In the ongoing series about the Ukraine War, Mr. Emory has put forth a metaphor: the war itself and the attendant coverage as a “philosopher’s stone” alchemically changing American and Western institutions and individuals into the same political and intellectual fabric of the Ukrainian Institute of National Memory.
That institution is an epicenter of Orwellian historical revisionism, rewriting the World War II history of Ukraine in such a way as to whitewash the war crimes of the OUN and UPA. Bandera headed up the OUN/B, the principal Third Reich collaborator during World War II.
Speaker of the House Nancy Pelosi exemplifies that grim political alchemy.
Prior to a video appearance by Ukrainian President Volodomyr Zelensky, she greeted Zelensky with the OUN/B salute–which is now the official salute of both the Ukrainian military and police establishments.
” . . . . House Speaker Nancy Pelosi on Wednesday, greet Mr. Zelensky with ‘Slava Ukraini!,’—‘Glory to Ukraine’—a greeting used by Bandera’s troops. . . .”
Since the Maidan coup in 2014, we have rigorously chronicled the decisive involvement in that event of the Ukrainian fascist milieu that ascended to the pinnacle of power in that benighted country.
The Nazi collaborationist nature of the regime in power in Ukraine is being systematically whitewashed.
Reflecting on the sheer volume of documentation we have presented about the ascent of the OUN/B Nazis collaborators, we present a couple of snapshots from those archives.
First, we note that Andriy Parubiy–founder of the Social National Party of Ukraine (later re-named Svcoboda)–was one of the organizers of the so-called “Orange Revolution” that brought to power Viktor Yuschenko (and his wife, U.C.C.A. operative and Deputy Director of Public Liaison under R0nald Reagan).
His role as “Commander of Maidan” placed him in close contact with then U.S. Ambassador to Ukraine Geoffrey Pyatt. Then Vice-President Joe Biden was networked with Pyatt at the time. Parubiy has been accused of helping to arrange the sniper fire that killed both protesters and police, leading to the ouster of Yanukovych.
” . . . . Parubiy was going in and out of Hotel Ukraina, from where numerous deadly shots were being fired. . . . Parubiy, who, according to former US Vice President Joe Biden, was conferring with the US Ambassador to Ukraine, Geoffrey Pyatt throughout the upheavals almost on an hourly basis, has never really had his role in the putsch explained. . . .”
Yuschenko elevated Volodymyr Viatrovych to power, eventually becoming head of the Ukrainian Institute of National Memory.
On the subject of propaganda and information war in Ukraine, we note that Zelensky is the point man of that information war and that he is a protege of key Azov financier Igor Kolomoisky.
“Azov” Zelensky is the point element in a—thus far—eminently successful information war. The dimension and success of the propaganda crafted and disseminated OUN/B successor elements in charge of Ukraine’s governmental machinery would make Goebbels proud.
Consummately ironic is the meme resoundingly echoed in this country that PUTIN is waging an information war of lies!
The derisive dismissal of Russian claims concerning animal vectors positioned in Ukraine to deliver biological weapons into Russia ignore critical information.
In addition to the fact that we have developed exhaustive documentation of U.S. authorship of the Covid-19, indicative of a U.S. willingness to employ biological warfare in pursuit of its strategic objectives, Nick Turse chronicled the development of mammalian, reptilian, aquatic and insect life forms as adjuncts to warfare.
This book was published in 2008!
As discussed in FTR#1235, documents removed by the U.S. Embassy in Ukraine–but archived by the Wayback Machine–confirm that the DTRA is among the sources of funding for DOD-financed labs in Ukraine.
We note that there are significant connections between the agency overseeing the Ukrainian projects and institutions implicated in the apparent “bio-skullduggery” surrounding the U.S. biological warfare gambit involving what Mr. Emory has termed “The Oswald Institute of Virology.” This is discussed in: FTR#‘s 1157–1159, 1170, 1183 through 1193, and 1215.
The essence of the “Oswald Institute of Virology” gambit concerns the DTRA and Pentagon funding of bat-borne coronavirus research at the Wuhan Institute of Virology, much of it through Peter Daszak’s EcoHealth Alliance. Once the research was complete, it resulted in publication which included the genome of the bat viruses being researched. Using technology discussed below, the viruses were then synthesized from scratch and population groups were vectored with the same viral strains being researched by the WIV.
One must ask the question, also, as to why the Embassy suddenly removed these documents?
A critical understanding of the virulent, overwhelming lying in which the Ukrainian government is engaging can be gleaned from Mariupol. That city is in control of the Nazi Azov regiment, who control the flow of information from the besieged metropolis.
With Zelensky—a protégé of major Azov financier Igor Kolomoisky—parroting the Nazi formation’s rhetoric and being uncritically accepted by Ukraine’s, it can be said that the West, Biden’s USA in particular, belongs to the lie.
The pronouncements coming out of Mariupol should be understood in the circumstantial context of the fact that all of the international reporters are out of the city.
In addition, the fact that reportage reaching the West has been buttressed by hand-picked advocates of the Zelensky regime should be factored into analysis of the credibility of the battlefield reportage reaching the U.S.
An excellent piece of reporting by Max Blumenthal for the Gray Zone. Noting “Azov” Zelensky’s hyperbole about the “Russian bombing” of the drama theater in Mariupol—Blumenthal reports on local residents’ voluminous accounts of an Azov provocation. Far from being “indiscriminately” bombed by the Russians, Azov appears to have planted and detonated explosive charges, destroying the theater.
Note that the Ukrainian charge of Russia attacking a Turkish mosque was Azov/Zelensky propaganda as well.
Perhaps the most disturbing aspect of this disinformation is the apparent attempt by “Team Azov” to draw the U.S. and NATO into direct conflict with Russia by creating imaginary atrocities, which—thus far—have been uncritically accepted by the West.
Since the Maidan coup in 2014, we have rigorously chronicled the decisive involvement in that event of the Ukrainian fascist milieu that ascended to the pinnacle of power in that benighted country. Ukrainian fascist Andriy Parubiy was the security director of the Maidan demonstrations, an interesting strategic position: ” . . . . Parubiy was going in and out of Hotel Ukraina, from where numerous deadly shots were being fired. . . . Parubiy, who, according to former US Vice President Joe Biden, was conferring with the US Ambassador to Ukraine, Geoffrey Pyatt throughout the upheavals almost on an hourly basis, has never really had his role in the putsch explained. . . .” Ukrainian Presidents Yuschenko and Poroshenko commemorated the OUN at Babi Yar, site of a notorious massacre perpetrated, in part, by OUN/UPA police units. The announcer quotes Adolf Eichmann verbatim in this video from UKRAINE 24. WFMU-FM is podcasting For The Record–You can subscribe to the podcast HERE. Mr. Emory emphatically recommends that listeners/readers get the 32GB flash drive containing all of Mr. Emory’s 43 years on the air, plus a library of old anti-fascist books on easy-to-download PDF files.
This program supplements our long series on “The Oswald Institute of Virology.”
A pair of stories in The Wall Street Journal yield understanding of our media landscape and the degree of propagandizing of same.
Reportage about the WHO’s resumption of its inquiry into the origins of the Covid-19 pandemic hasn’t received much coverage in the U.S.
What coverage there has been has–predictably–focused on the “lack of transparency/cooperation” by China in the probe.
(We reiterate that–at this point in time and sometime before–the Chinese response would have be governed by the disciplines warranted by a wartime investigation of an enemy attack. In this case, a U.S. biological warfare attack. Something of a “bio-Northwoods” operation.)
A remarkable aspect of the Journal’s coverage concerns a development that has been almost completely excised from the Western press: ” . . . . For months, China’s government has insisted both in public, and in private meetings with Dr. Tedros, that studies on the origins of the virus should now focus on other countries, such as Italy, or on a U.S. military bioresearch facility in Fort Detrick, Md. Dozens of governments aligned with China have sent Dr. Tedros letters in support of Beijing’s position, a person familiar with the letters said. . . .”
“Dozens of governments?” Which ones? This sounds like a major international dialogue/scandal.
WHY aren’t we hearing about it?
I think it affords us some perspective on just how carefully manicured the public perspective is in this country.
In another article in the same issue of the Journal, it was noted that Jeffrey Sachs is disbanding the scientific panel he oversaw on behalf of the prestigious British medical journal The Lancet, due to the presence of EcoHealth Alliance chief Peter Daszak and several other members of the panel associated with the organization.
” . . . . Columbia University professor Jeffrey Sachs said he has disbanded a task force of scientists probing the origins of Covid-19 in favor of wider bio-safety research. Dr. Sachs, chairman of a Covid-19 commission affiliated with The Lancet scientific journals, said he closed the task force because he was concerned about its links to EcoHealth Alliance. . . . EcoHealth Alliance’s president, Peter Daszak, led the task force until recusing himself from that role in June. Some other members of the task force have collaborated with Dr. Daszak or EcoHealth Alliance on projects. . . . .”
EcoHealth Alliance has been heavily involved in coronavirus research–including gain-of-function work–at the Wuhan Institute of Virology. We have noted that the DARPA has been heavily involved with that category of research.
As noted in past programs and discussion, the EcoHealth Alliance is funded primarily by the Department of Defense and USAID, a State Department subsidiary that has often served as a cover for CIA operations. One of the principal advisers of the organization is David Franz, the former commanding officer of Fort Detrick.
Worth noting is that Jeffrey Sachs–an American economics professor–was tabbed to select those personnel to serve on a panel of experts assembled under the auspices of The Lancet–a British medical journal.
In addition to his role advising both Bernie Sanders and Alexandria Ocasio-Cortez, Sachs headed the U.S. government-funded Harvard University consortium that advised Boris Yeltsin and, in the process, drove Russia back to the stone age.
In Russia, it is widely believed that Sachs work for the CIA–a theory that is bolstered by his pivotal role in managing the narrative concerning the origins of the pandemic.
We have done many programs underscoring our working hypothesis that Covid-19 is a biological warfare weapon, developed by the U.S. and deployed as part of the destabilization program against China we have covered since the fall of 2019.
(Some of those programs are: FTR#‘s 1157, 1158, 1159, 1170 and FTR#‘s 1183 through 1193, inclusive.)
