A world-renowned vaccine expert has presented evidence during congressional testimony showing that pharmaceutical giant Moderna knows its Covid mRNA shots cause cancer.
Dr. Robert Malone, the inventor of mRNA vaccine technology, testified during a hearing on Capitol Hill led by Republican Rep. Marjorie Taylor Greene (R-GA).
During his testimony, Malone presented the patent for Moderna’s Covid vaccine.
Moderna’s patent shows that its COVID-19 vaccine vials contain billions of DNA fragments.
Those fragments, along with other contaminants, are linked to birth defects and cancer.
In the patent, Moderna admits that contaminants in the shots cause cancer.
However, as Malone highlights in his testimony, the U.S. Food and Drug Administration (FDA) apparently ignored this admission when approving the shots for public use.
The failure raises major concerns, especially as several top FDA officials secured high-paying jobs with Moderna after they approved the injections, as Slay News reported.
During the hearing, Dr. Malone highlighted that Moderna acknowledges in its patent that RNA is preferable to DNA in vaccines.
RNA is preferred due to the risks involved, Malone explains.
Yet despite the risks, Moderna’s mRNA injection is contaminated with billions of fragments of DNA.
“Moderna has a patent on the use of RNA for vaccines,” Malone told the hearing.
“And in that, Moderna explicitly acknowledges that RNA is superior to DNA for vaccine purposes because of problems, including the possibility of insertional mutagenesis that could lead to the activation of oncogenes or the inactivation of tumor suppressor genes.
“FDA says they’re not aware of any concerns, but Moderna in its own patent lays out exactly the same concerns that exist about DNA in insertional mutagenesis and genotoxicity.
“So, Moderna knows it – DNA is a contaminant.
“It is left in because of the way they make it … they use DNA to make RNA, and then they degrade the DNA, and then they have to purify the degraded DNA away from the RNA.
“And the process they are using is apparently not that good.”
WATCH:
Moderna ADMITS That DNA Contamination Can Lead to Cancer
• Moderna has a patent that acknowledges RNA is preferable to DNA in vaccines due to risks of insertional mutagenesis, which might activate oncogenes or inhibit tumor suppressor genes, Dr. @RWMaloneMD explained.
• A new… pic.twitter.com/EEAybZgrRZ
— The Vigilant Fox 🦊 (@VigilantFox) November 15, 2023
A new preprint study up for peer review has found billions of residual DNA fragments in COVID-19 mRNA vaccine vials.
The lead author of the study, molecular virologist David Speicher, who has a doctorate in virology, told The Epoch Times that the study is “the largest study” on residual DNA in COVID-19 vaccines to date.
“In our study, we measured DNA copies of spike, ori (origin of replication), and SV40 enhancer genes,” he told the outlet.
“The loads of SV40 enhancer-promoter, ori, and virus spike in Pfizer are up to 186 billion copies per dose.”
The spike he refers to is the DNA sequence of the SARS-CoV-2 spike protein, which can be transcribed to spike mRNA to be used in the COVID-19 mRNA vaccines.
The other two DNAs—SV40 enhancer genes and ori—help facilitate the replication of spike DNA.
However, the final mRNA vaccines should only include RNA and not residual DNA instructions for spike production.
The researchers sequenced the gene material in 27 mRNA vaccine vials from 12 different lots.
Nineteen vials were from Moderna, and eight were from Pfizer.
The documentation for Moderna’s patent suggests that there are certain DNA sequences present in the vials that are normally not allowed in anything that is going to go into humans, “not the least of which is an antibiotic resistance gene,” Malone explained.
“They include these sequences from Simian Virus 40 – not the whole virus, but highly active promoter sequences – which is exactly the thing that the FDA in their older regulations said must be avoided because it confers even more risk for insertional mutagenesis.”
Meanwhile, the study found that Pfizer’s Covid mRNA injection also contains the same contaminants.
Documentation was provided by the company to regulators in the U.S., Europe, and Canada.
According to Malone, these regulators removed the notation about SV40 sequences.
The removal of the information appears to be an apparent attempt to hide it from the public.
“The FDA didn’t take the raw DNA sequences, reconstruct those plasmid maps, and look at them themselves,” Malone clarifies.
“They just took for granted what Pfizer had given them.
“And now this is all coming out because of what these researchers found.”
Malone argues that executives and scientists at Moderna and Pfizer must have known about the risks.
Dr. Malone warned that those who have received the mRNA injections would likely be at risk from “anything that is associated with DNA damage.”
In terms of DNA damage, Malone explains that “birth defects and cancer [are] the most notable ones.”
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