Moderna Vaccine Patented 9 Months Before Pandemic

That is 9 months before the official outbreak of the Covid-19 pandemic in China and the availability of the official Wuhan sequence MN908947.1, the virus initially called 2019-nCoV and then renamed by the World Health Organization SARS-Cov-2 to the strong genomic identity with SARS of 2003 (Severe Acute Respiratory Syndrome, or Severe Acute Respiratory Syndrome, when virus and disease were called the same).

This revelation comes from “The Fauci / COVID-19 Dossier” prepared by the American doctor David E. Martin who has developed a colossal study on US government-funded patents in relation to Coronaviruses since 2000, so much so that he suspects that SARS too in 2003 was built in the laboratory by microbiologist Ralph Baric of the Chapel Hill research center of the University of North Carolina (UNC) under the aegis of Fauci himself.

As we will see after long but inevitable premises, the registration of Moderna’s experimental vaccine on March 28, 2019 is also confirmed by the official history stored in the patent …

The discovery becomes even more disturbing in light of the fact that such research was conducted by the pharmaceutical company at the same time as Baric’s extremely dangerous experiments on SARS recombinant viruses conducted together with the director of the Infectious Diseases Research Center of the Wuhan Institute of Virology, Shi Zhengli, not randomly dubbed in China “BatWoman” for its coronavirus tests of horseshoe bats.

As anticipated before the online investigation in the book WuhanGates (December 2020), they would be the godfathers and progenitors of a huge plot of the New World Order of ancient British Masonic origin hatched under the sign of the Chinese Communists and American Democrats.

To it were also added the peremptory paws of Italy and Saudi Arabia aimed at global immunization projects preparatory to the health dictatorship of the Covid-19 emergency and the promotion of experimental anti-Covid gene serums for the enrichment of Big Pharma and speculation of the same investment funds that control the Weapons Lobby.

THE THERAPY OF DONNO AFFOSSED BY THE MODERNA GROUP

Before briefly summarizing the many information contained in the WuhanGates 40 report on the researches of Professor Baric and Doctor Fauci, coordinator of all the most risky and secret experiments on viruses and bacteriological weapons in the 28 American civil and military laboratories as evidenced by the exclusive investigation by Gospa News, we recall another of the mysteries in the ambiguous fight against Covid-19 revealed only by our online newspaper.

Moderna is part of that colossal international Zacks group that became interested in the highly effective therapy against Covid-19 of hyperimmune plasma developed by Professor Giuseppe De Donno and mysteriously vanished in the maze of health policy before his mysterious suicide.

It should also be remembered that the experimental gene sera were able to obtain emergency authorization in the USA, from the Food and Drug Administration which, however, in recent weeks gave definitive ok to Spikevax after having granted it to Comirnaty of Pizer-Biontech amid a thousand controversies for not having subjected the clinical data to the scrutiny of the independent Advisory Committee, and in the European Union by the European Medicines Agency (where they remain with a conditional marketing authorization as still experimental) only by virtue of two factors.

The pandemic has resulted in millions of deaths in the world with Covid-19 (in the minority died from Covid-19 and in the majority from complications of other diseases), in Italy and in other countries mainly due to inadequate home and hospital care such as the betrayal. use of cortisone or the disputed hydroxychlorichine (adopted by the protocols of the Piedmont Region) and the absence of drugs recognized as effective.

Therefore, the stop of the De Donno therapy, successfully carried out in over one hundred American university hospitals as recalled by the Johns Hopkins University in its defense, represented one of the obstacles in alternative treatments functional to the promotion of Moderna and other Big Pharma’s anti-Covid vaccines.

EXPERIMENTS ON CHIMERIC VIRUSES BEFORE 2003

«The National Institute of Health’s grant AI23946-08 issued to Dr. Ralph Baric at the University of North Carolina at Chapel Hill (officially classified as affiliated with Dr. Anthony Fauci’s NIAID by at least 2003) began the work on synthetically altering the Coronaviridae (the coronavirus family) for the express purpose of general research, pathogenic enhancement, detection, manipulation, and potential therapeutic interventions targeting the same. As early as May 21, 2000, Dr. Baric and UNC sought to patent critical sections of the coronavirus family for their commercial benefit».

