The “Future Framework” is coming from the World Health Organization, and the Bill & Melinda Gates Foundation is the biggest voluntary contributor to the WHO, so Gates is likely directing the play.
Introduction: The FDA always rigs the game on behalf of Pharma
Late Friday afternoon, the FDA released its agenda for the Vaccines and Related Biological Products Advisory Committee (VRBPAC) meeting that will vote on the Orwellian “Future Framework” on Tuesday, June 28.
Then on Saturday morning, the FDA released a briefing document in connection with this scheme to end science as we know it in connection with future COVID-19 shots. (Much appreciation to the brilliant James Roguski for alerting me to these documents.)
In this article, I will explain what is in the briefing document, what is likely to happen at the meeting and what can be done about it.
The FDA’s ‘Future Framework’ briefing document
The briefing document is 18 pages of text, 1.5 line spacing, with just 19 references — 9 of which are pre-prints or from the CDC’s in-house newsletter Morbidity and Mortality Weekly Report (MMWR) which means they are not peer-reviewed.
Any true believer in The Narrative(TM) could have written this in a few hours. To base the entire future of COVID-19 shots on this glorified undergrad term paper is madness.
As I predicted, even though the April 6 meeting was presented as an exploratory initial conversation that reached no conclusions whatsoever, the “Future Framework” is now being presented by the FDA as a done deal, fait accompli, you’d have to be crazy to insist on proper safety studies.
The core argument of the briefing document is hilarious (or rather, it would be hilarious if it was not a plan to permanently institutional genocide and hide the evidence). In several places the FDA argues (colloquialisms mine):
1. These COVID-19 shots work great, miracles really, incredibly effective, boy howdy do they work well! Boosters too, total home run, the Israelis even have 10-weeks of data showing that they might help old people. What more evidence could you want?
2. Okay, well, it depends on what you mean by work. These shots do not stop infection, transmission, hospitalization, or death, even though that’s why we licensed them. Any protection wears off fairly quickly, but It’s Not Our Fault(TM) because This Wily Virus(TM) mutates too fast and no one told us that it would ever mutate.
The briefing document literally states:
“The evaluation of modified vaccines for the purpose of vaccine strain composition decisions will need to rely mainly on comparative immunogenicity data due to the time constraints involved in vaccine manufacturing and clinical efficacy evaluation.”
Did you catch that? The evaluation “will need to rely on” (no decision to be made here) measures other than actual health outcomes because of “time constraints.”
Moderna, Pfizer and Novavax are all developing reformulated COVID-19 shots. But they know that the FDA is not going to look at health outcomes so they are going to great lengths to jack up the antibody response.
Pfizer tested a double-strength dose (60 mcg of mRNA instead of 30 mcg) even though they had previously ruled out a higher dose because of safety concerns. So the antibody levels are through the roof.
But the VRBPAC admitted on April 6 that there are no known correlates of protection (meaning: antibody levels do not tell you who will be immune) so these antibody measures are medically meaningless.
Sane people realize that if you turbo charge the immune response, you may also turbo charge adverse events. But the “Future Framework” allows pharmaceutical companies to skip clinical trials altogether.
Furthermore, all of these companies are developing shots to target the original Omicron strain (BA.1) even though it has already been supplanted by other variants (BA.4 and BA.5).
The FDA and these companies claim that shots targeting BA.1 will be effective against later variants but I do not know how they can possibly argue that given the total absence of actual health data.
Words that you will NOT find in the FDA “Future Framework” briefing document:
- original antigenic sin,
- antibody-dependent enhancement,
- prion disease,
- adverse events, or
- side effects.
So the FDA is literally not looking out for any of the worst-case scenario possibilities.
The “Future Framework” is a plan to base the entire COVID-19 vaccine program on magical thinking rather than science.
What’s likely to happen at the VRBPAC meeting on Tuesday, June 28
The cartel is predictable because they follow a playbook and they use the same cast of characters over and over again.
None of their data will be peer-reviewed so it will all be fanciful fiction — 95% to 100% efficacy based entirely on belief.
If the FDA stated plainly what they are up to there would be riots.
What is to be done
We only have about 24 hours to act so let’s leave it all on the field!
Please submit a formal comment to the regulations.gov website stating that the FDA must reject the “Future Framework” and that all reformulated COVID-19 shots must go through proper human clinical trials. The docket number is FDA-2022-N-0905.
The docket will close Monday night June 27 at 11:59 Eastern time. Click here to go to the relevant page on the regulations.gov website and look for the blue comment button in the upper left-hand corner.