Concluding the discussion contained in part of FTR #1147 and all of FTR #1148, we finish the presentation of a very important article by the brilliant Peter Dale Scott, written almost 35 years ago. With the GOP convention in full swing as these programs were being recorded, the symbiosis between Allen Dulles and the Nazi SS is fundamental to understanding not only the genesis of the U.S. intelligence establishment, but how that institution is inextricably linked with the Republican Party.
The link to this article permits the listener/reader to download (for free) the entire issue of Covert Action Quarterly. Mr. Emory strongly recommends that they do so, as the other articles in this excellent issue will supplement the analysis beautifully.
Due to the length and complexity of this article, we are not transcribing it, but will summarize important points of information.
Key Points of Analysis:
1.–Dulles’s negotiations with the SS preceded by months the official story of the contact between U.S. intelligence and the Gehlen team. ” . . . . It is interesting to note that Gehlen knew of Wolff’s contacts with Dulles s early as January 1945, the month in which they were initiated. From this same period he began to consolidate his networks for survival after Hitler’s downfall, which is to say he already expected to reach a modus vivendi with the Americans. In April 1945, one month before the war ended, Dulles asked Frank Wisner to begin talks with Gehlen, who was not taken into U.S. custody until May 20. On the Gehlen side, a plan ‘to gain contact with the Americans’ was approved on April 9. . . .”
2.–Dulles’s negotiations with the SS, involving Walter Rauff–who devised the mobile gas chambers used on the Eastern Front–were conducted as part of Operation Sunrise. ” . . . . Despite the [U.S.] Army interrogator’s pleas that Rauff ‘is considered a menace if ever set free, and failing actual elimination, is recommended for life-long internment,’ Dulles kep his bargain and Rauff was released. According to usually reliable intelligence sources. Dulles then employed Rauff on anti-communist operations in Italy, which was Rauff’s specialty under the Nazis. . . .”
3.–Although the Vatican was deeply involved with the SS/OSS negotiations, Dulles’ team was the primary component. ” . . . It was Dulles’s contacts, not the Vatican, who handled the smuggling of Nazis. According to top secret State Department documents, the Italian police provided the false passports for allied agents; the visas came from the Argentine consulate in the allied intelligence unit based at Trieste;and the embarkation paperwork was handled by a U.S. State Department officer in Genoa. Genoa, incidentally was Rauff’s area of jurisdiction. All of them worked for Dulles. . . .”
Supplementing the information in the Peter Dale Scott article, we present information about Mengele’s work in Paraguay in conjunction with the CIA and Pentagon: ” . . . . In the last named country, the son of a Bavarian cavalry officer, President Stroessner, cooperates with the United States military authorities and the CIA, as he does with Bormann and his representatives. During the Vietnam war, President Stroessner permitted the U.S. Army Chemical Corps and the CIA to send in teams of 2,500 men to carry out field tests, in the Matto Grosso jungle, of chemicals for use in Vietnam. In one instance, several American soldiers became casualties when they accidentally were sprayed with the gas. They were taken to a Paraguayan military field hospital; the doctor who treated them was Josef Mengele, now a Paraguayan citizen and an officer in the Paraguayan Army Medical Corps. Under Mengele’s treatment, all soldiers recovered. None, of course, knew the true identity of their medical benefactor. . . .”
Of paramount importance in the context of this presentation, is the fact that it was William Casey who was in charge of OSS operations in Germany in late 1944 and 1945, as Dulles, Donovan, and the SS were forging their alliance!! This places Casey’s role in the Crusade For Freedom and the derivative Reagan campaign and administration in perspective.
Placing the co-evolution of the Crusade For Freedom, the GOP and the Gehlen “Org” in context, we note that:
1.–The Gehlen organization was a direct extension of the Third Reich’s national security establishment, coalescing with the approval of a German chain of command that was still in effect after the formal conclusion of hostilities.
2.–The OUN/B, Iron Guard, Croatian Ustachis and other Eastern European fascist groups were part of the Gehlen organization. They were the primary elements in the GOP’s Ethnic Heritage Outreach Council.
3.–This places William Casey’s central role in the GOP Nazi branch as an element in the perpetuation of the Third Reich’s national security establishment.
Next, we review analysis of the Crusade For Freedom–the covert operation that brought Third Reich alumni into the country and also supported their guerilla warfare in Eastern Europe, conducted up until the early 1950’s. Conceived by Allen Dulles, overseen by Richard Nixon, publicly represented by Ronald Reagan and realized in considerable measure by William Casey, the CFF ultimately evolved into a Nazi wing of the GOP.
While serving as chairman of the Republican National Committee, the elder George Bush shepherded the Nazi émigré community into position as a permanent branch of the Republican Party.
Note that the rise of the Reagan administration was essentially the ascent of the Nazified GOP, embodied in the CFF milieu. Reagan (spokesman for CFF) was President; George H.W. Bush (for whom CIA headquarters is named) was the Vice President; William Casey (who handled the State Department machinations to bring these people into the United States) was Reagan’s campaign manager and later his CIA director.
Central to understanding the merging of the U.S. with Nazi Germany in an anti-Soviet alliance–is the understanding of what globalization really is and how it precipitated fascism and the Second World War.