As Martin’s dossier reports, in one of several articles derived from the work sponsored by this grant, «Baric published what he reported to be the SARS CoV full-length cDNA in which it was clearly stated that SAR CoV was based on a compound. of DNA segments».

«Using a panel of contiguous cDNAs that span the entire genome, we have assembled a full-length cDNA of the SARS-CoV Urbani strain, and have rescued molecularly cloned SARS viruses (infectious clone SARS-CoV) that contained the expected marker mutations inserted into the component clones».

SARS-Cov of 2003 was indicated with the name of Carlo Urbani, the researcher who was analyzing all its characteristics and died prematurely, struck down by the respiratory syndrome, like other scientists who died mysteriously while working on chimeric virus tests (Franc Plummer in Canada ) or when they tried to investigate the origin of these viruses and the gene sera then placed on the market after SARS-Cov-2 (Franco Trinca and Domenico Biscardi and finally the elderly Luc Montagnier).

For the sake of brevity, let’s skip all the references to the patents already mentioned in WuhanGates 40 and come to the conclusions of “The Fauci / Covid-19 Dossier” published by Dr. Martin: «In short, the U.S. Department of Health and Human Services was involved in the funding of amplifying the infectious nature of coronavirus between 1999 and 2002 before SARS was ever detected in humans».

The allusion to the virus that killed the Italian scientist Urbani intent on studying it is very heavy: even SARS 2003 could have been created in the laboratory!

The National Institutes of Health, Allergy and Infectious Diseases worked on SARS Reverse Genetics. study AI059136-01. $1.7 million total costs, RS Baric, PI. 10 percent effort. 4/1/04- 3/31/09. The project develops a SARS-CoV full length infectious cDNA, the development of SARS-CoV replicon particles expressing heterologous genes, and seeks to adapt SARS-CoV to mice, producing a pathogenic mouse model for SARS-CoV infection. Then, subsequently, the same NIAID carries out the research Remodeling the SARS Coronavirus Genome Regulatory Network. RS Baric, PI 10 percent effort. 7/1/04-6/30/09. $2.1 million.

On November 22, 2004, the University of Hong Kong patents the spike protein associated with SARS on CoV and pursues US patent 7,491,489. But on June 2005 also the Pentagon’s DARPA (Defense Advanced Research Projects Agency) gets in on the game Synthetic Coronaviruses with the event Biohacking: Biological Warfare Enabling Technologies, organized in Washington, DC. and sponsored by DARPA/MITRE.

In 2008, funding for Biodefense Grant U54 AI057157 commences with $10,189,682 to UNC Chapel Hill. Where, in the laboratories of North Carolina University, the experiments on chimeric superviruses will be carried out between 2014 and 2017, conducted in spite of Barack Obama’s moratorium on gains in function. And in 2010 the “Biodefense Grant U54 AI057157” continues with $ 8,747,142 to UNC Chapel Hill (non-competitive grant from NIAID). Patent issuance for the SARS coronavirus patents peaked after the outbreak in Asia with 391 patents issued.

We are talking about research funded by DARPA and the Pentagon precisely because they are dedicated to the construction of recombinant viruses, especially SARS infected with HIV as happened with the plasmids built by the Wuhan Institute of Virology thanks to a funding from the European Commission chaired by Romano Prodi, with an increase in the charge. viral through the extremely dangerous Gain of Function technique and with “dual use” purposes, i.e. vaccine but also a military bacteriological weapon: as is the SARS-Cov-2 according to a sworn report drawn up by Professor Montagnier and filed in a legal action by two lawyers British.

