Sunday, December 15, 2024

EU Committee Gives Green Light To Use 'Self-Replicating' mRNA Vaccines


European Committee gives green light to use self-replicating vaccines on citizens of EU countries



The Committee for Medicinal Products for Human Use has recommended marketing authorisation for Kostaive, a self-replicating mRNA (“saRNA”) injection developed by Arcturus Therapeutics.  The final decision for regulatory approval now rests with the European Commission.

The European Commission must reject authorisation for these dangerous saRNA (replicon) vaccines.


Covid-19 Self-Amplifying mRNA Injection Nears European Approval

By Nicolas Hulscher as published by Courageous Discourse

On 12 December 2024, the European Committee for Medicinal Products for Human Use (“CHMP”) issued a positive opinion recommending marketing authorisation for Kostaive, a self-replicating (replicon) mRNA injection developed by Arcturus Therapeutics. The final decision for regulatory approval now rests with the European Commission:

Here’s a visual representation of how these dangerous genetic shots work:



Japan had already approved these injections last year. In November 2023, Japan’s Ministry of Health, Labor and Welfare (MHLW) fully approved CSL and Arcturus Therapeutics’ replicon shot, Kostaive ARCT-154. Despite enormous safety concerns, Japan’s MHLW approved the updated booster shot in September 2024 to target the JN.1 lineage of Omicron subvariants.

During the clinical trials for Kostaivefive deaths were reported among participants in the phase 3b study. Across study phases 1, 2, and 3a combined, 90% of injected participants experienced adverse events, with 74.5% reporting systemic reactions and 15.2% requiring medical attention after the first dose. Notably, many of the study authors are full-time employees of Arcturus Therapeutics, raising concerns about bias in their conclusions.


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 All self-amplifying mRNA injections currently available for humans and animals should be immediately withdrawn until comprehensive, long-term safety studies are conducted.

Attack of the Replicons, Courageous Discourse, 7 November 2024


Notice of Extreme Concern sent to 10 European heads of government demanding covid mRNA “vaccines” be immediately halted

Rhoda Wilson


The UK has joined nine other countries in the NORTH Group who are writing to the Prime Ministers of their countries to express extreme concern about the safety and quality of covid mRNA vaccines, citing excessive levels of residual DNA found in samples from Australia, France, Germany, Canada, and the USA.

The notice is signed by several prominent UK figures.  The group is demanding an immediate halt to the use of covid mRNA vaccines, a product recall, an independent and transparent investigation into their approval and use, and scientific evidence that documents no risk of damage to human DNA.

The NORTH Group is a growing coalition of engaged citizens from countries throughout Northern Europe. Its aim is to raise awareness about the potential harms posed by modified mRNA therapeutics.  One of its initiatives is a “notice of extreme concern” being sent to the heads of government in countries that have joined the coalition.  This notice was sent to UK Prime Minister Keir Starmer and 9 other European leaders on Tuesday.

The “notice of extreme concern” sent to Starmer was dated 25 November and signed by medical professionals from various fields. It highlights concerns about the excessive levels of residual DNA identified in Australian samples, which confirmed previous data from France, Germany, Canada and the USA.

The introduction of foreign DNA into cells via lipid nanoparticles may cause genomic instability, cancer and other serious conditions, prompting the group to call for the immediate suspension of these vaccines.


“[There are] unquantified risks for human health that have been systematically avoided by the regulatory authorities charged with their oversight,” the notice states. “Therefore, on behalf of the public we call for:

  • An immediate halt to the use of covid-19 modified mRNA vaccines and a product recall;
  • An independent and transparent investigation into their approval and use;
  • Scientific evidence that documents that there is absolutely no risk of damage to human DNA.”

The notice urges Starmer to act in the interest of the country’s citizens and address the scientifically supported threat to current human health and that of future generations.

The 91 UK signatories include general practitioners, consultants, surgeons, researchers and other medical professionals, both retired and practising, with diverse specialisations such as cardiology, rheumatology, ear, nose and throat, ophthalmology and occupational health.

The notice was sent to the leaders of 10 northern European countries on 10 December.  You can read the notice of concern, and find the references cited and a list of the UK signatories and references cited HERE. All the international signatures to the letter are available on the NORTH Group’s website HERE.



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