Also central to an understanding of the realization of the consummate manifestation of both globalization and fascism/Nazism–is analysis of the machinations of the Bush family. The heroic Justice Department investigator (later author) John Loftus delineated the Bush family’s role in the laundering of Nazi funds between the Thyssen Bank in Berlin, the Bank voor Handel en Scheepvaart, N.V. and the Union Bank in the U.S.
The networking of the Bush family with the Thyssens, and the Rockefellers, in turn, is inextricably linked with the coalescence and operation of the remarkable and deadly Bormann flight capital network, highlighted in FTR #305, among other programs.
Of paramount importance is the role of the two institutions in which Prescott Bush served–Brown Brothers Harriman and the Union Bank–as a fundamental vehicle for laundering money from the consummately powerful Rockefeller family and related interests in Nazi Germany. ” . . . . But what did the Bush family know about their Nazi connection and when did they know it? As senior managers of Brown Brothers Harriman, they had to have known that their American clients, such as the Rockefellers, were investing heavily in German corporations, including Thyssen’s giant Vereinigte Stahlwerke. As noted historian Christopher Simpson repeatedly documents, it is a matter of public record that Brown Brother’s investments in Nazi Germany took place under the Bush family stewardship. . . . It should be recalled that in January 1937, he hired Allen Dulles to ‘cloak’ his accounts. But cloak from whom? Did he expect that happy little Holland was going to declare war on America? The cloaking operation only makes sense in anticipation of a possible war with Nazi Germany. If Union Bank was not the conduit for laundering the Rockefeller’s Nazi investments back to America, then how could the Rockefeller-controlled Chase Manhattan Bank end up owning 31% of the Thyssen group after the war? It should be noted that the Thyssen group (TBG) is now the largest industrial conglomerate in Germany, and with a net worth of more than $50 billion dollars, one of the wealthiest corporations in the world. TBG is so rich it even bought out the Krupp family, famous arms makers for Hitler, leaving the Thyssens as the undisputed champion survivors of the Third Reich. Where did the Thyssens get the start-up money to rebuild their empire with such speed after World War II? . . . . A fortune this size could only have come from the Thyssen profits made from rearming the Third Reich, and then hidden, first from the Nazi tax auditors, and then from the Allies. The Bushes knew perfectly well that Brown Brothers was the American money channel into Nazi Germany, and that Union Bank was the secret pipeline to bring the Nazi money back to America from Holland. The Bushes had to have known how the secret money circuit worked because they were on the board of directors in both directions: Brown Brothers out, Union Bank in. . . .”
Further solidifying the continuity between the Third Reich, the Gehlen Org and the GOP, we note that, while it was the BND (the intelligence service of the Federal Republic) the “Org” was financing the Eastern European fascist groups that were part of the Ethnic Heritage Outreach Council.
Fleshing out information about the BND financing of groups linked to the Anti-Bolshevik Bloc of Nations, we present supplemental information from an unpublished manuscript. The author is well-known to veteran researchers, but will remain anonymous, since the work was never formally completed or published.
Providing background to discussion of the relationship between the milieu of Resorts International, Nixon, his banking associate Bebe Rebozo and William Casey, we note that Rebozo’s banking of funds from the deadly Bormann network, the institution that Mr. Emory feels will prove to be the decisive element on this earth.
Continuing with discussion from the unpublished manuscript referenced above, the broadcast highlights interactions between the Nixon administration, Bebe Rebozo, a mysterious and allegedly organized-crime connected company called Resorts International, an even more mysterious subsidiary of Resorts International called the Paradise Island Bridge Company and the Dewey, Dulles, Nazi, William Casey milieu that is central to this discussion.
Note that Donald Trump was a suitor for the ownership of Resorts International (after the 1986 death of James Crosby), ultimately purchasing the Taj Mahal Casino from the firm after a lawsuit with television star Merv Griffin.
Recorded as the 2020 GOP convention was in full swing against the background of escalating violence in the streets of American cities, these programs set forth history fundamental to the development of the modern GOP and Nazi/SS elements that were incorporated into the foundation of the U.S. intelligence system at the end of World War II. Those elements, in turn, are inextricably linked with the GOP.
Before that discussion, however, the program highlights yet another element in the Wall Street/Third Reich/Swiss political and corporate maneuvering that set the stage for postwar Transatlantic fascism.
Once again, Allen Dulles and his connections are front and center. With Bernie Sanders and AOC garnering rhetorical gravitas from the so-called progressive sector, there has been discussion of former Vice President Henry Wallace and his highly progressive political agenda. The nature of the discussion has centered on Wallace’s political defenestration by what has been termed “the Democratic Party’s Establishment.”
In fact, Wallace’s political demise was due to his own indiscretion. His brother-in-law was Charles Bruggmann, the Swiss ambassador to the United States. With the massive investment in the Swiss economy by Third Reich finance and industry and with key holding companies in Switzerland dominating significant elements of the German-American corporate relationship, Bruggmann had a vested interest in keeping Nazi Germany abreast of U.S. plans and did so through the Abwehr and Allen Dulles.
” . . . . Both organizations received a mass of high-value intelligence via the Swiss ambassador to Washington, Dr. Charles Bruggmann. Yet Bruggmann was no spy: his source was his brother-in-law, Henry Wallace—who happened to be the Vice President of the United States. Wallace was a popular, left-wing New Dealer; privy to many of America’s most important secrets, he was also notoriously indiscreet. . . .”
