IT WAS A PERFECT CARTEL ARRANGEMENT
The Defender Show’ Episode 62: Moderna Clinical Trials Terribly Flawed — and FDA Knew It, Sasha Latypova Tells RFK, Jr.
In this video RFK Jr. Interviews Sasha Latpova, a 25 yr., research and development executive in the pharmaceutical industry who understands creating and reviewing data to submit to the FDA, as this was part of her job.
She uncovers evidence through a FOIA request, of criminal findings against the FDA, the NIH, Moderna, and others. Which pre meditated murder and genocide, are charges that can NO LONGER be overlooked.
As Sasha put it, "It was a perfect cartel arrangement."
Sasha charges the FDA & NIH, of knowing of the terrible terrible flaws in the Moderna trials, yet still - licensed to sell the Moderna MRNA vaccine.
[LICENSED TO KILL]
The trials do not prove safety, far from it. It's a very dangerous vaccine product, and they used very deceptive means to conceal the warning signals in the studies.
Sasha meticulously analyzes 699 pages of the test results.
Her first point - Moderna's non clinical summaries contain irrelevant, unrelated material. [OVER 400 PAGES], and as she put it, they seemed to be trying to achieve a minimum word count.
These 400 pages contained a vaccine that was completely unrelated to SARS COV 2. An unrelated vaccine took up over 400 pages! And yet they subbmitted it as though it was the vaccine needing approval.
This particular entity contained 6 different MNRA constructs, had nothing to do with covid, and it WAS NEVER APPROVED, meaning It FAILED. THIS WAS A FAILED PRODUCT THEY SUBMITTED TO FDA FOR APPROVAL.
They took the studies of other MNRA vaccines and gave it to the FDA. THESE FAILED - its against the law! The FDA shows evidence of colusion with the manufacturer / Moderna.
This package also contained 3 different modules, and 3 different versions. Thats unheard of. Why were there 3 different modules and versions?
Which one did the FDA use - it's a matter of law.
One had a 5 mg. Spike protein, the other had 20 mg. Spike protein and completely different formulas. You can't study something this way. It needs to be exactly the same. You must prove the same result- not with multiple versions. Even summary documents are different versions.
They took the studies of other MNRA vaccines and gave it to the FDA.
Sasha then points out that the MRNA is the carrier for the "payload" (which is the Spike protein/ active ingredient) which would be reactive to the immune system.
They didnt study the active ingredient, the Spike protein. There were NO TOXICITY STUDIES IN SPIKE PROTEINS, which is what is harming people.
They want you to believe if you have a truck filled with food or a truck filled with explosives, they would do the same amount of damage. Obviously that is preposterous. As a new molecular entity you are required to study a new molecular entity, both the truck and whats inside the truck. The vehicle and payload. Both separately and together. This is required by law.
FDA needs to do toxicity studies when approving any new product.
Does it kill, maim, cause cancer, what are the short term effects, what are the long term effects, is it mutinogenic, does it cause fetal damage, what impacts are there on a control group vs. a non control group? Etc.!!
They did 1 study which wasn't finished on rats / which you can't draw any conclusions from.
Of the 29 studies offered, NONE PROVED LEGIT ALL USED FLAWED LABORATORY PRACTICES.
Only 1 looked at toxicity, but it was never completed.
They used these studies for approval, and when they give horrendous safety signals, they say they are illegitimate
THEY USE DECEPTIVE LANGUAGE, - NO VAX RELATED DEATHS, - BUT THERE WERE DEATHS. THEY JUST LIED AND TERMINATED THE STUDY.
They are dismissing their own findings
They say in one sentence they have no mouse adapted virus, yet in the next sentence they say Ralph Baric gave us a mouse adapted virus.
RFK says lets talk about conflicts of interest.
Sasha said the whole time-line doesnt make any sense.
Non clinical vs. pre - clinical/
What was done after clinical trials in humans is a major safety violation.
She was also looking at the Summary Basis For Regulatory Action Documents
Moderna 1st section had a pre I N D (Investigational New
Drug) meeting with the FDA on Feb. 19 2020 and the NEXT day had an IND OPEN.
March 11 the pandemic was declared. These visionaries could forsee the future and have a vaccine in the making prior to outbreak.
So a genomic sequence they had by Jan. 9
There were also 2 applications.
There is only ever one.
The one application (owenership) was the NIH, under Fauci, which was used on Feb. 20th to open IND. And another for Moderna as a commercial and legal (ownership). So the relationship between the NIH, (WHICH TAKES TAX PAYER MONEY FOR FUNDING), and the manufacturer goes way beyond a patent deal.
Collecting royalties and lying to the public about safety and conflicts of interests are serious violations.
Moderna was always a well funded failure.
They used Zika vaccine for approval financed by Fauci, which showed it created ADE. It proved those who got vaccinated were more likely to get the vaccine then those who didn't.
THE ANIMALS ALL DIED WHICH GOT VAXXED, and when restructured the best outcome was 20% died.
NIH, MODERNA, AND THE FDA ALL KNEW ABOUT THIS BEFORE THE APPROVAL
These same people that force everyone to take these vaccines; universities, military, mothers, and now children are the ones profiting from, and lying to you to do so.
A PERFECT CARTEL ARRANGEMENT
The papers also show fertility and reproductive issues. The pre clinical trials showed vaxxed related injuries and toxicity through Modernas own studies. They even state that these are vax related, weight loss, hair loss, skeletal malformations, nodules during development, abnormalities in baby.
The coercion to vaccinate pregnant woman was something I'd never seen. There were commercials, they were told it's safe, and you NEVER give an experimental drugs to pregnant women, let alone children.
The FDA sees this and still tells the public there are no abnormalities, no defects related to the vaccine, when its in the study approved by them and given to them by Moderna.
Then Moderna lies like a rug and says there are no related abnormalities, or alarming findings.
Now what they are doing to the children.
The FDA sat on this information for over a year, and I only got it through a court order.
Lets pray this death cartel ends soon.
https://live.childrenshealthdefense.org/shows/the-defender-show/DDCPPoqCcJ