(Total Views: 604)
Posted On: 05/30/2021 2:08:09 PM
Post# of 154090
Theories relating to why Brazil, India and the Philippines are not obtaining massive quantities of leronlimab for "Compassionate Use". What why not?
This remains a huge mysterious mystery? Why not reports of the 128 critical patients in the Philippines who received free Leronlimab for Compassionate Use? This is massivenly suspicious of FDA/BP influence in these 2 countries IMO.
FDA letter attacking Leronlimab? Why? Come On Man? Why? What is behind the decision to put out that strange, unprecedented powerful letter?
Extreme conspiracty theory that the virus was intentionally released to diminish global population.
Theory that if a therapeutic would be approved, even more folks would refuse a vaccine, and we must first get the planet vaccinated.
Theory that FDA and BP didn't want a therapeutic for severe or critical approved, because vaccine manufacturers and Gilead's remdesivir would loose money.
Theory that FDA and BP didn't want leronlimab approved because it would take profits from Gilead for remdesivir and HIV and cancer, and just possibly generally devastate too many major BP players, with all the indications for this miracle molecule leronlimab, produced by this tiny, unknown, zero revenue biotech firm with no connections to money movers.
Theory that FDA intentionally "controlled" CD12 protocol to a limit of only 2 doses, fully knowing and or expecting that 3 and 4 doses would lead to a p value < 0.05
This remains a huge mysterious mystery? Why not reports of the 128 critical patients in the Philippines who received free Leronlimab for Compassionate Use? This is massivenly suspicious of FDA/BP influence in these 2 countries IMO.
FDA letter attacking Leronlimab? Why? Come On Man? Why? What is behind the decision to put out that strange, unprecedented powerful letter?
Extreme conspiracty theory that the virus was intentionally released to diminish global population.
Theory that if a therapeutic would be approved, even more folks would refuse a vaccine, and we must first get the planet vaccinated.
Theory that FDA and BP didn't want a therapeutic for severe or critical approved, because vaccine manufacturers and Gilead's remdesivir would loose money.
Theory that FDA and BP didn't want leronlimab approved because it would take profits from Gilead for remdesivir and HIV and cancer, and just possibly generally devastate too many major BP players, with all the indications for this miracle molecule leronlimab, produced by this tiny, unknown, zero revenue biotech firm with no connections to money movers.
Theory that FDA intentionally "controlled" CD12 protocol to a limit of only 2 doses, fully knowing and or expecting that 3 and 4 doses would lead to a p value < 0.05
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