Allen Dulles
In addition to communicating the Treasury Department’s plans to de-industrialize Germany to prevent future wars, the Bruggmann/Abwehr/Dulles axis was instrumental in betraying Operation Safehaven, the plan to interdict the Nazi flight capital program that crystallized as the Bormann flight capital program.
” . . . . However this effort required the cooperation of OSS agents already on the ground, and in Switzerland this was problematical—since one of the suspects of Operation Safehaven was Allen Dulles himself, because of his extensive corporate connections and his links with various Nazi groups. Despite this difficulty, the investigation necessarily focused on the gold dealings undertaken by Swiss banks. This became of major concern to Swiss ambassador Bruggmann once he learned of Operation Safehaven trough his indiscreet brother-in-law, Vice President Henry Wallace. The exposure of the explicit links between Swiss banks and Nazi Germany would be a major potential embarrassment to the Swiss government once the war over; accordingly the Swiss Secret Service alerted Allen Dulles about the Safehaven investigation into his affairs. . . .”
The rest of FTR #1147 and all of FTR #1148 accesses a very important article by the brilliant Peter Dale Scott, written almost 35 years ago. With the GOP convention in full swing as these programs were being recorded, the symbiosis between Allen Dulles and the Nazi SS is fundamental to understanding not only the genesis of the U.S. intelligence establishment, but how that institution is inextricably linked with the Republican Party.
The link to this article permits the listener/reader to download (for free) the entire issue of Covert Action Quarterly. Mr. Emory strongly recommends that they do so, as the other articles in this excellent issue will supplement the analysis beautifully.
Due to the length and complexity of this article, we are not transcribing it, but will summarize important points of information.
Key Points of Analysis:
1.–Joseph Mengele, the SS “Angel of Death” of Auschwitz infamy, was networked with other SS war criminals who gravitated seamlessly into the service of the Gehlen “Org” and the CIA. His whereabouts were known to U.S. intelligence, who masked them from Nuremberg prosecutors. Background on Mengele, his operational links with the Kaiser Wilhelm Institute and his position in the eugenics milieu, see, among other programs, FTR #‘s 664 and 908. ” . . . . the response of Telford Taylor, U.S. Chief of Counsel for War Crimes at Nuremberg was “to advise our records show Dr. Mengerle [sic] is dead as of October 1946.” (At the time of General Taylor’s letter, U.S. Army Counterintelligence knew both of Mengele’s survival and even his location, in the small Bavarian village of Autenreid.) . . . .”
2.–One of the networks with which Mengele operated was the Estrella firm. ” . . . . Alfons Sassen, the representative of the Brotherhood [Kameradenwerk] Business enterprise known as “Estrella.” It is said too that Sassen is financed by Dr. Josef Mengele, who controls now such funds as remain liquid from the sale of European loot. . . . [Klaus Barbie] set up a company called Estrella, ostensibly dealing in quinquina bark. Although no records exist in the public registry in La Paz, at least one Bolivian arms dealer still remembers it as a weapons trading company. . . .”
3.–Mengele may have been incorporated into the U.S. biological warfare program, although me maintained residence in Latin America. ” . . . . Could Mengele–not even a political policeman (like Rauff and Barbie), but a doctor with a penchant for lethal experiments on human guinea pigs–could even Mengele have been saved s a result of a secret deal between Dulles and the SS? . . . . we have since been told that his colleague in the Auschwitz human experiments, Walter Schreiber, was shielded by the Americans from a Polish conviction in absentia, so that he could help guide the postwar researches of the U.S. Air Force in bacteriological warfare. . . That Mengele’s escape and immunity were arranged by the United States, like those of Schreiber and so many others, will seem more probable once we have studied the incredible postwar careers of [Klaus] Barbie, [Friedrich] Schwend and [Walter] Rauff . . . .”
4.–Allen Dulles’s successful negotiations with the SS were fundamental to his goal of establishing the postwar CIA as a vehicle for the perpetuation of the SS under CIA/Gehlen auspices: ” . . . . But they [Allen Dulles and OSS chief William Donovan] also knew that, just as the OSS was the best hope for the survival of the SS cadres, so in a sense these cadres were their highest trump card in the impending contest for the OSS’s own institutional home for the postwar Gehlen Org. In 1948 Dulles, by now a civilian, helped write the memo persuading Truman to take on the Gehlen Org, on Gehlen’s own terms. . . .”
5.–Dulles’s negotiations with the SS preceded by months the official story of the contact between U.S. intelligence and the Gehlen team.
6.–Dulles’s negotiations with the SS, involving Walter Rauff–who devised the mobile gas chambers used on the Eastern Front–were conducted as part of Operation Sunrise. ” . . . . Despite the [U.S.] Army interrogator’s pleas that Rauff ‘is considered a menace if ever set free, and failing actual elimination, is recommended for life-long internment,’ Dulles kept his bargain and Rauff was released. According to usually reliable intelligence sources. Dulles then employed Rauff on anti-communist operations in Italy, which was Rauff’s specialty under the Nazis. . . .”
