FDA defies RFK Approving Dangerous Moderna’s Next-Gen COVID mRNA Vaccine. US MD: “It’s the CANCEROGENIC Self-Amplifying RNA shot”
by Fabio Giuseppe Carlo Carisio
The latest articles published by the most authoritative American medical bloggers are destined to stir up a huge hornet’s nest all over the world for various reasons:
FDA (Food and Drug Administration) and CDC (Centers for Disease Control and Prevention), the highest government health authorities in the USA, seem to want to continue to support Big Pharma by ignoring the requests for safety checks by lawyer Robert F. Kennedy Jr., who went from being a NO-VAX activist to Secretary of the Department of Health in the Trump administration
- FDA has approved Moderna’s new generation vaccine mNEXSPIKE without specifying whether it is of the self-replicating samRNA type whose dangerousness was denounced by investigations by Gospa News and by some Italian doctors. According to the authoritative pharmaceutic researcher Sahasha Latypova, may be precisely that…
- But a few hours after our article also the famous American cardiologist Peter McCullough and epidemiologist Nicolas Hulsher, who published many study on Covid vaccines, confirmed that are the new damgerous sa-mRNA technology
- In their Substack Courageous discourse they reported the issue with an unequivocal title: “BREAKING: Reverse Transcription, Carcinogenesis, and the mRNA Catastrophe Deepen with FDA Approval of mNEXSPIKE”
- The new mRNA gene serum is declared ready for sale by 2025-2026 as if the new Covid Pandemic announced by WHO and American and Chinese scientists suspected of having built SARS-Cov-2 in a laboratory were already about to happen.
- One of them is Ralph Baric, the trusted microbiologist of virologist Anthony Fauci who worked together with the Pentagon on the Moderna vaccine approved in March 2019, 9 months before the Covid pandemic…
- Moderna’s vaccine is based on the previous pharmaceutical product Spikevax (sponsored by Bill Gates and by 2020 Trump’s Warp Speed plan) which is at the center of some global investigations for its dangerousness and of various lawsuits for the vaccinated killed and damaged…
- The CDC has not yet adopted on its official website the indications announced by RFK jr to no longer recommend mRNA gene serums to pregnant women and children…
The suspicion is starting to grow that President Donald Trump, abandoned by Elon Musk, Bill Gates’ only enemy, is giving in to the flattery of Big Pharma who had dinner with him just after his electoral success in November 2024.
FDA has approved new Moderna Covid shot without Placebo Controlled trials
«It just approved Moderna’s newest COVID-19 mRNA shot—mNEXSPIKE—without a single placebo-controlled trial, directly contradicting recent public assurances from HHS that “all new vaccines will undergo safety testing in placebo-controlled trials prior to licensure.».
The famous American Epidemiologist Nicolas Hulsher has pointed out today in his Substack…
However, this authorization appears to align with their so-called “evidence-based approach to COVID-19 vaccination” published in NEJM —a policy that permits the continuation of mass experimentation on many Americans without clinical proof of benefit, Hulsher added.
According to Moderna:
The U.S. Food and Drug Administration (FDA) has approved mNEXSPIKE® (mRNA-1283), a new vaccine against COVID-19, for use in all adults 65 and older, as well as individuals aged 12-64 years with at least one or more underlying risk factor as defined by the Centers for Disease Control and Prevention (CDC).
The company said it expects to have the vaccine, called mNEXSPIKE, available for the 2025-2026 respiratory virus season. “The FDA approval of our third product, mNEXSPIKE, adds an important new tool to help protect people at high risk of severe disease from COVID-19,” CEO Stephane Bancel said in the statement.
Pharma Researcher Latypova warns: “Moderna Carefully omits that is a self-amplying RNA Shot”
«Quoting from Moderna’s press release, which carefully omits mentioning that this is a self-amplifying RNA shot», according to famous investigative blogger Sasha Latypova, for many years a pharma and medical device R&D executive.
The approval was based on an 11,400-person trial that tested the new shot against its older product, to determine whether it was at least as effective, according to the company. The ongoing Phase 3 clinical trial (ClinicalTrials.gov Identifier: NCT05815498) is a randomized, observer-blind, active-controlled study of approximately 11,400 individuals aged 12 years and older. Half of the participants received a 10 μg dose of mRNA-1283, while the other half received a 50 μg dose of mRNA-1273 (Spikevax).
«This gets very interesting for several reasons I would like to repeat that this clinical trial had NO PLACEBO CONTROL! Please, all MAHA-mates – note that this trial is fully compliant with the current, brand new MAHA-FDA policy by Makary & Prasad: there is no requirement for a placebo-controlled trial before the approval of new versions of mRNA, even radically new versions like this self-amplifying RNA shot» Latypova added.
