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CytoDyn Inc CYDY
(Total Views: 640)
Posted On: 03/05/2021 10:22:27 PM
Post# of 155594
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Posted By: Riztheinvestor
Worth a repost.



Some folks are not paying attention to the FDA. Here is a summary of FDA Director Janet Woodcock’s comments about S/C Treatments and drugs:

- The FDA acknowledged that normal P-Factor is not the bar they want to set to evaluate Treatments for S/C during a pandemic.

- If any Treatment shows good improvement over SOC for S/C patients, the FDA will be inclined to offer an EUA and continue evaluating said Treatment for either full approval or discontinuance of the EUA.

- S/C patients have no choice. Any Treatment that is SAFE and gives them a better chance of survival WILL receive an EUA as the alternative is death.

- The FDA will be looking to pair up viable drugs to improve that chance of survival through partnerships.













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Daniel Rizzo
Federal Whistleblower / Special Operations Tactical Unit
USAF: Phoenix Raven #2143
HHS & SEC Whistleblower: HL-1412396
DOJ Investigation Report/ Whistleblower ID: 20250705-0001
NIH Case Reference: CS1137565


Founder & CEO of FireGate Bioscience
USPTO: Lead Inventor of the HIV Cure & AI Federal Oversight Program

⸻

Public Links
FireGate Bioscience: https://www.firegatebioscience.com
NotYourDrug.com: https://www.notyourdrug.com



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