7.–Although the Vatican was deeply involved with the SS/OSS negotiations, Dulles’ team was the primary component. ” . . . It was Dulles’s contacts, not the Vatican, who handled the smuggling of Nazis. According to top secret State Department documents, the Italian police provided the false passports for allied agents; the visas came from the Argentine consulate in the allied intelligence unit based at Trieste;and the embarkation paperwork was handled by a U.S. State Department officer in Genoa. Genoa, incidentally was Rauff’s area of jurisdiction. All of them worked for Dulles. . . .”
This series of programs should be digested against the background of a very important development that has not generated much dialogue or attention. A new branch of the military has been created–the Space Force, joining the Army, Navy and Air Force (the Marines are technically part of the Navy.)
As people listen to the discussion of the space plane, this should be borne in mind.
The program begins on an interrogatory note. In numerous programs, we have covered Project HAARP–a military environmental modification technology. HAARP came online a quarter of a century ago, and should be considered in the context of a treaty that was concluded between the U.S. and the former Soviet Union in the 1970s that explicitly banned environmental modification for military purposes.
(Programs featuring information about HAARP include five interviews with Nick Begich: FTR #‘s 1, 30, 79, 101, 128.)
Mr. Emory had been expecting environmental modification warfare to be employed as part of the full-court press against China. That country has been beset by enormous flooding, that some critics see as destabilizing that country’s politics. ” . . . . ‘I believe that the Chinese public will question Beijing from this year’s continuous natural and man-made disasters, and even question China’s governance model and its effectiveness,’ said Wu Qiang, an independent political analyst in Beijing. . . . Of course, microwaves from space could also, potentially, be a weapon. . . . ”
A top secret military project has been underway for years–a space plane that can stay aloft for long periods of time. This development should be seen against the background of Donald Trump’s new Space Force–a novel branch of the military.
It should also be seen against the background of environmental warfare: HAARP came online 25 years ago and the U.S/U.S.S.R treaty was concluded more than forty years ago.
Just consider the advances in military aviation–the Wright brothers flew in 1903. Just look at how far military aviation had advanced by 1928 and, subsequently 1948. It is reasonable to assume that environmental warfare technology has advanced correspondingly.
The space plane is involved with technological advances developed by William Brown of Raytheon and Wernher von Braun, the SS officer and war criminal who headed the American space program. ” . . . . In the 1960s, Brown went on to work with NASA’s Wernher von Braun on converting microwave beams into electrical current. The concept had particular relevance for powering future spacecraft — but also promised a way to harness the power of sunlight, up to 10 times more potent above the atmosphere and its dust, for use on earth. . . Of course, microwaves from space could also, potentially, be a weapon. . . . the U.S. Air Force revealed some of the satellite payloads and experiments it will carry aloft this month [May of 2020], including one that will try converting the sun’s energy into a form that can be sent to Earth . [Such as lightning strikes?–D.E.] . . .”
Mr. Emory notes that, in early 2020, the space plane concluded a long, classified mission of more than a year in duration. Shortly after, Northern California experienced the first February on record with no rainfall at all–and this after what had been a normal rainy season.
After Northern California was bombarded with lightning strikes, the Bay Area was enveloped with record wildfires, experiencing some of the worst air quality in the world. This prompted several points of inquiry:
1.–Might the total absence of rainfall in February and, perhaps, the highly unusual number of lightning strikes be linked to the space plane and advances in environmental warfare?
2.–With Covid-19’s effects exacerbated by dirty air, might this be a harbinger of a dramatic worsening of the Pandemic in the fall?
3.–Might the space plane and advances in environmental warfare be involved in China’s record flooding?
4.–The space plane’s missions are opaque: ” . . . . [Secure World Foundation’s Brian] Weeden’s main concerns about the X‑37B are that it puts stuff in space and doesn’t tell anyone. ‘On the previous mission they deployed three small satellites from the X‑37B and didn’t even catalog them until after it had landed and those satellites had decayed from orbit,’ he said. ‘That’s the sort of non-transparent and potentially irresponsible behavior the U.S. has criticized the Russians and Chinese for in the past.’ . . .”
Mr. Emory’s musings should also be considered in the context of the thesis set forth in L‑2.
Much of the program details the incorporation of the Nazi rocket program’s military commander–Walter Dornberger–and SS Major Wernher von Braun into the U.S. V‑2 program Project Hermes (contracted for by General Electric in November of 1944.)
Dornberger and von Braun were in touch with G.E. in December of 1944, months before the surrender of Nazi Germany! They subsequently went to work for G.E. and Project Hermes!
Key points of analysis and discussion include:
1.–The overwhelming probability that the G.E./Dornberger/von Braun liaison was arranged on the German end by SS General Hans Kammler, who had overall supervisory control of the Nazi rocket program.
2.–The probability that the arrangements were facilitated in Lisbon by Sigismund von Braun–the brother of Wernher von Braun and an agent for the SD. The Sichereitsdienst (SD) was the SS intelligence service.
3.–The probability that Sigismund von Braun’s Lisbon sojourn and arrangement for the G.E./Dornberger/von Braun liaison was also facilitated by Ernst von Weiszacker, Nazi Germany’s ambassador to the Vatican.
Subsequent programs in this series will center on OSS agent and Sullivan & Cromwell attorney Allen Dulles’s treasonous liaison with the Nazi SS and collaboration with the Vatican to incorporate the SS into the The Gehlen “Org” and the CIA.