Next, we highlight a heavily “spun” story about the EcoHealth Alliance and its involvement with Pentagon-linked research into bat-borne coronaviruses may well–when freed from the predictably ideologized journalistic shading to which it has been subjected–yield a “smoking genome” with regard to the SARS CoV‑2 virus causing the Covid-19 pandemic.
(The Intercept is the spawn of Pierre Omidyar, deeply involved in the ascent of the Nazi OUN/B milieu in Ukraine and that of the Hindutva fascist regime of Narendra Modi in India. He has partnered with U.S. intelligence cutouts such as the National Endowment for Democracy and USAID. Omidyar’s protege Glenn Greenwald is to be viewed with a jaundiced eye as well.)
Key points of information in the article:
1.–” . . . . Last month, a grant application submitted to the US Defense Advanced Research Projects Agency (Darpa) revealed that an international team of scientists had planned to mix genetic data of similar strains to create a new virus. The grant application was made in 2018 . . . .”
2.–” . . . . The grant application proposal was submitted by British zoologist Peter Daszak on behalf of a group, which included Daszak EcoHealth Alliance, the Wuhan Institute of Virology, the University of North Carolina and Duke NUS in Singapore, The Telegraph reported. . . .”
3.–” . . . . ‘We will compile sequence/RNAseq data from a panel of closely related strains and compare full length genomes, scanning for unique SNPs representing sequencing errors. ‘Consensus candidate genomes will be synthesised commercially using established techniques and genome-length RNA and electroporation to recover recombinant viruses,’ the application states. . . .”
4.–” . . . . The WHO expert told The Telegraph that the process detailed in the application would create ‘a new virus sequence, not a 100 per cent match to anything.’ ‘They would then synthesise the viral genome from the computer sequence, thus creating a virus genome that did not exist in nature but looks natural as it is the average of natural viruses. ‘Then they put that RNA in a cell and recover the virus from it. ‘This creates a virus that has never existed in nature, with a new ‘backbone’ that didn’t exist in nature but is very, very similar as it’s the average of natural backbones,’ the expert said. . . .”
5.–” . . . . Experts told the paper that creating an ‘ideal’ average virus could have been part of work to create a vaccine that works across coronaviruses. Last month, it emerged that the US had funded similar research to that outlined in the 2018 grant proposal. . . .”
Key considerations in the context of which this story should be viewed:
1.–DARPA has been extensively involved in researching bat-borne coronaviruses in, and around China.
2.–Note that the proposal to DARPA involved extensive discussion of the genome of the virus to be synthesized. Utilizing contemporary technology, this would permit the synthesis of the virus without necessarily approving the proposal!
3.–Note that the latest innovations in biotechnology permit: ” . . . . Advances in the area mean that scientists now have the capability to recreate dangerous viruses from scratch; make harmful bacteria more deadly; and modify common microbes so that they churn out lethal toxins once they enter the body. . . .”
4.–Those innovations also permit: ” . . . . In the report, the scientists describe how synthetic biology, which gives researchers precision tools to manipulate living organisms, ‘enhances and expands’ opportunities to create bioweapons. . . .”
5.–Those innovations also permit: ” . . . . Today, the genetic code of almost any mammalian virus can be found online and synthesized. ‘The technology to do this is available now,’ said [Michael] Imperiale. ‘It requires some expertise, but it’s something that’s relatively easy to do, and that is why it tops the list.’ . . .”
6.–The chief funding sources for the EcoHealth Alliance are the Pentagon and USAID, a State Department subsidiary that commonly serves as a cover for CIA.
7.–One of Peter Daszak’s chief advisers is David Franz, the former commanding officer of Fort Detrick.
8.–In FTR#1191, we noted that producing a vaccine for an existing biological weapon or one under advanced development might well be seen as an “offensive” biological warfare maneuver.
9.–This article, like many others, features commentary from Richard Ebright to the effect that the WIV did, in fact, synthesize the virus. Ebright had a long association with the Howard Hughes Medical Institute, the former owner of the Hughes Aircraft Company, a firm with profound national security connections. It is more than a little interesting that Ebright, like almost all of the other commenters quoted in the U.S., does not factor in the innovations in biotechnology highlighted above.
10.–Of interest, as well, is this passage: ” . . . . Experts told the paper that creating an ‘ideal’ average virus could have been part of work to create a vaccine that works across coronaviruses. Last month, it emerged that the US had funded similar research to that outlined in the 2018 grant proposal. . . .”
11.–The Pentagon has, indeed, been working on such a vaccine: ” . . . . The service is closing in on a ‘pan-coronavirus’ vaccine and on synthetic antibodies that could protect a population before spread. . . .”
Pompeo State Department officials pursuing the lab-leak hypothesis were told to cover it up lest it shed light on U.S. government funding of research at the “Oswald Institute of Virology!”: ” . . . . In one State Department meeting, officials seeking to demand transparency from the Chinese government say they were explicitly told by colleagues not to explore the Wuhan Institute of Virology’s gain-of-function research, because it would bring unwelcome attention to U.S. government funding of it. . . . In an internal memo obtained by Vanity Fair, Thomas DiNanno, former acting assistant secretary of the State Department’s Bureau of Arms Control, Verification, and Compliance, wrote that. . . staff from two bureaus . . . ‘warned’ leaders within his bureau ‘not to pursue an investigation into the origin of COVID-19’ because it would ‘open a can of worms’ if it continued.’ . . . . As the group probed the lab-leak scenario, among other possibilities, its members were repeatedly advised not to open a ‘Pandora’s box,’ said four former State Department officials interviewed by Vanity Fair. . . .”
New York Times right-wing columnist Ross Douthat has highlighted the propaganda significance of pinning the “Lab Leak Theory” on China.
In an ironic tragedy worthy of Aeschylus, Douthat has been struggling with Lyme Disease, and has suffered greatly in his attempts to navigate the Lyme Disease treatment labyrinth. We have done many programs on Lyme Disease and its development as a biological warfare weapon.
Interviewed by an indie filmmaker named Tim Grey, Willy Burgdorfer discussed the development of Lyme Disease as a biological warfare weapon. It was Burgdorfer who “discovered” the spirochete that caused Lyme Disease in 1982. As we will see later, it appears that more than one organism is involved with Lyme Disease.
1.–” . . . . Willy paused, then replied, ‘Question: Has [sic] Borrelia Burgdorferi have the potential for biological warfare?’ As tears welled up in Willy’s eyes, he continued, ‘Looking at the data, it already has. If the organism stays within the system, you won’t even recognize what it is. In your lifespan, it can explode . . . We evaluated. You never deal with that [as a scientist]. You can sleep better.’ . . .”
2.–” . . . . Later in the video, Grey circled back to this topic and asked, ‘If there’s an emergence of a brand-new epidemic that has the tenets of all of those things that you put together, do you feel responsible for that?’ ‘Yeah. . . .’ ”
3.–” . . . . Grey asked him the one question, the only question, he really cared about: ‘Was the pathogen that you found in the tick that Allen Steere [the Lyme outbreak investigator] gave you the same pathogen or similar, or a generational mutation, of the one you published in the paper . . . the paper from 1952?’ ”
4.–” . . . . The left side of his mouth briefly curled up, as if he is thinking, ‘Oh, well.’ Then anger flashes across his face. ‘Yah,’ he said, more in German than English. . . .”
5.–” . . . . It was a stunning admission from one of the world’s foremost authorities on Lyme disease. If it was true, it meant that Willy had left out essential data from his scientific articles on the Lyme disease outbreak, and that as the disease spread like a wildfire in the Northeast and Great Lakes regions of the United States, he was part of the cover-up of the truth. . . It had been created in a military bioweapons lab for the specific purpose of harming human beings. . . . ”
Next, we present discussion of Ms. Newby’s expose of the institutionally and financially incestuous relationship between bureaucratic and corporate entities that both regulate, and profit from, Lyme Disease. Key “experts” involved with diagnosing and treating the affliction run interference for the status quo.
Legal and regulatory rulings have enabled the patenting of living organisms and that has exacerbated the monetizing of Lyme Disease treatment. That monetization, in turn, has adversely affected the quality of care for afflicted patients. ” . . . . All of a sudden, the institutions that were supposed to be protectors of public health became business partners with Big Pharma. The university researchers who had previously shared information on dangerous emerging diseases were now delaying publishing their findings so they could become entrepreneurs and profit from patents through their university technology transfer groups. We essentially lost our system of scientific checks and balances. And this, in turn, has undermined patient trust in the institutions that are supposed to ‘do no harm.’ . . .”
Strikingly, a FOIA suit she filed was stonewalled for five years, before finally yielding the documents she had so long sought.
The “experts” and their agenda were neatly, and alarmingly, summed up by Ms. Newby:
” . . . . The emails revealed a disturbing picture of a nonofficial group of government employees and guidelines authors that had been setting the national Lyme disease research agenda without public oversight or transparency. . . . Bottom line, the guidelines authors regularly convened in government-funded, closed-door meetings with hidden agendas that lined the pockets of academic researchers with significant commercial interests in Lyme disease tests and vaccines. A large percentage of government grants were awarded to the guideline authors and/or researchers in their labs. Part of the group’s stated mission, culled from these FOIA emails, was to run a covert ‘disinformation war’ and a ‘sociopolitical offensive’ to discredit Lyme patients, physicians, and journalists who questioned the group’s research and motives. In the FOIA-obtained emails, Lyme patients and their treating physicians were called ‘loonies’ and ‘quacks’ by Lyme guidelines authors and NIH employees. . . .”
We conclude with review of a chilling set of provocations that were planned by the Joint Chiefs of Staff in the early 1960s. Although they were not formally instituted at that time, Mr. Emory believes the scenarios discussed below have been adapted to the modern, high-technology available to biological warfare practitioners and instituted as the Covid-19 “op.”
Move over COVID. 2021 is turning out to be another year of the digital virus. One massive hacking story after another. Unrelated stories in many cases, we are told. In particular:
1. The SolarWinds mega-hack announced in December of 2020, blamed on Russia, blamed on Cozy Bear
2. The Microsoft Exchange mega-hack disclosed in March 2021, blamed on China.
3. The revelations about NSO Group’s oversight (or lack thereof) of its powerful spyware sold to governments around the world.
4. The emerging story of Candiru, one of NSO Group’s fellow “commercial surveillance vendors”, selling toolkits overflowing with zero-day exploits, specializing in targeting Microsoft products.
