Attack of the Replicons
The Biopharmaceutical Complex’s self-amplifying mRNA assault has already begun
By Nicolas Hulscher, MPH | Courageous Discourse | November 7, 2024
The Biopharmaceutical Complex is preparing for the large-scale deployment of replicon (self-amplifying) mRNA injections. There are currently at least 33 candidates in development.
These products behave like a synthetic virus. The replicon mRNA is designed to encode not only the target antigen but also viral replicase, enabling the mRNA to replicate itself within the target cells. This replication machinery allows for an unknown period of toxic antigen production. Concerningly, none of the clinical trials have addressed the major concern of product shedding.
The Coalition for Epidemic Preparedness Innovations (CEPI) and the Biomedical Advanced Research and Development Authority (BARDA) are the primary funders behind this technology to combat ‘Disease X’. This is an extremely high risk ‘vaccine’ platform that should be avoided at all costs. Cellular installation of synthetic replicons requires decades of intense safety testing.
The very first replicon injection for human use received emergency use authorization (EUA) from The Office of the Drugs Controller General of India (DCGI) back in June 2022: Gennova Biopharmaceuticals’ GEMCOVAC-19. This was followed by reckless EUA approval in June 2023 for GEMCOVAC-OM, a replicon booster shot that targets the Omicron strain.
In November 2023, Japan’s Ministry of Health, Labor and Welfare (MHLW) fully approved CSL and Arcturus Therapeutics’ replicon shot: KOSTAIVE ARCT-154. Dismissing all concerns, Japan’s MHLW approved the updated booster shot in September 2024 to target the JN.1 lineage of Omicron subvariants.
In the clinical trials for ARCT-154, 5 deaths occurred among the injected in study phase 3b. Injected participants experienced a 90% adverse event rate (74.5% systemic – 15.2% required medical attention) after the first dose in study phases 1, 2, and 3a combined. Many of the authors are full time employees of Arcturus Therapeutics, meaning their conclusions are likely biased.
Meanwhile, the USDA quietly approved an experimental self-amplifying RNA injection for dogs developed by Merck in June 2024: Nobivac NXT Canine Flu H3N2. It appears that Merck is attempting to camouflage the fact that this product is self-amplifying. The primary product description only indicates that it uses “revolutionary RNA particle technology.” However, the novel platform works by RNA particles targeting dendritic cells, where they self-replicate and result in sustained antigen production.
The possibility of product shedding from dogs to humans or other animals was never tested. This injection is currently widely available for online purchase and canine administration. While the Biopharmaceutical Complex struggles to get self-amplifying mRNA injections approved for humans, they seem to have no problem targeting our pets.
Deployment of this experimental platform has continued in September 2024 to target cats: Nobivac NXT FeLV. Nowhere in the product brochure does it mention the RNA self-amplification mechanism of action. They hope that unsuspecting vets won’t think twice about accepting the ‘new and improved’ product. The so-called ‘safety’ data for this product is as follows:
“Demonstrated safety under field conditions” from “Data on file. Merck Animal Health.”
In other words, no public safety data is provided. It’s become abundantly clear that the pharmaceutical industry and captured regulatory agencies have zero regard for the massive safety concerns of undefined synthetic mRNA replication resulting in uncontrolled toxic antigen production. These experimental injections must not receive further regulatory approval for humans or animals if we are to prevent another public health disaster. All self-amplifying mRNA injections currently available for humans and animals should be immediately withdrawn until comprehensive, long-term safety studies are conducted.
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From the Archives
Murdering Babies is “Permissible” When They’re Palestinian
What the Media Missed on Itamar
By ALISON WEIR | CounterPunch | March 17, 2011
US media have been widely and repeatedly reporting on the awful March 11 murder of three small Israeli children and their parents. While no one yet knows who committed this act, reports presume that the murderers were Palestinian, and for this reason the incident is receiving major attention. Various heads of state, including President Obama, have condemned it.
If it turns out that the murderer or murderers were Israeli, as some previously presumed “terrorists” have turned out to be, or a foreign worker who had previously threatened the family over unpaid wages, as some reports from the area suggest, it is likely that coverage of the incident will quickly vanish from U.S. headlines.
For now, however, American news reports continue to provide excruciating details about the atrocity. Given the amount of reportage, it is surprising how much significant information is omitted.
For example, none of these reports mention that the location of the murders, Itamar (near Nablus), is an illegal Jewish-only settlement on stolen Palestinian land in the midst of refugees whom Israel pushed off their ancestral land through massacres and ruthless military actions.
Nor do reports mention the frequency with which Israeli settlers beat, occasionally torture, and sometimes murder Palestinians of all ages, burn their crops, and hack down their groves of olive trees, the livelihood of many Palestinian villagers; hundreds, at least, of these trees, have been destroyed by rampaging Israeli settlers. … continue
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