In all probability, it was Allen Dulles who established contact with Kammler/Dornber and the von Braun brothers, also with probable Vatican complicity.
In FTR #511, we noted that AEG–German General Electric (which made electrical components for the V‑2)–was 30% owned by American G.E. General Electric was not only a client of Sullivan & Cromwell, but was formed by it.
Program Highlights Include:
1.–Review of Sullivan & Cromwell’s decisive position in the American corporate pantheon.
2.–Review of Wernher von Braun’s work for the SS and the fact that he was a war criminal.
3.–Review of Allen Dulles’s treasonous dealings with Prince Max Egon von Hohenlohe–an emissary of SD foreign intelligence chief Walter Schellenberg.
Fleshing out the deep politics underlying the life and death of Park Won-soon, this program builds on the foundation of first two programs in the series. Park Won-soon’s criticism of Japan’s colonial occupation of Korea, his advocacy of reconciliation between the two Koreas and his suit against the leadership of the fascist Shincheonji mind control cult (overlapped with the Unification Church), all bear on the political and economic dynamics of the Second World War, the Cold War, the Korean War, and the cartel arrangements that constitute a critical, though largely invisible, underpinning of the events of the Twentieth and Twenty-First centuries.
Essential to an understanding of these overlapping events is the landmark text Gold Warriors by Peggy and Sterling Seagrave. (FTR #‘s 427, 428, 446, 451, 501, 688, 689, 1106, 1107 & 1108 deal with the subject material of that consummately important book.)
Indeed, one cannot properly analyze the partition of Korea after World War II, the Korean War and the Cold War as separate events. They are interconnected and, in turn, are outgrowths of the complex politics of the Second World War and the actions and attitudes of Chiang Kai-shek’s narco-fascist dictatorship.
Although nominally a member of the Allied nations, Chiang’s Kuomintang government was primarily concerned with fending off Mao Tse-Tung’s communist armies and worked with the invading Japanese in critical areas. In particular, the Kuomintang’s profound involvement with the narcotics trade helped drive its trading with the Japanese.
The program begins with the obituary of general Paik Sun-yup of Korea, whose service in the Imperial Japanese Army during World War II has been a focal point of controversy in South Korea. General Sun-yup embodied the ongoing controversy in Korea over Japan’s occupation and the subsequent unfolding of events leading up to, and including the Korean War.
Again, the Japanese occupation of Korea was a major focal point of Park Won-soon’s criticism. “. . . . In 1941, he joined the army of Manchukuo, a puppet state that imperial Japan had established in Manchuria, and served in a unit known for hunting down Korean guerrillas fighting for independence . . .”
A little known factor in the development of the Korean partition and Cold War politics in Asia was the involvement of Chiang Kai-shek, his wife (the former Mei-Ling Soong, sister of Chiang’s finance minister T.V. Soong–the wealthiest man in the world at the time) and advisers in the Cairo Conference of 1943 and the subsequent Tehran Conference with Stalin and Churchill.
According to Colonel L. Fletcher Prouty, who flew the Kuomintang interests to Tehran from Cairo, Chiang and company were a driving force in setting the stage for war in Korea and Indochina.
While in Okinawa during Japan’s surrender in World War II, Colonel Prouty was witness to the early commitment of decisive military resources to the wars that were to take place in Korea and Indochina/Vietnam. ” . . . . I was on Okinawa at that time, and during some business in the harbor area I asked the harbormaster if all that new material was being returned to the States. His response was direct and surprising: ‘Hell, no! They ain’t never goin’ to see it again. One-half of this stuff, enough to equip and supply at least a hundred and fifty thousand men, is going to Korea, and the other half is going to Indochina.’ In 1945, none of us had any idea that the first battles of the Cold War were going to be fought by U.S. military units in those two regions beginning in 1950 and 1965–yet that is precisely what had been planned, and it is precisely what happened. Who made that decision back in 1943–45? . . . .”
To appreciate Chiang’s influence in the Cairo and Tehran conferences, it is important to understand that he was “working both sides of the street” in World War II.
American military supplies flown over the Hump and/or sent along the Burma Road at great risk and cost to Allied servicemen found their way into the hands of the Japanese, courtesy of KMT general Ku Chu-tung and his organized crime brother.
General Ku Chu-Tung commanded a devastating operation against the Chinese Communist New Fourth Army, illustrating why the Seagraves called him “one of the most hated men in China.”
Although obscured by the sands of time and propagandized history, Ku-Chu Tung’s actions illustrate why General Joseph Stilwell held Chiang Kai-Shek in contempt. Stillwell not only (correctly) viewed Chiang Kai-Shek as a fascist, but (correctly) saw him as an impediment to optimizing Chinese resistance to the hated Japanese invaders.
Collaborating with Kodama Yoshio, the Japanese crime boss and Admiral of the Imperial Japanese Navy, the Ku brothers swapped U.S. lend lease supplies for drugs.
It is important to note the role of the Black Dragon Society in the ascent of Kodama Yoshio. Black Dragon, along with Black Ocean, are key Japanese ultra-nationalist societies and the apparent forerunners of the Unification Church and, possibly the overlapping Shincheonji cult that was sued by Park Won-soon.