But how unrelated are these stories? That’s the big question we’re going to explore in this post. A question punctuated by another meta-story we’ve looked at many times before: the meta-story of a cyberattribution paradigm seemingly designed to allow private companies and governments to concoct an attribution scenario for whatever guilty party they want to finger. As long as there was some sort of ‘clue’ found by investigators — like piece of Cyrillic or Mandarin text or malware previously attributed to a group — these clues were strung together in a “pattern recognition” manner to arrive at a conclusion about the identity of the perpetrators. Attribution conclusions often arrived at with incredible levels of confidence. Recall how the Japanese cybersecurity firm TrendMicro attributed a 2017 US Senate email phishing campaign to ‘Pawn Storm’/Fancy Bear with 100 percent certainty, and they made this highly certain attribution based heavily on how similar the hack was to the 2017 hacks of Emmanuel Macron’s emails via a phishing campaign that TrendMicro attributed at the time with 99 percent certainty to Pawn Storm/Fancy Bear and yet the ANSSI, the French government’s cybersecurity agency, was leaving open the possibility that the hack they could be the work of “other high-level” hackers trying to pin the blame on “Pawn Storm” (another name for “Fancy Bear”). TrendMicro was making 99 percent certain attributions that the French government said could be any range of actors. That was the state of affairs for cyberattributions in 2017 and nothing has changed in the years since. Highly certain attributions continued to be piled on top of highly certain attributions — almost always pointing towards Russian, Iran, China, or North Korea — built on a foundation of what appear to be largely guesswork. Often highly motivated guesswork (i.e. lies).
This post supplements and is intended to call attention to FTR #‘s 1157, 1158 and 1159. A consummately important article about Peter Daszak (right) and the EcoHealth Alliance provides troubling insights into the uneven professional track record of Daszak and the profound involvement of the organization he heads with the Pentagon and other U.S. national security establishment institutions. Exemplifying EcoHealth Alliance’s work is a Pentagon contract with Tanzania, researching CCHF–Crimean-Congo Hemorrhagic Fever. ” . . . . EcoHealth Alliance has a $5‑million Pentagon contract, ‘Crimean-Congo Hemorrhagic Fever: Reducing an Emerging Health Threat in Tanzania.’ Crimean-Congo Hemorrhagic Fever (CCHF) is a tick-borne disease, originally only infecting animals. . . . There was only ever one case of CCHF in Tanzania, and that was in 1986. . . . Gain-of-function research on CCHF is being conducted at the U.S. Department of Agriculture’s National Bio and Agro-Defense Facility (NBAF) . . . . (The National Bio and Agro Defense Facility will take over the mission of the Plum Island Animal Disease Center and become the lead facility for Foreign Animal Disease research.) . . .”
A noteworthy development in the Covid-19 “op” concerns the selection of experts to oversee The Lancet’s investigation of the origins of the SARS CoV‑2.
In FTR #1156, we looked at the involvement of known U.S. intelligence cut-outs–notably USAID–and their funding of programs ostensibly aimed at preventing epidemics. Those programs involved the “Gain-of-Function” mutation of bat-borne coronaviruses, creating novel “chimeric” viruses that never existed before.
The ostensible purpose was to “prevent” future epidemics. We wondered in FTR #1156 if those ostensible epidemic “prevention” programs may have masked epidemic propagation programs, rather like Unit 731.
Peter Daszak of the EcoHealth Alliance was selected to lead the project.
His perspective would, on the surface, appear to be less than objective, in as much as he championed the very type of GOF experiments that are at the center of this inquiry.
Of interest, as well, is the selection of Jeffrey Sachs, an economist, member of the [Bernie] Sanders Institute, economic adviser to Bernie Sanders, economic adviser to AOC and, most importantly, head of the [partly] government financed Harvard Institute of International Development which (as advisers to Boris Yeltsin) drove the Russian economy back to the Stone Age.
Sachs has no medical or scientific credentials.
A consummately important article about Daszak and the EcoHealth Alliance provides troubling insights into the uneven professional track record of Daszak and the profound involvement of the organization he heads with the Pentagon and other U.S. national security establishment institutions.
EcoHealth Alliance looks disturbingly like an organization that fronts for elements and individuals involved with biological warfare research.
“Peter Daszak, President of EcoHealth Alliance, is a top scientific collaborator, grantwriter and spokesperson for virus hunters and gain-of-function/dual-use researchers, in labs both military and civilian.
Daszak works with dozens of high-containment laboratories around the world that collect pathogens and use genetic engineering and synthetic biology to make them more infectious, contagious, lethal or drug-resistant. These include labs controlled by the U.S. Department of Defense, in countries in the former Soviet Union, the Middle East, South East Asia and Africa.
Many of these labs are staffed by former biological weapons scientists. (See Arms Watch’s reports.) Before the Biological Weapons Convention was ratified, this research was called what it is: biological weapons research. Now, it’s euphemistically called gain-of-function or dual-use research.
Gain-of-function research to alter coronaviruses for the infection of humans goes back to 1999 or earlier, years before the first novel coronavirus outbreak. On behalf of the U.S. government, often the military, Daszak scours the globe for animal pathogens and brings them back to the lab to be catalogued, investigated and manipulated. . . .”
Key points of analysis and discussion include:
1.–EcoHealth Alliance contracts with the Pentagon in Tanzania, South Africa, Georgia and Malaysia, as well as the U.S.
2.–” . . . . A recent Wired magazine article quoting Daszak described how a virus collected in 2012 was found to be a 96-percent match to SARS-CoV‑2 in 2020 . . . ‘a lack of funding meant they couldn’t further investigate the virus strain now known to be 96 percent genetically similar to the virus that causes Covid-19’ . . . .”
3.–Daszak’s claim that they couldn’t further investigate that virus because of a lack of funding is dubious, in that recent grants to the organization are on top of ” . . . . $100.9 million that EcoHealth Alliance has received in government grants and contracts since 2003. . . .”
4.–Daszak does not explain how that virus (discovered in 2012) turned into SARS-CoV‑2. ” . . . . Some scientists say it would take 50 years for RaTG13 [the virus in question–D.E.] to turn into SARS-CoV‑2. . . .”
5.–Daszak is heavily networked with the Department of Homeland Security: ” . . . . the Department of Homeland Security’s National Biosurveillance Integration Center (NBIC) . . . . gave Daszak’s EcoHealth Alliance a $2.2‑million contract (2016–2019) to create a ‘Ground Truth Network’ of ‘subject matter experts’ who could provide ‘contextual information pertaining to biological events.’ . . . .”
6.–The intellectual and professional track record of Daszak and EcoHealth Alliance is porous. EcoHealth Alliance floated a canard about Ebola potentially traveling to the U.S. ” . . . . an EcoHealth Alliance spokesperson, spread a false (not to mention racist and xenophobic) narrative, one that subsequently would be thoroughly debunked, that bushmeat smuggled to the U.S. from Africa could transmit Ebola to Americans. . . .”
7.–Daszak missed the boat badly with regard to SARS: ” . . . . It is commonly accepted that the SARS pandemic began in 2002, when humans caught a bat virus from civet cats at a wet market in Guangdong, China. But Daszak and his collaborators admit they have no evidence to explain how the virus leapt from bats to civets to humans. . . .”
8.–” . . . . SARS-CoV was found in civets at the Guangdong wet market, but civets aren’t the natural reservoir of this virus. Bats are. Only the civets at the market—and no farm-raised or wild civets—carried the virus. None of the animal traders handling the civets at the market had SARS. . . .”
9.–” . . . . When Daszak and his collaborators at the WIV searched the cave in Yunnan for strains of coronavirus similar to human versions, no single bat actually had SARS. Genetic pieces of the various strains would have to be recombined to make up the human version. Adding to the confusion, Yunnan is about 1,000 kilometers from Guangdong. . . .”
10.–” . . . . So, how did viruses from bats in Yunnan combine to become deadly to humans, and then travel to civets and people in Guangdong, without causing any illnesses along the way during this 1,000 kilometer trip? . . .”
11.–Daszak and the EcoHealth Alliance were deeply involved with a USAID and NIH funded joint WIV/University of North Carolina project we have covered extensively in past programs. ” . . . . The two institutions also worked as collaborators under another $2.6‑million grant, ‘Risk of Viral Emergence from Bats,’ and under EcoHealth Alliance’s largest single source of funding, a $44.2 million sub-grant from the University of California at Davis for the PREDICT project (2015–2020). . . .”
12.–” . . . . It’s the $44.2‑million PREDICT grant that EcoHealth Alliance used to fund the gain-of-function experiment by WIV scientist Zhengli Shi and the University of North Carolina at Chapel Hill’s Ralph Baric. Shi and Baric used genetic engineering and synthetic biology to create a ‘new bat SARS-like virus . . . that can jump directly from its bat hosts to humans.’ . . .”
13.–” . . . . The work . . . published in Nature in 2015 during the NIH’s moratorium on gain-of-function research, was grandfathered in because it was initiated before the moratorium (officially called the U.S. Government Deliberative Process Research Funding Pause on Selected Gain-of-Function Research Involving Influenza, MERS and SARS Viruses), and because the request by Shi and Baric to continue their research during the moratorium was approved by the NIH. . . .”
14.–” . . . . As a condition of publication, Nature, like most scientific journals, requires authors to submit new DNA and RNA sequences to GenBank, the U.S. National Center for Biotechnology Information Database. Yet the new SARS-like virus Shi and Baric created wasn’t deposited in GenBank until May 2020. . . .”
15.–” . . . . why is the government focusing on just one of EcoHealth Alliance’s projects, when the organization has received $100.9 million in grants, primarily from the Department of Defense, to sample, store and study bat coronaviruses at labs around the world? Coronaviruses, both those that have been collected from animals and those that have been created through genetic engineering and synthetic biology, at all of these labs should be compared with SARS-CoV‑2. . . . .”
16.–” . . . . Daszak’s collaborators working under contracts with the Department of Health and Human Services (HHS) aren’t allowed to conduct gain-of-function research unless specifically approved to do so by the Potential Pandemic Pathogen Care and Oversight (P3CO) committee. This committee was set up as a condition for lifting the 2014–2017 moratorium on gain-of-function research. The P3CO committee operates in secret. Not even a membership list has been released. . . .”