«The CDC and NIAID entered into trade among States (including, but not limited to working with University of North Carolina, Chapel Hill) and with foreign nations (specifically, the Wuhan Institute of Virology and the Chinese Academy of Sciences represented by Zheng-Li Shi) through U19AI109761 (Ralph S. Baric), U19AI107810 (Ralph S. Baric), and National Natural Science Foundation of China Award 81290341 (Zheng-Li Shi) et al. 2015-2016» reads in The Fauci / COVID-19 Dossier.

INTRIGUE WITH THE CIA AND US INTELLIGENCE

«By October 2013, the Wuhan Institute of Virology 1 coronavirus S1 spike protein was described in NIAID’s funded work in China. This work involved NIAID, USAID, and Peter Daszak, the head of EcoHealth Alliance. This work, funded under R01AI079231, was pivotal in isolating and manipulating viral fragments selected from sites across China which contained high risk for severe human response» remembered Martin.

Haines, subsequently, not only in 2018 prophesied a coronavirus epidemic that could only be faced with a new “World Order” but will be one of the main protagonists of the Event 201 exercise held in mid-October in New York thanks to funding from the World Economic Forum by Klaus Schwab (Great Reset) and the Bill & Melinda Gates Foundation.

On the recommendation of the American President Joseph Biden (her longtime political friend) on 21 January 2021 she was appointed by the Senate National Director of Intelligence from where she coordinates all 17 military and civil intelligence agencies and from where she searched, without success. for a rift between 007, to refute the thesis of the artificial origin of SARS-Cov-2.

MODERN STUDIES IN THE SAME YEARS

«By March 2015, both the virulence of the S1 spike protein and the ACE II receptor was known to present a considerable risk to human health. NIAID, EcoHealth Alliance and numerous researchers lamented the fact that the public was not sufficiently concerned about coronavirus to adequately fund their desired research» the dossier still reads in reference to the experiments conducted in a “China-US affair” as Montagnier claimed on the origin of laboratory SARS-Cov-2.

«In 2013, the Autonomous Diagnostics to Enable Prevention and Therapeutics (ADEPT) program awarded grant funding to Moderna Therapeutics for the development of a new type of vaccine based on messenger RNA. The initial DARPA grant was W911NF-13-1-0417» reveals Dr. Martin.

«ON 2015 Moderna signs an agreement for the development of vaccines with NIAID and executes it with the head of the developer and main inventor mRNA-1273 Giuseppe Ciaramella» says Dr. Martin referring to the “prototype” of the experimental antiCovid gene serum named in 2020 Spikevax.

«ON 2016 NIH through Scripps Institute and Dartmouth College file patent application WO 2018081318A1 “Prefusion Coronavirus Spike Proteins and their Use” disclosing mRNA technology that overlaps (and is used in tandem with) Moderna’s technology. Lead Inventor Barney Scott Graham was well known to Moderna as he’s the person at NIH that Moderna “e-mailed” to get the sequence for SARS CoV-2 according to Moderna’s report. In addition, co-inventor Jason McLellan worked with Graham on a vaccine patent jointly owned with the Chinese government filed in Australia in 2013»,

mRNA-1273 – the experimental vaccine developed by Moderna for COVID-19 – uses the LNP technology that Moderna thought it had licensed from Acuitas Therapeutics Inc., a firm developed by a former principal of Arbutus’ prior company Tekmira. That license did not authorize Moderna to use the technology for the COVID-19 vaccine.

«M · CAM and Knowledge Ecology International (Martin’s reference bodies – ed) have independently confirmed that Moderna has violated U.S. law in failing to disclose the U.S. government’s funding interest in their patents and patent applications» reads in The Fauci / Covid-19 Dossier.

«While this negligence impacts all of Moderna’s over 130 granted U.S. patents, it is particularly problematic for U.S. Patent 10,702,600 (‘600) which is the patent relating to, “a messenger ribonucleic acid (mRNA) comprising an open reading frame encoding a betacoronavirus (BetaCoV) S protein or S protein subunit formulated in a lipid nanoparticle».

