?
Humanigen changed their primary endpoint to better align with the government's trial design.
Of course ACTIV-5 didn't meet the endpoint. The trial was designed to fail. We knew ACTIV-5 would fail, when CRP levels of the critically ill patients get >150mg/L of CRP.
Necessity, as I have always said, will lead to our authorization and approval. NOBODY believes in the mRNA vaccines, now that the truth about Serious Adverse Events are being reported. Pfizer trial patients had 36% more SAE's than the placebo group. And with a highly virulent strain of omicron (HIVICRON) expected, lenz will be the only safe and effective treatment on the market.
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