There is some confusion as to whether this version of Moderna shot is “self-amplifying”. We are going to FOIA the FDA to get the exact information, she pointed out in her Substack. At this time, the vax is described as:
Moderna’s candidate, mRNA-1283, is one-fifth the dose of the first-generation Spikevax, accomplished by replicating specific regions of the virus’ protein as opposed to the entire thing. The company has said that the specific regions, the receptor-binding domain and the N-terminal domain, have shown to be critical to eliciting neutralizing antibodies.
«Given the statement about 1/5 of the dose and replication of specific regions, I am inclined to think it is self-replicating, but will confirm once we get better information» Latypova concluded.
McCollough: “DNA Altered from mNEXSPIKE utilizing self-amplifying RNA (saRNA) technology”
«New evidence reveals a troubling reality: synthetic mRNA vaccines are not the safe, transient agents they were claimed to be. Instead, they can undergo reverse transcription, integrate into host DNA, disrupt genomic integrity, and activate oncogenic pathways. This alarming data, emerging from recent transcriptomic analyses, confirms that mRNA technology carries serious carcinogenic risks».
The famous American Cardiologist Peter McCullough worte in his Substack Courageous Discourse (link in the sources)
«At the same time, the FDA’s recent approval of mNEXSPIKE, a vaccine utilizing self-amplifying RNA (saRNA) technology, signals a dangerous escalation. This next-generation platform intensifies human exposure to synthetic RNA and spike proteins, greatly increasing the risk of genomic damage, cancer, and other serious harms».
This is the same extremely dangerous biotechnology used in the Kostaive vaccine recently approved by the European Commission…
Reverse Transcription and Genomic Instability Confirmed
Contrary to early assurances, synthetic mRNA injected into humans is not biologically inert. Dr. John Catanzaro of the UNT Genomics and BioDiscovery Institute and Dr. Peter McCullough have presented compelling evidence that synthetic mRNA can be reverse-transcribed into DNA within human cells.
Their study of tumor tissues from vaccinated patients showed:
- Increased evidence of embedded spike RNA fragments in host genomic data
- Activation of DNA damage response pathways
- Upregulation of oncogenes associated with tumorigenesis
- Aberrant transcriptional activity linked to immune evasion and cellular transformation
Dr. McCullough emphasized the gravity of these findings:
“We now have definitive evidence that the synthetic mRNA platform, as deployed in COVID-19 vaccines, is not biologically inert. It hijacks cellular machinery in a way that risks genomic instability, immune evasion, and even carcinogenesis.”
C.D.C. Contradicts Kennedy and Keeps Advice That Children May Get Covid Shots
Earlier this week Secretary of HHS Robert F. Kennedy Jr., flanked by Dr. Jay Bhattacharya, director of the National Institutes of Health, and Dr. Marty Makary, U.S. Food and Drug Administration commissioner, announced on Musk’s X platform that the CDC was no longer recommending COVID vaccines for healthy children and healthy pregnant women.
«I, along with many others, noticed that while these three men were saying that the CDC was no longer recommending COVID vaccines for these healthy children and pregnant women, the official government CDC website had not changed their recommendations yet» Brian Shilhavy, Editor of Health Impact News has written
«Yesterday, the CDC did update their website regarding recommendations for COVID vaccines, but the recommendations that the three Government health public servants deceivers said would be gone, were still there» Shilhavy highlighted.
From the New York Times:
Health Secretary Robert F. Kennedy Jr. said on Tuesday that the vaccine would no longer appear on the childhood immunization schedule. C.D.C.’s update counters his policy.
Days after Health Secretary Robert F. Kennedy Jr. announced that Covid shots would be removed from the federal immunization schedule for children, the Centers for Disease Control and Prevention issued updated advice that largely countered Mr. Kennedy’s new policy.
FDA Directs COVID-19 Vaccine Big Pharma to Expand HEART INFLAMATION WARNING
The agency kept Covid shots on the schedule for healthy children 6 months to 17 years old, but added a new condition. Children and their caregivers will be able to get the vaccines in consultation with a doctor or provider, which the agency calls “shared decision-making.”
The shots will also remain available under those terms to about 38 million low-income children who rely on the Vaccines for Children program, according to an emailed update from the C.D.C. on Friday.
Fabio Giuseppe Carlo Carisio
director of Gospa News
investigative journalist since 1991
VT columnist since 2019
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