THE #MonkeyBusiness - HOW #BioNTech & #Pfizer LIED ABOUT THEIR PRE-CLINICAL STUDIES, AND HOW HEALTH REGULATORS AND NATURE MAGAZINE WHO "PEER REVIEWED" THEIR STUDY DIDN'T EVEN CARE.

By Ehden Biber

CHAPTER 1 - THE SCHEDULE

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On the 1st of February 2021 @Nature magazine published "BNT162b vaccines protect rhesus macaques from SARS-CoV-2". It was the only article #Pfizer/#BioNTech published in academic literature about their animals pre-clinical experiments.

#MonkeyBusiness
nature.com/articles/s4158…
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The results of the mice and monkeys studies which are mentioned in this article played a CRITICAL role in #BioNTech/#Pfizer Emergency Use Authorization.
I've covered the problematic usage of these animals in my previous thread, #TheRats.
#MonkeyBusiness
4/
Here is the 1st quote from #BioNTech/#Pfizer "Module 2.4. Nonclinical Overview", which covered the monkey studies. If you read #TheRats, you know that the claim highlighted in red is a lie, and that everyone who worked in this field knew it is one.

#MonkeyBusiness
5/
And here are more quotes from #BioNTech/#Pfizer "Module 2.4. Nonclinical Overview" about the monkeys studies.

Looks impressive, doesn't it?

Of course it does.

Sadly, as you are about to find out, it's all fake.

#MonkeyBusiness
6/
Let's go back to the research paper that was published in Nature magazine, which was first submitted by #BioNTech/#Pfizer as a preprint on September 8th, 2020.

This means health regulators had it prior to their EUA approval.

#MonkeyBusiness

doi.org/10.1101/2020.0…
7/
There are A LOT of things that should have alerted the regulators (and those who performed the peer-review for Nature magazine), but in this thread, we will focus on one of them, the schedule of the study according to #BioNTech/#Pfizer, and related results.
#MonkeyBusiness
8/
According to #BioNTech/#Pfizer "Extended Data Figure 6." there were ZERO monkeys who received BNT162b1 30μg.

AND YET IN "Fig. 3: Macaque immunogenicity" THERE ARE RESULTS OF 6 MONKEYS WHO "RECEIVED" BNT162b1 30μg.

Who were these monkeys???

#MonkeyBusiness
9/
According to #BioNTech/#Pfizer "Extended Data Figure 6." there were 3 monkeys who received BNT162b2 30μg, as part of a "sentinel group".
And yet in "Extended Data Fig. 5: Macaque CD4+ and CD8+ T cell response" there are results of 6 monkeys with BNT162b2 30μg.

#MonkeyBusiness
9/
Here is "Extended Data Fig. 8". Notice how day 6 in "Thoracic Radiograph Scores" (Chest X-Ray) is missing scores for the following monkeys:
3 "Sentinel"
6 "control"
6 "BNT162b1"

Why did #BioNTech/#Pfizer decided not to test them on day 6?

#MonkeyBusiness
10/
More on "Extended Data Fig. 8" X-ray. #BioNTech/#Pfizer used a score of 0 to 3 for 7 lung regions, and the "Sentinel" group were not challenged with #SARSCoV2.
Could it be that the 3 monkeys in that group that has higher score in 10/EOP are the BNT162b2 30μg?

#MonkeyBusiness
11/
"Extended Data Fig. 8" also covered chest CT scores.
How come the "Sentinel" group only shows scores to 3 monkeys, not 6? How come Pulmonary Histopathology is missing for the sentinel group? Was #BioNTech/#Pfizer trying to hide something?

#MonkeyBusiness
12/
According to #BioNTech/#Pfizer, "The three control macaques in challenge cohort 3 and three sentinel macaques were not necropsied to allow their subsequent rechallenge (control) or challenge (sentinel)". Rechallenge to what? Challenge to what?
What's going on?
#MonkeyBusiness
13/
More questions:
1) Why did #BioNTech/#Pfizer created a sentinel group?
2) Why was there no autopsy for the 3 BNT162b2 30μg monkeys?
3) WHO THE HELL REVIEWED THIS RESEARCH PRIOR TO EUA AND APPROVED IT?
4) WHO THE HELL APPROVED TO PUBLISH IT IN NATURE MAGAZINE?

#MonkeyBusiness
14/
As I wrote before, this #BioNTech/#Pfizer "safe and effective" #MonkeyBusiness is bigger than just the suspicious study design ("Sentinel"), fake and missing information, and weird schedule. THESE RED FLAGS ARE JUST A TIP OF THE ICEBERG.