17.–Exemplifying EcoHealth Alliance’s work is a Pentagon contract with Tanzania, researching CCHF–Crimean-Congo Hemorrhagic Fever. ” . . . . EcoHealth Alliance has a $5‑million Pentagon contract, ‘Crimean-Congo Hemorrhagic Fever: Reducing an Emerging Health Threat in Tanzania.’ Crimean-Congo Hemorrhagic Fever (CCHF) is a tick-borne disease, originally only infecting animals. . . . There was only ever one case of CCHF in Tanzania, and that was in 1986. . . . Gain-of-function research on CCHF is being conducted at the U.S. Department of Agriculture’s National Bio and Agro-Defense Facility (NBAF) . . . . (The National Bio and Agro Defense Facility will take over the mission of the Plum Island Animal Disease Center and become the lead facility for Foreign Animal Disease research.) . . .”
Program Highlights Include: The prominent role in the Sanders Institute and AOC’s advisory team of Jeffrey Sachs, whose HIID team of advisers (with government funding) sent Russia back to the Stone Age, economically; the “handoff” to Jeffrey Sachs and his HIID of Russia and other former Soviet Republics by the Gehlen/GOP Nazis manifesting through the Free Congress Foundation; review of the operational political continuum stretching from the Third Reich, through the OSS, the CIA and the GOP; review of the roles of Allen Dulles, William Casey, Resorts International and Donald Trump in that continuum.
As indicated by the title of the program, this broadcast updates various articles and book excerpts concerning Covid-19.
A Daily Mail Online [UK] article sets forth two bogus papers contending that the SARS CoV‑2 virus was genetically engineered by the Chinese as a bioweapon in a laboratory and that it “escaped.” Note the championing of one of the papers by a former head of MI6 and the authorship of the second by The Epoch Times, the paper of the Falun Gong cult. Linked to CIA, Steve Bannon’s anti-China milieu and the Trump administration, the organization is a fascist mind control cult discussed in numerous shows, including FTR #‘s 1089 and 1090.
1.–“A former MI6 chief was yesterday accused by Government officials of peddling ‘fanciful claims’ that coronavirus was accidentally created in a Chinese laboratory. British security agencies believe Covid-19 is not a man-made virus and is ‘highly likely’ to have occurred naturally and spread to humans through animals. And Health Secretary Matt Hancock has said there is ‘no evidence’ to back up the theory that it originated in a laboratory. But Sir Richard Dearlove, who was head of the MI6 from 1999 to 2004, cited a recent report claiming the disease was accidentally manufactured by Chinese scientists.
2.–“ ‘I do think that this started as an accident,’ Sir Richard told The Daily Telegraph’s ‘Planet Normal’ podcast. ‘It raises the issue: if China ever were to admit responsibility, does it pay reparations? I think it will make every country in the world rethink how it treats its relationship with China.’ He added: ‘Look at the stories... of attempts by the [Beijing] leadership to lock down any debate about the origins of the pandemic and the way people have been arrested or silenced.’ . . . . The paper – co-authored by Professor Angus Dalgleish, a renowned oncologist and vaccine researcher who works at St George’s Hospital, University of London, and Birger Sorensen, a Norwegian virologist – contains none of the stark allegations that originally stunned its reviewers.
3..–“The initial paper that triggered wild rumours failed stringent tests of verification and is understood to have been rejected in April by eminent international journals such as Nature and the Journal of Virology. Biomedical experts from the Francis Crick Institute and Imperial College London are said to have refuted its conclusions. Then one of the paper’s co-authors, Dr John Fredrik Moxnes, chief scientific adviser to the Norwegian military, asked for his name to be withdrawn. This week, after numerous rewrites, the paper was published by the Quarterly Review of Biophysics Discovery. And those original world-shaking conclusions have now withered to innuendo. No accusation of Chinese manipulation appears. . . .”
4.–”. . . . Back in April, a slickly produced investigative documentary, Tracking Down The Origin Of The Wuhan Coronavirus, was released online. It claimed conclusive proof that the Covid-19 virus had been created as a biological ‘weapon of mass destruction’ in a Chinese lab. . . .”
5.–“At first sight, it seemed a shockingly convincing piece of journalism. On behalf of this newspaper, I cross-checked every claim: The experts it cited and the factual evidence unearthed. I also researched the backgrounds of its makers. I then approached some of the world’s best independent scientific authorities to ask their opinion. They all agreed – this enticingly spicy story just didn’t stand up.”
6.–“It had been produced by a US based anti-Chinese government media organisation called the Epoch Times. Its ‘experts’ were veteran hard-Rightists. Most damningly, its scientific ‘facts’ were twisted out of shape.So much, then, for the Chinese-manufactured coronavirus conspiracy . . .”
Steve Bannon is at the epicenter of the anti-China effort and–to no one’s surprise–never really left the Trump White House.
When assessing Bannon as a political animal, one should never forget that among the important ideological influences on him is Julius Evola, an Italian fascist who found Mussolini too moderate and ultimately took his cues from the Nazi SS, who were financing his work by the end of World War II.
” . . . . Donald Trump’s lightning-rod 2016 campaign boss and former White House chief strategist who was banished from the West Wing in 2017 has quietly crept back into 1600 Pennsylvania Ave., reestablishing ties to staffers, particularly with regard to his pet issues of China and immigration. . . . Another former administration official told The Post that Bannon never really left the White House after he was fired, maintaining contacts and keeping up regular channels of communications with officials there. . . .”
In addition, as discussed in FTR #‘s 1111 and 1112, Bannon is part of a network that includes J. Kyle Bass and Tommy Hicks, Jr. This nexus involves asymmetrical investing with regard to the Hong Kong and Chinese economies and the inter-agency governmental networks involved in both overt and covert anti-China policies implemented by Team Trump. As will be seen below, they also are networking with the mis-named “Scientists to Stop Covid-19.” In that regard, they are also helping steer policy that controls development of treatment and vaccines for Covid-19. The management of drug and vaccine development, in turn, doubles back to market-driving investment dynamics.
An interesting summation of characteristics of a “deliberate” epidemic are evaluated against the finding that New York City was the epicenter of the U.S. Covid-19 outbreak:
Bitten: The Secret History of Lyme Disease and Biological Weapons by Kris Newby; HarperCollins [HC]; Copyright 2019 by Kris Newby; ISBN 9780062896728; p. 185.
Potential epidemiological clues to a deliberate epidemic:
Clue no. 1–A highly unusual event with large numbers of casualties: Check!
Clue no. 2–Higher morbidity or mortality than is expected. Check!
Clue no. 3–Uncommon disease. Check!
Clue no. 4–Point-source outbreak. Check!
Clue no. 5–Multiple epidemics. Check! (Global pandemic)
–Z. F. Dembek, et al., “Discernment Between Deliberate and Natural Infectious Disease Outbreaks”
The prevailing view of the Covid-19 outbreak contends that the American outbreak spread outward from New York City. The strain of SARS CoV‑2 that appeared in New York came, in turn, from Europe.
This doesn’t make sense. There were confirmed cases of the virus on the West Coast that did not come from New York. A European strain of the virus transmitted to New York City would have come in via air. In such an event, there would have been a well-documented outbreak of Covid-19 among flight attendants, who operate in close contact with passengers in cramped circumstances, as well as experiencing jet lag, which compromises the immune system.
Next, we review an aspect of the 2001 anthrax attacks. We highlighted the 2001 anthrax attacks in connection with the Covid-19 outbreak in New York City in FTR #1128.
We note that the Anthrax attacks appear to have operated in overlapping contexts, including justification for the war in Iraq.
The 2001 anthrax attacks appear to have served as a provocation that justified a ten-fold increase in spending for biological warfare development. The number of BSL‑4 labs (having dual civilian and military use) increased from two in 2001, to a dozen in 2007.
This increase occurred while Donald Rumsfeld was George W. Bush’s secretary of defense. He went to that position from being Chairman of the Board of Directors for Gilead Sciences, the manufacturer of remdesivir.
We will delve into the politics of the anthrax attacks in the future.
In the context of the above article, note that the National Institutes of Health have also partnered with CIA and the Pentagon, as underscored by an article about a BSL‑4 lab at Boston University. Note that Europe and the U.S. have twelve BSL4 labs apiece. Taiwan has two. China has one:
1.–As the article notes, as of 2007, the U.S. had “more than a dozen” BSL4 labs–China commissioned its first as of 2017. a tenfold increase in funding for BSL4 labs occurred because of the anthrax attacks of 2001. Those attacks might be seen as something of a provocation, spurring a dramatic increase in “dual use” biowarfare research, under the cover of “legitimate” medical/scientific research. In FTR #1128, we hypothesized about the milieu of Stephen Hatfill and apartheid-linked interests as possible authors of a vectoring of New York City with Sars COV2: ” . . . . Before the anthrax mailings of 2001, the United States had just two BSL4 labs—both within the razor-wire confines of government-owned campuses. Now, thanks to a tenfold increase in funding—from $200 million in 2001 to $2 billion in 2006—more than a dozen such facilities can be found at universities and private companies across the country. . . .”
2.–The Boston University lab exemplifies the Pentagon and CIA presence in BSL‑4 facility “dual use”: ” . . . . But some scientists say that argument obscures the true purpose of the current biodefense boom: to study potential biological weapons. ‘The university portrays it as an emerging infectious disease lab,’ says David Ozonoff, a Boston University epidemiologist whose office is right across the street from the new BSL4 facility. ‘But they are talking about studying things like small pox and inhalation anthrax, which pose no public health threat other than as bioweapons.’ . . . The original NIH mandate for the lab indicated that many groups—including the CIA and Department of Defense—would be allowed to use the lab for their own research, the nature of which BU might have little control over. . . .”
Pivoting to discussion and review of the political, financial and corporate connections to the development of medicinal treatments for, and vaccines to prevent, Covid-19, we recap details relevant to the extraordinary timing of a 4/29 announcement of favorable results for a trial of remdesivir. That announcement drove equities markets higher and was beneficial to the stock of Gilead Sciences.
We present a Stat News article on the internal deliberations behind the decisions to modify the NIAID study. Of particular significance is the DSMB deliberation. Note the timeline of the DSMB deliberation, combined with the announcement on 4/29 that drove the markets higher.
