Two days to discuss: nothing. There is no human data on how these newly formulated vaccines work

CDC has scheduled its ACIP Advisory Committee meeting for Sept. 1 and 2 to sign off on the new Omicron boosters.

The normal notice was not provided in advance of this meeting.

In accordance with 41 CFR 102-3.150(b), less than 15 calendar days’ notice
is being given for this meeting due to the exceptional circumstances of
the COVID-19 pandemic and rapidly evolving COVID-19 vaccine development
and regulatory processes…

Matters To Be Considered: The
agenda will include discussions on use of COVID-19 vaccines booster
doses. A recommendation vote(s) is scheduled. Agenda items are subject
to change as priorities dictate.

Procedure for Oral Public Comment: All persons interested in making an oral public comment during the September 1-2, 2022, ACIP meeting must submit a request at https://www.cdc.gov/​vaccines/​acip/​meetings/​ no later than 11:59 p.m. EDT, August 30, 2022, according to the instructions provided.

What’s the hurry? There is barely any COVID. New cases are at their lowest level in 3 months. ICU cases have been way down for a full 6 months.

While
it is legal for FDA to omit convening its advisory committee when it
makes an important decision, such as authorizing new boosters—without
requiring so much as a phase 1 trial in humans—the ACIP (CDC’s advisory
committee on immunization practices) and not the CDC itself makes the
vaccine recommendations for the entire United States. Then the CDC
Director signs off on them. So CDC could not get around convening this
ACIP meeting. FDA isn’t convening one because probably Paul Offit and
other members would give FDA a blast of truth about such a bold and
reckless move: approving vaccines for widespread use before even the
shoddiest Phase 3 trial in humans had been performed.

Last
year the Director overruled her advisory committee on the adult
boosters. Which is unheard of. Rochelle must have been getting her
marching orders from God, no Fauci, no Schwab or whoever gives the Great Reset orders, I guess.

So,
this is a tricky situation for the ACIP and the Rochelle windup doll.
The USG has already ordered about 180 million doses from Pfizer, and
some unknown amount from Moderna. So the rollout plan has to be
approved by the ACIP Committee.

Last time this happened, the
federal government announced its purchase of boosters the day after the
FDA advisory committee met. When committee member Paul Offit was later
interviewed by Z-Dogg, Offit described the meeting, then the booster
vaccine purchase announced the next day, and Offit told Z-Dogg, “The Fix Was In.”

He
also told Z-Dogg how it took 20 years to develop the rotavirus vaccine, and
then how “nauseating” it was when it rolled out, wondering what side
effects it might cause (minute 46). 

This time, the bold and the
reckless Biden flunkies didn’t even wait for the meeting to be held, and
pre-bought the vaccine ahead of time. If that is not signalling to the
members how they are expected to vote, I don’t know what is.

Normally
the Committee members show extreme docility regarding the votes CDC
wants them to take, even if it means lots of babies will die who didn’t
need COVID shots in the first place. However, this is the first time in
history a totally new vaccine is to be pushed through the ACIP with no
human trials. 3 months ago, it had not even been designed.

Flu shots are slightly adjusted each year, and essentially grandfathered in. But
they get used in the southern hemisphere first, so the north (us) gets
the benefit of essentially six months of trials down under.

But in this case, for the first time in history, the new boosters with mRNA for omicron BA.4/5 plus the old mRNA vaccine formulation have been through no trials at all.
Pfizer only applied for the right to perform clinical trials on Monday
Aug. 22 and on August 25 said they had not started yet.

So,
it is the ACIP that is to be left holding the bag on this one. Will
they suck it up and vote yes? Will they bleat a little, then vote yes?
Or will they realize they have been positioned to take the fall and
actually ponder the meaning of their vote?

I will live
blog the ACIP meeting for Children’s Health Defense. Please join me,
and let’s do our best to witness what they try to pull off.

I have also applied to speak during the public comment section. Will I be blocked again?

Here
is another wrinkle. Four of the 15 ACIP members are supposed to have
completed their 4 year terms on June 30, though their names are still
listed on the ACIP roster and they were part of a meeting last month. I
think they will be gone at the next meeting, and a new group replacing
them will have already been vetted to make sure there are no glitches
with this upcoming vote. We won’t know who they are, probably, until
September 1. Here are the likely departing members:

AULT, Kevin A., MD, FACOG, FIDSA
Professor and Division Director
Department of Obstetrics and Gynecology
University of Kansas Medical Center
Kansas City, KS
Term: 10/26/2018 – 6/30/2022

KOTTON, Camille Nelson, MD, FIDSA, FAST
Clinical Director, Transplant and Immunocompromised Host Infectious Diseases
Infectious Diseases Division, Massachusetts General Hospital
Associate Professor of Medicine, Harvard Medical School
Boston, MA
Term: 12/23/2020 – 6/30/2022

MCNALLY, Veronica V., JD
President and CEO
Franny Strong Foundation
West Bloomfield, Michigan
Term: 10/31/2018 – 6/30/2022

TALBOT, Helen Keipp, MD
Associate Professor of Medicine
Vanderbilt University
Nashville, TN
Term: 10/29/2018 – 6/30/2022