We have dedicated a long investigation to the mysterious and dangerous biotechnologies with lipid nanoparticles with extensive scientific documentation in relation to the Comirnaty messenger RNA gene serum (“heterozygous twin” of Spikevax), produced by the New Yorker Pfizer with the German Biontech: the first partner of the London-based GSK run by a Microsoft director, the second funded by the same IT tycoon Gates.

THE VACCINE PATENTED 9 MONTHS BEFORE THE PANDEMIC

In addition to the patents cited by the USPTO in their examination of ‘600, M·CAM has identified fourteen other issued patents preceding the ‘600 patent which were used by patent examiners to limit patents arising from the same funded research including patents sought by CureVac.

«In short, while Moderna enjoys hundreds of millions of dollars of funding allegiance and advocacy from Anthony Fauci and his NIAID, since its inception, it has been engaged in illegal patent activity and demonstrated contempt for U.S. Patent law. To make matters worse, the U.S. Government has given it financial backing in the face of undisclosed infringement risks potentially contributing to the very infringement for which they are indemnified» concludes the medical author of The Fauci / Covid-19 Dossier.

But now comes the explosive statement: «The specific claims addressing the pivot to the SARS Coronavirus were patented on March 28, 2019 – 9 months before the SARS CoV-2 outbreak! Both the patent and the DARPA funding for the technology were disclosed in scientific publication (New England Journal of Medicine) but the government funds were not acknowledged in the patent» is Dr. Martin’s shocking revelation.

The patent is updated on 7 July 2020 but was registered for the first time on 28 February 2020 but in continuation of the previous registration of 28 March 2019: the only one not to have changed the patent number (Pat. No.) as is see in the historical extract of the vaccine.

“Continuation of aplication No. 16 / 368,270, filed on Mar.28,2019, which is a continuation of aplication No. 16 / 040,981, filed on Jul.20,2018, now Pat.No. 10,272,150, which is a continuation of aplication No. 15 / 674,599, filed on Aug.1,2017, now Pat.No.10,064,934, which is a continuation of aplication No.PCT / US2016 / 058327, filed on Oct.21,2016 “.

THE EXCHANGE OF DOCUMENTS ON DECEMBER 2019

Analogues suspected on the existence of an experimental gene serum from Moderna before the official discovery of the Wuhan-Hu-1 virus, later identified as a new coronavirus initially named 2019-nCoV because the first cases were recorded in the populated city of Hubei precisely in that year, which was isolated and sequenced as Wuhan MN908947.1 on January 5, 2020.

The first to report the macroscopic anomaly was the British online investigative newspaper The Daily Exposé: «The first to report the macroscopic anomaly was the British online investigative newspaper The Daily Exposé. “A confidentiality agreement shows that potential coronavirus vaccine candidates were transferred from Moderna to the University of North Carolina in 2019, nineteen days before the emergence of the alleged virus causing Covid-19 in Wuhan, China» wrote the British media on June 18, 2021.

«The confidentially agreement (like at the bottom of the page) states that providers ‘Moderna’ alongside the ‘National Institute of Allergy and Infectious Diseases’ (NIAID) agreed to tranfer ‘mRNA coronavirus vaccine candidates’ developed and jointly-owned by NIAID and Moderna to recipients ‘The Universisty of North Carolina at Chapel Hill’ on the 12th December 2019» wrote the editorial staff of Exposé publishing the extracts on pages 105 and 108.

«The material transfer agreement was signed the December 12th 2019 by Ralph Baric, PhD, at the University of North Carolina at Chapel Hill (the microbiologist of the laboratory chimeric SARS virus experiments – ed), and then signed by Jacqueline Quay, Director of Licensing and Innovation Support at the University of North Carolina on December 16th 2019» adds the online newspaper, then asking inevitable questions…

This is taken from a long document. Read the rest here: veteranstoday.com

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