1.–The decision was made to cut it short before the question of remdesivir’s impact on mortality could be answered: ” . . . .The National Institute of Allergy and Infectious Diseases has described to STAT in new detail how it made its fateful decision: to start giving remdesivir to patients who had been assigned to receive a placebo in the study, essentially limiting researchers’ ability to collect more data about whether the drug saves lives — something the study, called ACTT‑1, suggests but does not prove. In the trial, 8% of the participants given remdesivir died, compared with 11.6% of the placebo group, a difference that was not statistically significant. A top NIAID official said he had no regrets about the decision. ‘There certainly was unanimity within the institute that this was the right thing to do,’ said H. Clifford Lane, NIAID’s clinical director. . . .”
2.–In addition, patients scheduled to receive placebo received remdesivir, instead. ” . . . . Steven Nissen, a veteran trialist and cardiologist at the Cleveland Clinic, disagreed that giving placebo patients remdesivir was the right call. ‘I believe it is in society’s best interest to determine whether remdesivir can reduce mortality, and with the release of this information doing a placebo-controlled trial to determine if there is a mortality benefit will be very difficult,’ he said. ‘The question is: Was there a route, or is there a route, to determine if the drug can prevent death?’ The decision is ‘a lost opportunity,’ he said. . . .”
3.–Steven Nissen was not alone in his criticism of the NIAID’s decision. ” . . . .Peter Bach, the director of the Center for Health Policy and Outcomes at Memorial Sloan Kettering Cancer Center, agreed with Nissen. ‘The core understanding of clinical research participation and clinical research conduct is we run the trial rigorously to provide the most accurate information about the right treatment,’ he said. And that answer, he argued, should ideally have determined whether remdesivir saves lives. The reason we have shut our whole society down, Bach said, is not to prevent Covid-19 patients from spending a few more days in the hospital. It is to prevent patients from dying. ‘Mortality is the right endpoint,’ he said. . . .”
4.–Not only was the administration of remdesivir instead of placebo prioritized, but the NIAID study itself was attenuated! ” . . . . But the change in the study’s main goal also changed the way the study would be analyzed. Now, the NIAID decided, the analysis would be calculated when 400 patients out of the 1,063 patients the study enrolled had recovered. If remdesivir turned out to be much more effective than expected, ‘interim’ analyses would be conducted at a third and two-thirds that number.The job of reviewing these analyses would fall to a committee of outside experts on what is known as an independent data and safety monitoring board, or DSMB. . . .”
5.–The performance of the DSMB for the remdesivir study is noteworthy: ” . . . . But the DSMB for the remdesivir study did not ever meet for an interim efficacy analysis, Lane said. All patients had been enrolled by April 20. The data for a DSMB meeting was cut off on April 22. The DSMB met and, on April 27, it made a recommendation to the NIAID. . . .”
The DSMB meeting on 4/27 determined the switch from placebo to remdesivir. Of paramount importance is the fact that this was JUST BEFORE the 4/29 announcement that drove the markets higher and the same day on which key Trump aide–and former Gilead Sciences lobbyist Joe Grogan resigned! ” . . . . . That decision, Lane said, led the NIAID to conclude that patients who had been given placebo should be offered remdesivir, something that started happening after April 28. . . .”
6.–Dr. Ethan Weiss gave an accurate evaluation of the NIAID study: ” . . . . ‘We’ve squandered an incredible opportunity to do good science,’ [Dr. Ethan] Weiss said. ‘If we could ever go back and do something all over, it would be the infrastructure to actually learn something. Because we’re not learning enough.’ . . . .”
The remarkable handling of the NIAID study, the timing of the announcement of the altogether limited success of the attenuated trial and the rise in equities as a result of the announcement may be best understood in the context of the role played in Trump pandemic decision-making by an elite group of billionaires and scientists–including convicted felon Michael Milken (the “junk bond king”).
1.–” . . . . Calling themselves ‘Scientists to Stop COVID-19,’ the collection of top researchers, billionaires and industry captains will act as an ‘ad hoc review board’ for the torrent of coronavirus research, ‘weeding out’ flawed data before it reaches policymakers, the Wall Street Journal reported on Monday. They are also acting as a go-between for pharmaceutical companies seeking to build a communication channel with Trump administration officials. The group . . . . has advised Nick Ayers, an aide to Vice President Mike Pence, as well as other agency heads, in the past month. Pence is heading up the White House coronavirus task force. . . .”
2.–” . . . The brainy bunch is led by Thomas Cahill, a 33-year-old doctor who became a venture capitalist . . . . Cahill’s clout comes from building connections through his investment firm, Newpath Partners, with Silicon Valley’s Peter Thiel, the founder of PayPal, and billionaire businessmen Jim Palotta and Michael Milken. . . .”
Note that Peter Thiel played a dominant role in bankrolling Newpath Partners, and the other financial angel who elevated Cahill–Brian Sheth–introduced him to Tommy Hicks, Jr., the co-chairman of the RNC. In FTR #‘s 1111 and 1112, we looked at Hicks’ networking with Steve Bannon associate J. Kyle Bass, as well as his role in the inter-agency networks driving the anti-China effort.
” . . . . At the helm of the effort: The 33-year-old and very-much-under-the-radar venture capitalist Tom Cahill, who leads life sciences-focused Newpath Partners. Cahill completed his M.D. and PhD at Duke University a mere two years ago before landing at blue-chip investment firm Raptor Group through a friend. He went on to found Newpath with some $125 million after impressing well-connected names like venture capitalist Peter Thiel and Vista Equity Partners co-founder Brian Sheth. . . . It was through Sheth, for example, that Scientists to Stop Covid-19 connected with the co-chairman of the Republican National Committee, Thomas Hicks Jr. . . .”
The federal government’s extreme focus on remdesivir has been shaped, in large measure, by the influence of “Scientists to Stop COVID-19”:
1.–“Scientists to Stop Covid-19” is shepherding remdesivir: ” . . . . Scientists to Stop COVID-19 recommends that in this phase, the U.S. Food and Drug Administration (FDA) should work to coordinate with Gilead pharmaceuticals to focus on expediting the results of clinical trials of remdesivir, a drug identified as a potential treatment for COVID-19. The group also recommends administering doses of the drug to patients in an early stage of infection, and notes remdesivir will essentially be a placeholder until a more effective treatment is produced.
2.–The group is doing so by attenuating the regulatory process for coronavirus drugs: “Government entities and agencies appear to adhere to the recommendations outlined by the group, with the Journal reporting that the FDA and the Department of Veterans Affairs (VA) have implemented some of the suggestions, namely relaxing drug manufacturer regulations and requirements for potential coronavirus treatment drugs. . . .”
We conclude discussion of the remdesivir machinations with a piece about the timing of the announcement of Grogan’s departure.
” . . . . Grogan has served as the director of the White House Domestic Policy Council since February 2019, overseeing a broad array of policy issues including health care and regulation. . . . Grogan was one of the original members of the White House coronavirus task force launched in late January. . . . Grogan worked as a lobbyist for drug company Gilead Sciences before joining the Trump administration. . . .”
The departure was announced in the Wall Street Journal on the morning of Wednesday, April 29, the same day we got our first public reports of the NIAID clinical trial of remdesivir that was positive enough to show it shortened the time to recovery and the same day the FDA granted remdesivir emergency use status.
Note, again, the timing of the DSMB’s actions, as well as the influence of “Scientists to Stop Covid-19.”
In FTR #1130, we noted that Moncef Slaoui–formerly in charge of product development for Moderna–was chosen to head Trump’s “Operation Warp Speed.” He will be working with Four-Star General Gustave Perna, chosen by Chairman of the Joint Chiefs of Staff General Mark Milley.
Even after agreeing to sell his Moderna stock, Moncef Slaoui’s investments raise alarming questions–note that he is a “venture capitalist” and a longtime former executive at Glaxo-Smithkline:
The circumstances of his appointment will permit him to avoid scrutiny: ” . . . . In agreeing to accept the position, Dr. Slaoui did not come on board as a government employee. Instead, he is on a contract, receiving $1 for his service. That leaves him exempt from federal disclosure rules that would require him to list his outside positions, stock holdings and other potential conflicts. And the contract position is not subject to the same conflict-of-interest laws and regulations that executive branch employees must follow. . . .”
He will retain a great deal of Glaxo-Smithkline stock: ” . . . . He did not say how much his GSK shares were worth. When he left the company in 2017, he held about [500,000 in Western Print Edition] 240,000 shares and share equivalents, according to the drug company’s annual report and an analysis by the executive compensation firm Equilar. . . .”
Further analysis of Slaoui’s position deepens concern about the integrity of the process: ” . . . . ‘This is basically absurd,’ said Virginia Canter, who is chief ethics counsel for Citizens for Responsibility and Ethics in Washington. ‘It allows for no public scrutiny of his conflicts of interest.’ Ms. Canter also said federal law barred government contractors from supervising government employees. . . . Ms. Canter, a former ethics lawyer in the Obama and Clinton administrations, the Securities and Exchange Commission and other agencies, pointed out that GSK’s vaccine candidate with Sanofi could wind up competing with other manufacturers vying for government approval and support. ‘If he retains stock in companies that are investing in the development of a vaccine, and he’s involved in overseeing this process to select the safest vaccine to combat Covid-19, regardless of how wonderful a person he is, we can’t be confident of the integrity of any process in which he is involved,’ Ms. Canter said.In addition, his affiliation with Medicxi could complicate matters: Two of its investors are GSK and a division of Johnson & Johnson, which is also developing a potential vaccine. . . .”
Next, we turn to Moderna’s animal trial for the messenger RNA vaccine it is developing. There are several considerations to be weighed in connection with the Moderna vaccine.
1.–Again, the chairman of Trump’s “Warp Speed” vaccine development program–Moncef Slaoui–was in charge of Moderna’s product development operation.
2.–Moderna’s trial with mice was positive with regard to generating antibody levels high enough to prevent ADE.
3.–Antibody Dependent Enhancement (ADE), is a phenomena where low levels of ineffective antibodies latch onto the virus and exacerbate an overactive immune response that leads to the deadliest symptoms likes cytokine-storms. This danger was seen with SARS and attempts to create a SARS vaccine so it’s a reasonable fear with SARS-CoV‑2.