Kodama played a key role in the Unification Church, as discussed in FTR #‘s 291 and 970.
Acquiring key strategic raw materials for the Imperial Japanese Naval Air Force, Kodama bought many of these directly from the chief of Kuomintang secret service, General Tai Li, who was paid directly in heroin.
Before turning to the subject of the Korean War and its decisive influence on the disposition of global wealth and the resuscitation of the global cartel system, we recount the assassination of Kim Koo, an important Korean patriot, whose advocacy of reunification for Korea placed him in the crosshairs of American Cold War strategists. (Park Won-soon was called a “commie” for advocating reconciliation between the Koreas.) ” . . . . In June 1949, General Kim Chang-Yong, Rhee’s close advisor and Chief of Korea’s Counter-Intelligence Corps (CIC)—founded by and patterned after the CIA—conspired with American intelligence officers and a young lieutenant to assassinate Kim Koo. On June 26, 1949, while the seventy-three-year-old Kim was resting in his second-floor bedroom, Lieutenant Ahn Do hi walked past three policemen standing guard outside, entered the house, proceeded to Kim’s bedroom, and shot him to death. . . .”
On the eve of the outbreak of the Korean War, John Foster Dulles was in Seoul with Kodama Yoshio. It is not known just what they were doing, but Foster directly foreshadowed the impending (and allegedly unanticipated) North Korean invasion in a speech just before the commencement of hostilities.
Kodama recruited thousands of yakuza soldiers and Japanese World War II veterans to fight for South Korea, dressed in Korean uniforms.
Next, we highlight the 1951 “Peace” Treaty between the Allies and Japan, an agreement which falsely maintained that Japan had not stolen any wealth from the nations it occupied during World War II and that the (already) booming nation was bankrupt and would not be able to pay reparations to the slave laborers and “comfort women” it had pressed into service during the conflict.
Japan was not bankrupt at all when John Foster Dulles negotiated the Treaty. U.S. bombing left critical infrastructure intact, and the infusion of war loot helped boost the 1951 Japanese economy above its pre-World War II peak.
Foster Dulles’s role in the 1951 Peace Treaty with Japan, his curious presence in Seoul with Kodama Yoshio on the eve of the outbreak of the Korean War, his prescient foreshadowing of the conflict just before the North Korean invasion and the role of these events in shaping the post World War II global economic and political landscapes may well have been designed to help jumpstart the Japanese and German economies.
The Korean War did just that. ” . . . . A substantial infusion of money into this new Federal Republic economy resulted from the Korean War in 1950. The United States was not geared to supplying all its needs for armies in Korea, so the Pentagon placed huge orders in West Germany and in Japan; from that point on, both nations winged into an era of booming good times. . . .”
Indeed, John Foster Dulles’s world view enunciated a philosophy altogether consistent with those aims: ” . . . . He churned out magazine and newspaper articles asserting that the ‘dynamic’ countries of the world–Germany, Italy, and Japan–‘feel within themselves potentialities which are suppressed’ . . .”
Those economies, the cartels that dominated them and the Dulles brothers Cold War strategic outlook are dominant factors in the deep politics underlying the life, and death, of Park Won-soon.
As the title indicates, this program presents political and historical foundation for the exponential expansion of American biological warfare infrastructure following the 2001 anthrax attacks.
Important background information comes from the Whitney Webb article about DARPA spending on bat-borne coronaviruses.
The Broadcasting Board of Governors–a CIA “derivative”–and The Washington Times (owned by the Unification Church) helped develop disinformation about SARS CoV‑2 coming from a Chinese Biological Warfare lab. Both were instrumental in hyping the anthrax attacks as authored by Saddam Hussein, as well. The Washington Times also presented information floated by Steven Hatfill that foreshadowed subsequent charges that Saddam Hussein was developing bioweapons and was behind the 2001 anthrax attacks.
In addition, the Project For a New American Century was advancing an agenda in which genetically-engineered biological warfare technology as essential to continued American global dominance.
As will be seen below, a key functionary in the PNAC milieu was former Secretary of Defense Donald Rumsfeld, former chairman of the board of Gilead Sciences.
In FTR #‘s 1135, 1136 and 1137, we relied heavily on the Kris Newby’s Bitten: The Secret History of Lyme Disease and Biological Weapons. In that book, Ms. Newby networked with a group of experienced, Cold War biological warfare professionals whom she termed “the Brain Trust.” They were convinced that Fort Detrick scientist Bruce Ivins–the “lone nut” who conveniently committed suicide and was fingered as the sole perpetrator of the 2001 anthrax attacks–was framed. ” . . . . Among other subjects, they discussed . . . technical details on why they believed that their colleague Bruce Ivins had been framed as the anthrax mailer . . . .”
Much of the program centers on the 2001 attacks and the suspicion that focused on Steven Hatfill as a possible perpetrator of them. Although exonerated in the attacks, Hatfill was the focal point of considerable suspicion in connection with the event. Our suspicion is that he is an operative of one or another intelligence agency, CIA being the most probable.
We suspect that the anthrax attacks were a provocation aimed at justifying the invasion of Iraq and spurring development of the U.S. biological warfare capability.