STAY TUNED FOR MORE, SOON!
15/
[UPDATE]

I'VE JUST PUBLISHED CHAPTER 2 OF #MonkeyBusiness.

I CALLED IT "THE PREPRINT".

PLEASE MAKE SURE YOU DO NOT MISS IT, AND PLEASE SHARE THE THREADS !!!

#BioNTech/#Pfizer
#StoptheShotsNow

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More from @eh_den

May 14
Pediatric Moratorium! Adult Use Restrictions! Veterinary Prohibition!
"Codon Optimization in mRNA Vaccines and Gene Therapies: An Assessment of Protein Misfolding Risks and Regulatory Oversight" submitted to the FDA's Vaccines and Related Biological Products Advisory Committee!
Here's the Executive Summary

Objective: This white paper evaluates the scientific evidence and regulatory oversight related to codon optimization in messenger RNA (mRNA) vaccines and gene therapies for both human and animal applications. Its primary goal is to assess whether the potential risks—specifically protein misfolding, aggregation, and associated diseases like amyloidogenesis and prionogenesis—justify a moratorium on this technology’s use. The analysis aims to inform policy by balancing innovation with safety.

Scope: The assessment covers the principles of codon optimization, the mechanisms of protein folding and misfolding during translation, and the risks of amyloid formation and prion-like propagation. It reviews regulatory frameworks, including the U.S. Food and Drug Administration (FDA) and European Medicines Agency (EMA) Chemistry, Manufacturing, and Controls (CMC) requirements. The scope includes a detailed examination of scientific literature—both foundational and recent—such as studies on tissue-specific codon usage, codon context effects, and structural risks in mRNA vaccines. It also analyzes preclinical and clinical safety data, pharmacovigilance reports, and a case study on COVID-19 mRNA vaccines. Additionally, the paper explores implications for veterinary vaccines and food chain safety, concluding with an updated risk management and policy evaluation.

Key Findings: Codon optimization enhances protein production in mRNA-based vaccines and therapies but introduces risks that challenge its presumed safety. New research shows that changing codons—previously thought to be neutral—affects translation speed and accuracy, potentially leading to protein misfolding and aggregation. For example, the cardiomyocyte PAO model reveals that misfolded proteins can cause delayed, severe damage, such as heart failure, broadening concerns beyond brain-related diseases. Data from TissueCoCoPUTs indicate that generic codon optimization often mismatches the translation needs of specific tissues, increasing misfolding risks. In COVID-19 mRNA vaccines, structural issues like excessive G-quadruplex formation may heighten these dangers.
Regulatory oversight, however, falls short. There are no standard tests to evaluate how codon changes affect protein shape or clumping, and long-term monitoring is insufficient to detect slow-developing issues like neurodegeneration or prion-like diseases. The rapid rollout of COVID-19 mRNA vaccines lacked thorough evaluation of these folding risks. In veterinary applications, the use of codon-optimized therapies in livestock raises unresolved concerns about misfolded proteins entering the food chain and environment, potentially affecting human health.

Conclusion on Moratorium
Given the mounting evidence of risk and gaps in oversight, a tiered moratorium is recommended as the most cautious and effective approach:

· Pediatric Moratorium: Codon-optimized mRNA vaccines and gene therapies should not be used in children under 18 until safer practices are developed. This includes using tissue-specific codon designs, conducting 24-month safety studies in primates, and setting limits on G-quadruplex formation. Children’s developing tissues are especially vulnerable, and long-term data are lacking.

· Adult Use Restrictions: New clinical trials for risky mRNA designs—those with heavy optimization, high clumping potential, or rich GC content—should pause. This halt would last until advanced tests, such as Kinetic Folding Assurance (KFA), hidden gene screening, and cross-seeding checks, are required.

· Veterinary Prohibition: Codon-optimized gene therapies in animals entering the food supply should be banned. Evidence from the PAO model and prion diseases suggests a risk of transmissible misfolded proteins, posing a threat to food safety.

This moratorium should persist until:
· Reliable tests for protein folding and clumping are part of regulatory standards.
· Codon optimization accounts for tissue-specific needs and translation timing.
· Independent research verifies the safety of high-risk designs and pediatric use.
· Better monitoring systems track long-term health effects.