4.–The Phase III (human) trial is going to be started in July, involving 30,000 people. Alarmingly, those 30,000 people will all be receiving the exact same dosage, 100 micrograms, and that means the phase III trial won’t be testing sub-optimal dosages. The big Phase III trial won’t be testing for ADE in humans.
5.–We may have a nightmare situation where political pressure gives undo weight to animal safety results, leapfrogging over the necessity of testing for side effects.
6.–The animal trials have been severely criticized: ” . . . . ‘This is the barest beginning of preliminary information,’ said Dr. Gregory Poland, an immunologist and vaccine researcher at the Mayo Clinic who has seen the paper, which has yet to undergo peer-review. Poland said the paper was incomplete, disorganized and the numbers of animals tested were small. . . . Poland, who was not involved with the research, said the paper leaves out ‘important parameters’ that could help scientists judge the work. . . .”
7.–We MIGHT create a vaccine that protects those who get a strong immune response while endangering those with sub-protective responses–a “eugenic” vaccine.
8.–The animal trials have been severely criticized: ” . . . . ‘This is the barest beginning of preliminary information,’ said Dr. Gregory Poland, an immunologist and vaccine researcher at the Mayo Clinic who has seen the paper, which has yet to undergo peer-review. Poland said the paper was incomplete, disorganized and the numbers of animals tested were small. . . . Poland, who was not involved with the research, said the paper leaves out ‘important parameters’ that could help scientists judge the work. . . .”
9.–The phase II clinical trials on humans are still underway and won’t be completed before November. Phase III is going to be getting underway in July. The Human clinical trials are already underway at the same time the animal safety trials have yet to be completed.
10.–Side effects can take a while to manifest.
We provided detailed critical comments on Moderna’s Phase I trial in FTR #1132.
We conclude with a New York Times article sets forth a “Vaccine October Surprise” scenario for this fall.
” . . . . In a desperate search for a boost, he could release a coronavirus vaccine that has not been shown to be safe and effective as an October surprise. Oct. 23, 2020, 9 a.m., with 10 days before the election, Fox New releases a poll showing President Trump trailing Joe Biden by eight percentage points. Oct. 23, 2020, 3 p.m., at a hastily convened news conference, President Trump announces that the Food and Drug Administration has just issued an Emergency Use Authorization for a coronavirus vaccine. Mr. Trump declares victory over Covid-19, demands that all businesses reopen immediately and predicts a rapid economic recovery. Given how this president has behaved, this incredibly dangerous scenario is not far-fetched. In a desperate search for a political boost, he could release a coronavirus vaccine before it had been thoroughly tested and shown to be safe and effective. . . .”
We begin by Introducing the topic of Moderna’s SARS Cov‑2 vaccine as a money maker for both Moderna and as a driver for the market as a whole, we note last Monday’s announcement which generated a major boost in the value of Moderna’s stock and a strong, general rally. The latter apparently stems from optimism that a sucessful vaccine will alleviate the economic damage from Covid-19.
A MarketWatch piece about the rapid fluctuation of Moderna’s stock underscores the significance of the timing of an announcement casting Moderna’s vaccine trial in overly optimistic light:
1.–Moderna’s CEO (Stephen Bancel) and CFO (Lorence Kim) both sold stock on Friday, in accordance with prearranged transactions. Bear in mind, that (as discussed in FTR #1130) Moderna’s stock was trading at $23.46 at the beginning of the year, and the company–which has never marketed a vaccine–was the beneficiary of $483 million dollars in federal funding earlier in the year.) ” . . . . On Friday, Bancel sold 11,046 shares at a weighted average price of $65.56 for about $724,200, as part of a predetermined trading plan adopted Dec. 28, 2018, according to a Form 4 filing with the Securities and Exchange Commission. He also disposed of 1,577 shares as part of a ‘bona fide’ gift. . . . Also, on Friday, Kim sold 20,000 shares at a weighted average price of $65.53 for about $1.31 million, as part of a predetermined trading plan. . . .”
2.–Kim also simultaneously bought and sold shares of his firm for a net profit of $16.79 million on Monday, the day of an overly optimistic announcement by Moderna. The fortuitously timed Moderna announcement made the firm’s CFO roughly $4 million: ” . . . . On Monday, he [Kim] exercised options to buy 241,000 shares at a weighted average price of $12.45 for about $3 million, also as part of a predetermined plan. At the same time, Kim executed sales of 241,000 shares, at a weighted average price of $82.12 for about $19.79 million. That means Kim netted about $16.79 million on the simultaneous buy and sale of shares. . . . with Monday’s stock price surge following the announcement of early data on its vaccine candidate potentially adding $4 million to Kim’s coffers. . . .”
3.–The above-referenced announcement by Moderna led to a dramatic increase in Moderna’s stock and boosted the market as a whole. Moderna announced that evening that it would sell $1.34 billion in stock to help its vaccine operation: ” . . . . Shares of Moderna closed at a record high of $80.00 on Monday after the company released a slice of positive interim clinical data from the first phase of its COVID-19 vaccine trial. That night it announced it would sell $1.34 billion in stock to help fund manufacturing costs associated with the experimental COVID-19 vaccine. . . .”
4.–Moderna’s stock nosedived at the end of the trading day on Tuesday, due to a critical article from Stat News: ” . . . . The stock took a nose dive on Tuesday, closing at $71.67, likely due in some degree to a Stat News story that questioned a lack of clinical clarity in the data it provided to investors. . . .”
Moderna’s announcement was critically assessed by Stat News, which pointed out that the results were incomplete at best: ” . . . . In a clinical-trial data disclosure on Monday, Moderna shared that eight out of 45 participants in its COVID-19 vaccine study developed neutralizing antibodies, a decision that Stat’s Helen Branswell described as a ‘reason for caution.’ It didn’t share information about the immune response to the experimental vaccine in the remaining 37 participants. . . .”
5.–Nonetheless, Moderna’s stock–bolstered by government investment–has been on a dramatic upward swing: ” . . . . The company’s stock was up 3.8% in trading on Wednesday. Year-to-date, it has soared 270.2%, even though the company has no approved products. . . .”
There are serious questions about the substance of Moderna’s statement:
1.–Moderna’s much touted report on its vaccine—which triggered an upsurge in the markets on Monday—appears to have been incomplete, at best, and purposefully deceptive, at worst. “ . . . . While Moderna blitzed the media, it revealed very little information — and most of what it did disclose were words, not data.. . . . If you ask scientists to read a journal article, they will scour data tables, not corporate statements. With science, numbers speak much louder than words. Even the figures the company did release don’t mean much on their own, because critical information — effectively the key to interpreting them — was withheld. . . .”
2.–Part of the reason for alarm and skepticism concerns the behavior of the NIAID—whose director is Anthony Fauci: “ . . . . The National Institute for Allergy and Infectious Diseases has partnered with Moderna on this vaccine. Scientists at NIAID made the vaccine’s construct, or prototype, and the agency is running the Phase 1 trial. This week’s Moderna readout came from the earliest of data from the NIAID-led Phase 1. NIAID doesn’t hide its light under a bushel. The institute generally trumpets its findings, often offering director Anthony Fauci . . . or other senior personnel for interviews. But NIAID did not put out a press release Monday and declined to provide comment on Moderna’s announcement. . . .”
3.–To begin with, Moderna’s announcement was only statistically substantive for 8 of the 45 volunteer subjects: “ . . . . The company’s statement led with the fact that all 45 subjects (in this analysis) who received doses of 25 micrograms (two doses each), 100 micrograms (two doses each), or a 250 micrograms (one dose) developed binding antibodies. Later, the statement indicated that eight volunteers — four each from the 25-microgram and 100-microgram arms — developed neutralizing antibodies. Of the two types, these are the ones you’d really want to see. We don’t know results from the other 37 trial participants. . . .”
4.–It is possible that neutralizing antibodies may have been developed in the 37 test subjects whose data was not released because the testing process is exacting. Still the statement warrants caution, at the least. “ . . . . This doesn’t mean that they didn’t develop neutralizing antibodies.Testing for neutralizing antibodies is more time-consuming than other antibody tests and must be done in a biosecurity level 3 laboratory. Moderna disclosed the findings from eight subjects because that’s all it had at that point. Still, it’s a reason for caution . . . .”
5.–In addition, the age of the subjects was not released and that is relevant. “ . . . . Separately, while the Phase 1 trial included healthy volunteers ages 18 to 55 years, the exact ages of these eight people are unknown. If, by chance, they mostly clustered around the younger end of the age spectrum, you might expect a better response to the vaccine than if they were mostly from the senior end of it. And given who is at highest risk from the SARS-CoV‑2 coronavirus, protecting older adults is what Covid-19 vaccines need to do. . . .”
6.–In addition, there was no data released as to the durability of the neutralizing antibodies. If, for the sake of argument, they are not long-lasting, the utility of the vaccine is negligible. “ . . . . The report of neutralizing antibodies in subjects who were vaccinated comes from blood drawn two weeks after they received their second dose of vaccine. Two weeks. ‘That’s very early. We don’t know if those antibodies are durable,’ said Anna Durbin, a vaccine researcher at Johns Hopkins University. . . .”
7.–Still another point of contention/alarm concerns the variability in neutralizing antibodies among recovered patients: “ . . . . But studies have shown antibody levels among people who have recovered from the illness vary enormously; the range that may be influenced by the severity of a person’s disease. John ‘Jack’ Rose, a vaccine researcher from Yale University, pointed STAT to a study from China that showed that, among 175 recovered Covid-19 patients studied, 10 had no detectable neutralizing antibodies. Recovered patients at the other end of the spectrum had really high antibody levels. So though the company said the antibody levels induced by vaccine were as good as those generated by infection, there’s no real way to know what that comparison means. . . .”
8.–It is less than encouraging that Moderna disclosed that more relevant data will be disclosed in a report to be released in conjunction with NIAID: “ . . . . STAT asked Moderna for information on the antibody levels it used as a comparator. The response: That will be disclosed in an eventual journal article from NIAID, which is part of the National Institutes of Health. . . .”
9.–Ann Durbin was struck by the wording of Moderna’s release: “ . . . . Durbin was struck by the wording of the company’s statement, pointing to this sentence: ‘The levels of neutralizing antibodies at day 43 were at or above levels generally seen in convalescent sera.’ ‘I thought: Generally? What does that mean?’ Durbin said. Her question, for the time being, can’t be answered. . . .”
