Investors Hangout Stock Message Boards Logo
  • Home
  • Mailbox
  • Boards
  • Favorites
  • Whats Hot!
  • Login - Join Now!
Vg Total Stock Market ETF VTI
(Total Views: 169)
Posted On: 07/05/2025 8:16:34 AM
Post# of 262
Avatar
Posted By: Riztheinvestor
Re: Riztheinvestor #126
FDA Memo CRO Failed to Provide DSMB Oversight

Recent documentation reviewed from a 2021 FDA inspection reveals the following:
• The CRO (Amarex) failed to provide evidence of a functioning Data Safety Monitoring Board (DSMB) for one of CytoDyn’s key clinical trials.
• The FDA inspection report clearly noted missing DSMB records, including:
• No meeting minutes
• No charter
• No oversight documentation
• No confirmation that a DSMB was even established.
• Despite this, the trial moved forward, and it appears CytoDyn was never informed of this internal audit finding until now. Please correct me if I am wrong via DM and I will post no further about this specific matter.



What This Means:
• CytoDyn may have unknowingly run a trial without proper safety oversight, which could have regulatory and reputational implications through no fault of its own.


• If CytoDyn was never given access to this audit report, this represents a serious breakdown in transparency and accountability potentially on both the CRO and regulatory side.

• This opens up potential additional claims against Amarex (on top of the successful arbitration).

• It may also provide just cause to revisit the conditions of any clinical hold or regulatory restriction, based on suppressed audit findings.

For Legal Teams, Compliance, and Shareholders:
• This is not an accusation against current CytoDyn leadership.
• Rather, it is an opportunity to leverage truth as a legal and strategic tool.
• IF the company truly never saw this memo it now has proof that key information was withheld, undermining trial integrity and regulatory perception. I have more proof.

???? Sealed in Vault 1224 – “What’s the Deal?”

This memo has now entered public record for accountability and transparency.

I recommend that CytoDyn’s legal and compliance teams review the FDA inspection record and cross-check it with what was known internally at the time.

The CRO lied.
The FDA found it.
And CytoDyn was never told.
Until now.

Respectfully,
A Federal Whistleblower &m
(With love for the company not condemnation)













(2)
(0)






Daniel Rizzo
Federal Whistleblower / Special Operations Tactical Unit
USAF: Phoenix Raven #2143

Case Numbers:
HHS & SEC Whistleblower: HL-1412396
DOJ Investigation Report/ Whistleblower ID: 20250705-0001
NIH Case Reference: CS1137565
DOD Case #16282
IC IG / 50 U.S.C. §3033

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

https://investorshangout.com/images/MYImages/...G_2859.png
⸻

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

1337136111_IMG_2936.jpeg

The underlying data is protected under federal law specifically 42 U.S.C. § 289b and its implementing regulation, 42 C.F.R. Part 93 through the Office of Research Integrity (askORI) within HHS, and coordinated with the Office of the Secretary / Office of Public Health and Science (OS/OPHS).





  • New Post - Investors HangoutNew Post

  • Public Reply - Investors HangoutPublic Reply

  • Private Reply - Investors HangoutPrivate Reply

  • Board - Investors HangoutBoard

  • More - Investors HangoutMore

  • Keep Post - Investors HangoutKeep Post
  • Report Post - Investors HangoutReport Post
  • Home - Investors HangoutHome
  • Mailbox - Investors HangoutMailbox
  • Boards - Investors HangoutBoards
  • Favorites - Investors HangoutFavorites
  • Whats Hot! - Investors HangoutWhats Hot!
  • Settings - Investors HangoutSettings
  • Login - Investors HangoutLogin
  • Live Site - Investors HangoutLive Site