*Exibit E: April 27th, 2020 Page says 20 of 44 Dr.

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My69z
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*Exibit E:

April 27th, 2020
Page says 20 of 44

Dr. J e-mailed Fredrick Hayden & made it clear about LL.

Hayden was the Gilead consultant on the Safety Brd.

Dr. J CC'd clinton & gates foundations & included Cytodyn people

*Exhibit G:
FDA saying"Complete BLA" news release total lie & mentions why. Said if they think it's complete, could a RTF notice that day.

*Exhibit J:
Shows the collab with other depts on the BLA decisions, & instructions to KK, although saying it's laced with "definicies)" .....but they thank others for helping

Horrible exhibit for Amarex

*Exhibit G, page 2 of 2:
Pulling back on EINDs so can enroll into trials

*Exhibit H April 19th, 2020 e-mail:

Dr. J pushed back to Murray about judging Cytodyn harshly

That was followed by the gag with spoon replies, to Murray.

*June 5th, 2024 trial starts

* Exhibit J e-mail.
April 27th, 2020.
Dr. J's outstanding covid e-mail to
Gates, Clinton & others.

On e-mail, Murray offered to also send to WHO.

Followed by internal e-mail frwd'd to co-workers:

" Gag me with a spoon. Why is Linda Lewis on the cc list. This is all worthless data. Unless i see controled data, i will never ever believe it"

So far, that is the only known line of thinking from him & it's not criminal, per say.

* Exhibit K
April 29th, 2020.

When NP pr'd a complete BLA was filed. She not only internaly talked about how it was a lie, but this is a very key comment ----

" Total lies, they did not submit any clinical datasets & they are not expected until May".

So telling shareholders it's "complete", & AHEAD of the extra timeframe they were given.

They for no reason, lied, in advance.

Her comment continues:

"Technically, they should have only submitted module 5 when it was complete with datasets. They still havent given us the DSMB charter. DSMB meeting minutes, (open session & closed session), analysis results/reports presented to DSMB --- we've asked for this multiple times. I'll need to call them today to explain tge clock has not started and they dont have a complete submission. If they think the submission is complete we can send a refusal to file letter today".

Based on that NP press release, RTF letter if FDA was truly treating them with intent/malice, was warranted. But in all their e-mail "insults" so far, they never talk about intentionally delaying, etc.. Always mention what is missing, incorrect, instructing, have offered step by step clarity & many things on repeat. No wonder structured settlement talks to start.

These e-mails are only getting worse for Amarex & not supporting his --- "yea, i watched the dog eat my homework, but you should've helped me".

BLA was a disaster & FDA thought LL would do harm in covid. Even Dr. J & Patterson said during covid--- FDA simply dosen't understand LL.

These e-mails only show Amarex owing Cytodyn more & more in damages. Hell, FDA even questioned his duties to Cytodyn!

Eventually all this bullshit will come to pass

Shall see.....





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