10.–Jack Rose commented on the opaque nature of Moderna’s release: “. . . . Rose said the company should disclose the information. ‘When a company like Moderna with such incredibly vast resources says they have generated SARS‑2 neutralizing antibodies in a human trial, I would really like to see numbers from whatever assay they are using,’ he said. . . .”
10.–To date, Moderna issues press releases, not papers that can be vetted by the scientific community: “ . . . . It doesn’t publish on its work in scientific journals. What is known has been disclosed through press releases. That’s not enough to generate confidence within the scientific community. ‘My guess is that their numbers are marginal or they would say more,’ Rose said about the company’s SARS‑2 vaccine, echoing a suspicion that others have about some of the company’s other work. ‘I do think it’s a bit of a concern that they haven’t published the results of any of their ongoing trials that they mention in their press release. They have not published any of that,’ Durbin noted. . . .”
After summarizing a highly technical article warning that of the possible consequences of introducing a SARS Cov‑2 vaccine that generates inadequately high levels of antibodies, we detail a 2016 STAT News article about Moderna highlights a number of areas of concern, given the speed and relatively opaque nature of the potential introduction of its Covid-19 vaccine.
The financing of the company by DARPA, and Moncef Slaoui’s joining with Four Star General Perna (elevated by the Chairman of the Joint Chiefs of Staff, General Mark A. Milley) are of additional concern.
1.–As of 2016, Moderna had the largest valuation of any private biotech firm and former employees felt that Moderna prized money over science. Note that, as will be reviewed later in the program, its stock has risen exponentially as a result of the injection of hundreds of millions of dollars. Bear in mind that Moderna has also been underwritten by DARPA. “ . . . . Moderna is worth more than any other private biotech in the US, and former employees said they felt that Bancel prized the company’s ever-increasing valuation, now approaching $5 billion, over its science. . . .”
2.–Moderna has maintained a culture of secrecy, which in 2016, applied to the first two products undergoing phase 1 trials: “ . . . . Moderna just moved its first two potential treatments — both vaccines — into human trials. In keeping with the culture of secrecy, though, executives won’t say which diseases the vaccines target, and they have not listed the studies on the public federal registry, ClinicalTrials.gov. Listing is optional for Phase 1 trials, which are meant to determine if a drug is safe, but most companies voluntarily disclose their work. . . .”
3.–Protein therapy has been a driving economic and therapeutic factor in the pharmaceutical business: “ . . . . For decades, companies have endeavored to craft better and better protein therapies, leading to new treatments for cancer, autoimmune disorders, and rare diseases. Such therapies are costly to produce and have many limitations, but they’ve given rise to a multibillion-dollar industry. The anti-inflammatory Humira, the world’s top drug at $14 billion in sales a year, is a shining example of protein therapy. . . .”
4.–Moderna aims at doing an end run around that technology with the injection of mRNA (messenger RNA) or DNA. This is a risky technology: “ . . . . Moderna’s technology promised to subvert the whole field, creating therapeutic proteins inside the body instead of in manufacturing plants. The key: harnessing messenger RNA, or mRNA. . . . . It’s highly risky. Big pharma companies had tried similar work and abandoned it because it’s exceedingly hard to get RNA into cells without triggering nasty side effects. . . . .”
5.–CEO Bancel has maintained the company’s culture of secrecy: “ . . . . Under Bancel, Moderna has been loath to publish its work in Science or Nature, but enthusiastic to herald its potential on CNBC and CNN, taking part in segments on the world’s most disruptive companiesand the potential “cure for cancer.” . . .”
6.–Moderna had draconian attitude toward employees from its inception: “ . . . . From the beginning, Bancel made clear that Moderna’s science simply had to work. And that anyone who couldn’t make it work didn’t belong. The early Moderna was a chaotic, unpredictable workplace, according to former employees. One recalls finding himself out of a job when a quick-turnaround experiment failed to pan out. Another helped train a group of new hires only to realize they were his replacements. . . .”
7.–Joe Bolen exemplified the treatment Moderna meted out: “ . . . . Most stunning to employees was the abrupt departure of Joseph Bolen, who came aboard in 2013 to lead Moderna’s R&D efforts. Bolen was a big-name hire in biotech circles, an experienced chief scientific officer who had guided Millennium Pharmaceuticals to FDA approval for a blockbuster cancer drug. . . ‘No scientist in his right mind would leave that job unless there was something wrong with the science or the personnel,” said a person close to the company at the time.’ . . .”
8.–Bolen had company: “ . . . . Bolen wasn’t alone. Chief Information Officer John Reynders joined in 2013 to make Moderna what he called the world’s “first fully digital biotech,”only to step down a year later. Michael Morin, brought in to lead Moderna’s scientific efforts in cancer in 2014, lasted less than 18 months. As did Greg Licholai, hired in 2015 to direct the company’s projects in rare diseases. The latter two key leadership positions remain unfilled. . . .”
9.–The explanation of CFO Lorence Kim is less than reassuring from the standpoint of product safety and reliability: “ . . . . ‘We force everyone to grow with the company at unprecedented speed,’ Moderna Chief Financial Officer Lorence Kim said. ‘Some people grow with the company; others don’t.’ . . .”
10.–Beginning in 2013, Moderna partnered with a series of pharmaceutical giants, including AstraZeneca, which has been selected to develop a Covid-19 vaccine: “ . . . . That’s when Moderna — which had just 25 employees — signed a staggering $240 million partnership with UK pharmaceutical giant AstraZeneca. It was the most money pharma had ever spent on drugs that had not yet been tested in humans. . . .”
11.–The firm has been lavishly capitalized: “ . . . . In early 2015, Moderna disclosed a $450 million financing round, the largest ever for a private biotech company. This month, the company broke its own record, raising another $474 million. . . . Though it has yet to reveal data from a single clinical trial, Moderna is now valued at $4.7 billion, according to Pitchbook. . . .”
12.–Initially, Moderna aimed at developing products that would be administered for a period of years: “ . . . . From the start, Moderna heralded its ability to produce proteins within cells, which could open up a world of therapeutic targets unreachable by conventional drugs. The most revolutionary treatments, which could challenge the multibillion-dollar market for protein therapy, would involve repeated doses of mRNA over many years, so a patient’s body continued to produce proteins to keep disease at bay. . . .”
13.–Instead of producing treatments that would be administered over a period of years, the company focused on vaccines: “ . . . . But Moderna’s first human trials aren’t so ambitious, focusing instead on the crowded field of vaccines, where the company has only been working since 2014. . . . The choice to prioritize vaccines came as a disappointment to many in the company, according to a former manager. The plan had been to radically disrupt the biotech industry, the manager said, so ‘why would you start with a clinical program that has very limited upside and lots of competition?’” . . . .”
14.–The answer to Moderna’s focus on vaccines may be due to issues of product safety: “ . . . Delivery — actually getting RNA into cells — has long bedeviled the whole field. On their own, RNA molecules have a hard time reaching their targets. They work better if they’re wrapped up in a delivery mechanism, such as nanoparticles made of lipids. But those nanoparticles can lead to dangerous side effects, especially if a patient has to take repeated doses over months or years. . . .”
15.–Vaccines will only administer mRNA at the time of vaccination, rather than over a long period of time: “ . . . . ‘I would say that mRNA is better suited for diseases where treatment for short duration is sufficiently curative, so the toxicities caused by delivery materials are less likely to occur,’ said Katalin Karikó, a pioneer in the field who serves as a vice president at BioNTech. . . That makes vaccines the lowest hanging fruit in mRNA, said Franz-Werner Haas, CureVac’s chief corporate officer. ‘From our point of view, it’s obvious why [Moderna] started there,’ he said.’ . . .”
16.–Moderna’s explanation for its focus on vaccines is not reassuring—the speed with which it can proceed to human trials. The firm’s secrecy has generated alarm: “ . . . . Moderna said it prioritized vaccines because they presented the fastest path to human trials, not because of setbacks with other projects. ‘The notion that [Moderna] ran into difficulties isn’t borne in reality,’ said Afeyan. But this is where Moderna’s secrecy comes into play: Until there’s published data, only the company and its partners know what the data show. Everyone outside is left guessing — and, in some cases, worrying that Moderna won’t live up to its hype. . . .”
17.–Moderna applies software and a business model derived from Tesla, Amazon and Uber: “ . . . . Moderna has pioneered an automated system modeled on the software Tesla uses to manage orders, Bancel said: Scientists simply enter the protein they want a cell to express, and testable mRNA arrives within weeks. . . . That has always been part of the plan, former employees said, pointing to Bancel’s fascination with the tech industry. Uber and Amazon were not the first to come up with their respective business ideas, but they were the ones that built enough scale to ward off competition. And Moderna is positioning itself to do the same in mRNA. . . .”
Moncef Slaoui’s optimistic statement on the Friday before the Monday announcement, presents important context for Moderna’s Monday announcement. That announcement moved markets based on inadequate data. “Operation Warp Speed” (headed by Slaoui) suggests that candidate Trump is very interested in those preliminary results as well.
Elizabeth Warren scored Slaoui’s conflict of interest–a consideration that will be discussed at length: ” . . . . Following Moncef Slaoui’s Friday appointment as a co-leader of the Warp Speed program, he’s set to sell about 155,000 shares in Moderna, according to press reports. They were worth an estimated $10 million Friday, but after Monday’s stock run-up on positive early data, they’re now valued at about $12.4 million. . . . Following Slaoui’s selection, Sen. Elizabeth Warren tweeted that it’s a ‘huge conflict of interest’ for him to keep the Moderna stock as he assumes the new role. She said he should ‘divest immediately.’ In a now-deleted tweet, Slaoui responded that there ‘is no conflict of interest, and there never has been,’ Business Insider reports. . . .”
Even after agreeing to sell his Moderna stock, Slaoui’s investments raise alarming questions–note that he is a “venture capitalist” and a longtime former executive at Glaxo-Smithkline:
1.–The circumstances of his appointment will permit him to avoid scrutiny: ” . . . . In agreeing to accept the position, Dr. Slaoui did not come on board as a government employee. Instead, he is on a contract, receiving $1 for his service. That leaves him exempt from federal disclosure rules that would require him to list his outside positions, stock holdings and other potential conflicts. And the contract position is not subject to the same conflict-of-interest laws and regulations that executive branch employees must follow. . . .”