This approach marks a shift in how codon optimization is viewed: it’s not just a tool for efficiency but a process that demands careful study of its effects on protein structure and safety over time. By adopting these measures, we can protect public health while still advancing mRNA and gene therapy innovations.Image
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The whitepaper has just been published in my Sub/I\Stack (Link in my pro/I\file)!
I published my first article on codon optimization risks and the COVID-19 vaccine in August 2021 (#COptiGate) and wrote extensively on the topic. This white paper, submitted to the @US_FDA, is my final attempt to highlight our regulators' complete failure.
Read 4 tweets
Apr 7
🚨Microwave Ovens Might Be Risking Your Health! 🚨
Did you know that eating microwaved food could cause blood changes linked to cancer? Russians knew it. Swiss scientist Dr. Hans-Urich Hertel discovered this over 30 years ago, but the microwave industry tried to silence him.
🧵 Image
Dr. Hans-Urich Hertel was a Swiss food scientist who challenged microwave safety. In 1989, he teamed up with Professor Bernard Blanc to study how microwaved food affects us. Their findings? Alarming enough to spark a decade-long battle! #ScienceHeroes #MicrowaveResearch
Hertel and Blanc recruited eight volunteers from a macrobiotic institute in Switzerland. For eight weeks, they ate raw, conventionally cooked, or microwaved foods—like milk and veggies—under strict conditions (no smoking, alcohol, or sex!). Blood tests followed every meal. #MicrowaveStudy #HealthResearch
Read 22 tweets
Jul 20, 2024
THE GLOBAL IT OUTAGE YOU WITNESSED WAS NOT AN ACCIDENT!
IMPORTANT! The purpose of this thread is to explain non-IT and to non information/cyber security professionals why I believe the outage you are seeing around the world due to the update from #Crowdstrike is not an accident.
Before we begin - introduction.
Hi everyone. My name is Ehden Biber. I'm known as the person behind #PfizerLeak, and most of my writing here on X/Twitter has been on ph@rma related topics. HOWEVER, my professional work has been information security and cybersecurity.
My credentials include:
· Head of information security in Metro Bank (UK).
· Merck/MSD Information security office for Europe, Middle East and Africa (EMEA).
· Consultant to insurance and financial institutes.

The opinion you are about to read is based on YEARS of experience.
Read 41 tweets
Jun 3, 2024
"MEDICAL GENETICS…WILL BE THE SOUL OF PERCISION MEDICINE IN EVERY FIELD"
It is time to expose another member of the W.H.O. science council and her views on genomics and gene therapy (mRNA). Introducing Dr Mary-Claire King.

[Thread]
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Doctor Mary-Claire King is a very known geneticist who has discovered in 1990 BRCA1,which was the first gene for a hereditary form of breast cancer. She is a professor of genome sciences in the university of Washington, Seattle, USA.
medgen.uw.edu/people/mary-cl…
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Her later work was focused on the genetics of schizophrenia, she is recognized as a pioneer in the development of DNA sequencing for human rights investigations, and she is also a Senior Associate Core Member of the New York Genome Center.

nygenome.org/news-events/ne…
Image
Read 7 tweets
May 28, 2024
THE COUNCIL: INTRODUCING THE W.H.O. SCIENCE COUNCIL THAT IS ABOUT TO CONTROL YOUR LIFE.
As we approach the final stages of the #WHO coup d'état attempt, it is time to expose the group of unelected people who will control your future and their alarming agenda!
#TheCouncil
[Thread] Image
2/
In December 2023 the WHO produced a report that sets the stage to radical changes that soon will be enforced all the citizens of the world: make gene therapy (mRNA) key technology in the fight against infectious diseases, cancer, and combat any resistance to such technologies. Image
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It called to develop new gene therapy treatments against pathogens, promote investment in "equitable" development of the technology, use it as THE medical countermeasure mechanism to tackle pandemic threats, and to combat any resistance to the technology ("misinformation").

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Read 43 tweets
May 18, 2024
@robinmonotti 1) He uses the exaggerated Hamas dataset.
2) He uses a definition of children for anyone under 18 years old.
3) He say Palestinians were expelled in 1948, but don't mention many left because Arab nations told them to so they can butcher Jews in the war they started.
More below.
@robinmonotti 4) He compare the number of children who died to the sum total of children died 3 years before. He does not compare it to the number of children who died in other conflicts IN THE REGION, such as in Syria. That like comparing apples and pears.
More below.
@robinmonotti 5) The definition of who is a Palestinian by the UN is ANYONE WHO LIVED IN THE MANDATED PALESTINE FOR TWO YEARS prior to June 1848! No ancestors required!
This also made Egyptians who escaped Egypt not to become work slave in the creation of the Suez canal into Palestinians. Image
Read 4 tweets

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