Of particular note is the apparent “operational Teflon” worn by Hatfill. Although circumstantial evidence pointed in his direction, he appeared to be altogether “off limits” to investigative elements of Alphabet Soup. Don Foster noted the unusual treatment accorded to Hatfill by the powers that be.
Of significance, as well, are the numerous examples of foreshadowing of the forensic circumstances of the anthrax attacks, as well as other “false alarm” incidents that occurred before and after the fatal attacks. It requires little to see statements and articles by notables such as Bill Patrick and the seemingly ubiquitous Steven Hatfill as laying a foundation of credibility for subsequent events.
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.
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 Steven 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. . . .”
As noted in past programs, Gilead Sciences is very well-connected professionally, with former Secretary of Defense Donald Rumsfeld (among other political luminaries) serving on its board of directors. Rumsfeld was chairman of the board from 1997 until he left in 2001 to become George W. Bush’s Secretary of Defense.
Rumsfeld was Secretary of Defense during the period in which the 2001 anthrax attacks occurred.
During the post‑9/11 period of exploding government investments in biodefense programs, Secretary of Defense Donald Rumsfeld was still holding onto massive amounts of Gilead stock, which was increasing in value dramatically. What kind of relationship did Gilead develop with the US biodefense national security state during this period? That seems like a pretty important question at this point in time.
The U.S. government was among the customers whose purchases drove up the Gilead earnings and stock price: ” . . . . What’s more, the federal government is emerging as one of the world’s biggest customers for Tamiflu. In July, the Pentagon ordered $58 million worth of the treatment for U.S. troops around the world, and Congress is considering a multi-billion dollar purchase. . . .”
Several years into his tenure at the Pentagon, Rumsfeld made a killing on the sale of Gilead Sciences’ stock, which rose exponentially in value following its development of Tamiflu as a treatment for H5N1 avian flu.” . . . . The firm made a loss in 2003, the year before concern about bird flu started. Then revenues from Tamiflu almost quadrupled, to $44.6m, helping put the company well into the black. Sales almost quadrupled again, to $161.6m last year. During this time the share price trebled. Mr Rumsfeld sold some of his Gilead shares in 2004 reaping – according to the financial disclosure report he is required to make each year – capital gains of more than $5m. The report showed that he still had up to $25m-worth of shares at the end of 2004, and at least one analyst believes his stake has grown well beyond that figure, as the share price has soared. . . .”
Donald Rumsfeld was a signatory to the 1998 letter to President Clinton by the Project for a New American Century. That letter advocated a harder line against Iraq. ” . . . . Rumsfeld has strong ties to the Intelligence Community, as well as to the Atlantic Institute, and is a member of the Bilderberg group. He is a financial supporter for the Center for Security Policy. Rumsfeld was one of the signers of the January 26, 1998, Project for the New American Century (PNAC) letter sent to President William Jefferson Clinton. . . .”
DARPA and the Pentagon have into the application of genetic engineering in order to create ethno-specific biological warfare weapons, as discussed by the Project for a New American Century.
In past programs and posts, we have noted that DARPA was researching bat-borne coronaviruses. One can but wonder to what extent the PNAC doctrine helped spawn the DARPA research into coronaviruses and, possibly, the Covid-19 pandemic.
Continuing discussion about drug treatments for, and vaccines to prevent, Covid-19, this program sets forth information about the ongoing professional massaging of Gilead Sciences’ anti-viral remdesivir. Only modestly successful against SARS Cov‑2 (the virus that causes Covid-19), remdesivir has been propelled to the forefront of treatment regimens for the pandemic.
Of particular interest are the circumstances surrounding the CDC’s closure of the U.S. Army Medical Research Institute of Infectious Diseases. The USAMRIID–located at Ft. Detrick–had hosted Gilead Sciences’ animal trials of remdesivir. Remdesivir was developed to combat Ebola, and was a failure in its initial professional iteration.
In March of 2019, rhesus macaques were infected with Ebola at the USAMRIID as part of a project to allow remdesivir to be marketed as an Ebola treatment without meeting the professional standards of human testing. ” . . . This agreement was made possible through a 2018 Natural History Study (NHS) of Ebola virus conducted by USAMRIID in close collaboration with Gilead Sciences, Inc., the sponsor of remdesivir development . . .”
Many of the safety violations cited by the CDC in its critique of USAMRIID safety and security procedures concerned “non-human primates” infected with one or more “select agents” that were not named. The term “select agent” refers to a pathogen being used in laboratory procedures. Whether the “select agent” was Ebola, and whether the safety lapses were in connection with the remdesivir/rhesus monkey trials was not disclosed.
” . . . . Several of the laboratory violations the CDC noted in 2019 concerned ‘non-human primates’ infected with a ‘select agent’, the identity of which is unknown — it was redacted in all received documents, because disclosing the identity and location of the agent would endanger public health or safety, the agency says. In addition to Ebola, the lab works with other deadly agents like anthrax and smallpox. . . ..”
If, for the sake of argument, SARS-CoV‑2 research was indeed taking placing there was a very real risk of it escaping.
Remdesivir failed in its human trials as a treatment for Ebola: ” . . . . The antiviral drug remdesivir, made by Gilead, underperformed ZMapp. . . . Remdesivir and ZMapp have been dropped from the trial. . . .”