2.–He will retain a great deal of Glaxo-Smithkline stock: ” . . . . He did not say how much his GSK shares were worth. When he left the company in 2017, he held about [500,000 in Western Print Edition] 240,000 shares and share equivalents, according to the drug company’s annual report and an analysis by the executive compensation firm Equilar. . . .”
3.–Further analysis of Slaoui’s position deepens concern about the integrity of the process: ” . . . . ‘This is basically absurd,’ said Virginia Canter, who is chief ethics counsel for Citizens for Responsibility and Ethics in Washington. ‘It allows for no public scrutiny of his conflicts of interest.’ Ms. Canter also said federal law barred government contractors from supervising government employees. . . . Ms. Canter, a former ethics lawyer in the Obama and Clinton administrations, the Securities and Exchange Commission and other agencies, pointed out that GSK’s vaccine candidate with Sanofi could wind up competing with other manufacturers vying for government approval and support. ‘If he retains stock in companies that are investing in the development of a vaccine, and he’s involved in overseeing this process to select the safest vaccine to combat Covid-19, regardless of how wonderful a person he is, we can’t be confident of the integrity of any process in which he is involved,’ Ms. Canter said. In addition, his affiliation with Medicxi could complicate matters: Two of its investors are GSK and a division of Johnson & Johnson, which is also developing a potential vaccine. . . .”
Moderna stands to make billions of dollars if their vaccine goes to market:
1.–” . . . . What investors are betting on, for Moderna and others developing vaccines against the SARS-CoV‑2 virus, is that a third of the developed world’s population will get vaccinated every year. That could amount to a $10 billion annual business, at an estimated price of $30 per vaccination. . . .”
2.–” . . . . Morgan Stanley analysts this past weekend suggested that pricing might start at $5 to $10 a dose during this first pandemic crisis, then rise to a range of $13 to $30 for preventive doses in future years. But at BMO Capital Markets, analyst George Farmer speculated that Moderna could start charging $125 per treatment in the U.S. market and raise that price over time to $200. . . . ”
We close the program with a reminder of the extent to which federal funding drives the value of Moderna: ” . . . . ‘Instead of waiting for the data and then scaling up with manufacturing process … we can make as many doses as we can. We are doing both in parallel,’ he said. The company plans to hire up to 150 people to support the effort. Bancel said the company ‘couldn’t have done this’ without the funding commitment from the Biomedical Advanced Research and Development Authority, which is part of the Department of Health and Human Services. . . .”
In this program, we highlight the disconcerting CV’s of Saikat Chakrabarti, Cenk Uygur, Alexandria Ocasio-Cortez, as well as PACs and related entities created by Chakrabarti and underpinning AOC. Chakrabarti appears to be a political acolyte of Subhas Chandra Bose, “The Duce of Bengal.” In a YouTube segment defending AOC against criticism, the recently resigned Chakrabarti sported a T‑shirt featuring the likeness of that key Indian fascist.
“Subhas Chandra” Chakrabarti ignited the war within the Democratic Party that he had intended. Noteworthy in his “funky resume” is the fact that he worked for Bridgewater Associates, the world’s largest hedge fund. James Comey was the firm’s chief legal counsel, before moving to head the FBI. His reopening of the Hillary Clinton e‑mail “non-scandal” just before election day helped give Trump the victory.
Following his resignation this past week, “Subhas Chandra” Chakrabarti is now under investigation for his campaign finance activities: ” . . . The inquiry centers on two political action committees founded by Saikat Chakrabarti . . . . The two PACs being probed, Brand New Congress and Justice Democrats, were both set up by Chakrabarti to support progressive candidates across the country. . . . But they funneled more than $1 million in political donations into two private companies that Chakrabarti also incorporated and controlled, according to Federal Election Commission filings and a complaint filed in March with the regulatory agency. In 2016 and 2017, the PACs raised about $3.3 million, mostly from small donors. A third of the cash was transferred to two private companies whose names are similar to one of the PACs — Brand New Congress LLC and Brand New Campaign LLC — federal campaign filings show. . . .”
We suspect that the irregularities in Chakrabarti’s activities and the irregularities in Ocasio-Cortez’s resume and activities were not only deliberately preconceived, but are part of an electoral “Psy-Op” that will get considerable coverage in the 2020 campaign, possibly handing victory to Trump.
“Team AOC” will of, course, cry “racism” via Twitter.
AOC has already been handed Martyr Status by Donald Trump’s attacks, and we believe she may well become the face of the Democratic Party, as Team Trump wishes.
A blog post from “The Medium” notes the fishy elements of AOC’s CV, the questionable activities of the Chakrabarti entities and the indications that “Team AOC” has more in common with the very right-wing elements and individuals that they decry than anything that could be called “progressive:” ” . . . . independent research into her background and funding has revealed ‘Democratic Socialist’ Ocasio-Cortez is neither a progressive Democrat nor a good faith candidate. And for someone with an economics degree — one of the only claims on her resume that checks out — the 28-year-old candidate has a lot to learn about campaign finance and election law. At any other time, Ocasio-Cortez’ myriad red flags — her unlikely victory, antagonistic rhetoric, national amplification, and shady funding — would beg media scrutiny. . . .This new breed of supposed “progressives” — with their radicalized, anti-establishment fervor — appear to have more in common with that far-right insurgency [the Tea Party] than either group has with mainstream American politics. . . . But we are not living in ordinary times — a situation Ocasio-Cortez and her “progressive” posse are all too willing to exploit to accomplish their destructive goals. As natural as any evolution, the “Bernie or Bust” influence operation that infected our 2016 election is alive, well, and adapted for survival. It’s new useful idiots are Ocasio-Cortez and the murky entanglement of two new Political Action Committees (PACs)— founded by The Young Turks’ scandal-plagued host Cenk Uygur and a group of tech-savvy ex-Bernie campaign staffers. . . .”
Questionable aspects of Team AOC include:
1.–Her entrepreneurial pretense, which appears to be illusory.
2.–Her elevation of undergraduate/internship activities to be political posts.
3. –The dubious fabric of her Bronx working class cache: ” . . . . Ocasio-Cortez has claimed to be a ‘third-generation Bronxite’ from a ‘working class’ family. . . . She graduated from the predominately white Yorktown High School located in Yorktown Heights, NY, where the average household income is $141,254 and average household net worth is $1,192,838. . . .”
4.–The fact that she appears to have vetted herself as a candidate: ” . . . . A review of the core staff reveals significant crossover and a musical chairs of board members between the two [PACs]. Ocasio-Cortez assumed a leadership role with Justice Democrats sometime in 2017 — thereby effectively vetting herself for the role of candidate. . . .”
5.–Brand New Congress recruiting candidates to run as Republicans in red districts: ” . . . . Brand New Congress, the PAC we now see Ocasio-Cortez criss-crossing the country helping to promote, has the perplexing mission of ‘attempting to recruit Congressional candidates to run as Republicans in red districts.’ . . .”
6.–The contradictory nature of Team AOC’s activities is encapsulated in the following analytical synopsis: ” . . . . An analysis of FEC filings shows that their network of PACs, LLCs, board and staff navigate in the same legal and ethical grey area their entire “anti-dark money” platform is based on combatting. Beginning with Justice Democrats, the PAC has raised $2,100,399 over the course of the 2017–2018 election season. Yet over that same time period, the PAC has made zero independent expenditures in support of any candidates. In fact, dozens of candidates have instead made payments to Justice Democrats. . . .”
7.–The central role of the “Bernie Bots” in this unsavory activity: ” . . . . A review of disbursements reveals that of the $2,026,298 spent to date, over $600,000 for “strategic consulting” services was directed to Brand New Congress LLC — a business entity controlled by Chakrabarti. Another $1 million in contributions has been directed to ex-Bernie staffers or their firms. This includes $222,000 to Middle Seat Consulting LLC, run by Brand New Congress co-Founder Zack Exley, and about $800,000 in salaries and payroll costs. Because those LLCs have not disclosed financial reports, the public has no way of knowing what that money was used for. . . .”
8.–Brand New Congress also benefiting the Bernie Bots: ” . . . . A review of Brand New Congress PAC filings demonstrate a similar movement of fundraising donations into the pockets of ex-Bernie “consultants”. Of the $477,688 raised, no independent expenditures to candidates were made, yet $261,000 was paid to Brand New Congress LLC and over $100,000 was disbursed as salaries or payroll costs. . . .”
Program Highlights Include:
1.–Review of key points of the fascist activities of “Team Bose.”
2.–Review of Narendra Modi’s fushion of Hindutva fascism with Team Bose.
3.–An overview of Cenk Uygur’s curious resume.
9.–A constellation of highly questionable activities in connection with AOC’s defeat of 10-term Congressman Joe Crowley, such as the role of the “Blue America” PAC, UK English copy: ” . . . . The meme-heavy social media pages for the PAC’s various websites pushed out vitriolic blog and social media posts during the primary, using budget graphics with British-English copy to promote hashtags like #AbolishICE #Berniewouldhavewon and #MobBossCrowley. . . .”
Program Highlights Include:
Review of key points of the fascist activities of “Team Bose.”
Review of Narendra Modi’s fushion of Hindutva fascism with Team Bose.
An overview of Cenk Uygur’s curious resume.
There was an ominous warning about the direction American Democracy was heading When David Frum warned, “If conservatives become convinced that they cannot win democratically, they will not abandon conservatism. They will reject democracy.” It was a warning about what might happen, but as we’re going to see, the corporate/billionaire wing component of the Republican party has already concluded that it can’t get the public behind its agenda and has already turned against democracy. And John Roberts just handed this billionaire faction a massive legal victory in Rucho vs Common Cause: federal courts can’t rule on whether or not district lines are drawn in an overly-partisan manner. It’s up to each state on its own. And as we’re going to see, Republicans already dominate the control of state governments and now state legislatures can gerrymander their own districts without fear of federal meddling. Beyond that, the Kochs and ALEC are working on removing state courts from overseeing redistricting maps too. And to top it off, the Kochs are aggressively pushing for a constitutional convention that could easily turn into a ‘runaway’ convention. And if there’s a constitutional convention, whichever party controls the most states is going to control the outcome of the convention. So the Supreme Court just turbocharged the Kochs’ capture of state assemblies, the House of Representatives, and eventually the Constitution.