Following that dismal performance against Ebola, Gilead Sciences recast remdesivir as a broad spectrum antiviral, a marketing approach that has led to the drug being authorized to treat Covid-19.
In that professional reincarnation, it demonstrated altogether modest success in Covid-19 trials that were professionally criticized and which were badly skewed from a methodological standpoint.
After a tightening of professional methodological standards at the USAMRIID, it was disclosed that most of the institution’s operatives are private contractors! From the standpoint of institutional security, the broad use of private contractors renders USAMRIID subject to penetration by any number of potential miscreants. ” . . . . ‘A majority of our laboratory workers are contractors–putting teeth in the contracts to ensure they’re following the shalls, wills and musts are things we’ve done in the interim,’ said [Brigadier General Mike] Talley. . . .”
As noted in past programs, Gilead Sciences is very well-connected professionally, with former Secretary of Defense Donald Rumsfeld (among other political luminaries) serving on its board of directors. Rumsfeld was chairman of the board from 1997 until he left in 2001 to become George W. Bush’s Secretary of Defense. The firm’s stock has been heavily invested in by hedge funds, including Robert Mercer’s Renaissance Technologies. Gilead Sciences’ stock has been a major driver of the stock market’s performance.
Several years into his tenure at the Pentagon, Rumsfeld made a killing on the sale of Gilead Sciences’ stock, which rose exponentially in value following its development of Tamiflu as a treatment for H5N1 avian flu. ” . . . . The firm made a loss in 2003, the year before concern about bird flu started. Then revenues from Tamiflu almost quadrupled, to $44.6m, helping put the company well into the black. Sales almost quadrupled again, to $161.6m last year. During this time the share price trebled. Mr Rumsfeld sold some of his Gilead shares in 2004 reaping – according to the financial disclosure report he is required to make each year – capital gains of more than $5m. The report showed that he still had up to $25m-worth of shares at the end of 2004, and at least one analyst believes his stake has grown well beyond that figure, as the share price has soared. . . .”
The U.S. government was among the customers whose purchases drove up the Gilead earnings and stock price: ” . . . . What’s more, the federal government is emerging as one of the world’s biggest customers for Tamiflu. In July, the Pentagon ordered $58 million worth of the treatment for U.S. troops around the world, and Congress is considering a multi-billion dollar purchase. . . .”
(Recall that the H5N1 virus is one of the gain-of-function experiments that was suspended in 2014 and then greenlighted by the Trump administration in 2017. Those experiments engineered the virus to infect ferrets, a maneuver that made the virus communicable by upper respiratory activity. One can but wonder if those G‑O-F experiments were connected to the recasting of remdesivir as a broad spectrum antiviral.)
During the post‑9/11 period of exploding government investments in biodefense programs, Rumsfeld was still holding onto massive amounts of Gilead’s stock, which was rapidly increasing in value. What kind of relationship did Gilead develop with the US biodefense national security state during this period? That seems like an important question at this point in time.
In FTR #1136, we noted that the medical and scientific interests in charge of Lyme Disease treatment and diagnosis were not only financial beneficiaries of the therapeutic status quo, but were also tasked with discrediting Lyme patients and physicians who challenged that status quo. In light of the evidence that Lyme Disease was the outgrowth of biological warfare research, the professional relationship between governmental institutions involved with BW research and biotechnology and pharmaceutical firms profiting from the treatment of diseases those institutions develop and deploy is worth contemplating!
Previous broadcasts have documented the skewed, preferential treatment of remdesivir by powerful political and financial players with significant investment in the success of remdesivir.
The program concludes with three updates of previous lines of inquiry”
1.–Past programs have highlighted possible vectors into Wuhan for the SARS CoV‑2. We note that there was a workshop held at the Wuhan lab in early November of 2019, featuring scientists and bio-lab professionals from around the world. This conference may have been among the opportunities to spread the virus, and/or a co-vector and/or cross-vector. ” . . . . The workshop is designed for laboratory managers and directors, research and laboratory staffs mainly from developing countries who plan to carry out infectious disease research in biosafety facilities. The workshop will address key aspects of biosafety and provide practical training in high level biosafety laboratories (BSL). This workshop will invite a group of well-known scholars and experts from related fields at home and abroad to provide the theoretical and practical courses. . . .”
2.–As noted in past programs the Wuhan Institute of Virology was engaged in bat-borne coronavirus research, which included the genetic modification of such organisms. That research was a joint U.S./Chinese undertaking, with the U.S. funding coming from institutions which have fronted for American intelligence and the Pentagon. That joint U.S./Chinese undertaking was terminated by the Trump administration in May! In addition: ” . . . . Many of the scientists at the Wuhan Institute of Virology have been trained by the U.S. government’s PREDICT project. . . . USAID’s PREDICT project . . . will end this September after 10 years and two six-month extensions as USAID launches a new project that applies the data PREDICT collected. . . .”
3.–Other broadcasts have explored the Wuhan World Military Games–a military sports competition–as a possible vectoring vehicle. We update that path of inquiry with discussion of the U.S. delegation as a possible vectoring agent for the spread of the disease in the U.S. ” . . . . Contrary to the Pentagon’s insistence, however, an investigation of COVID-19 cases in the military from official and public source materials shows that a strong correlation exists in COVID-19 cases reported at U.S. military facilities that are home bases of members of the U.S. team that went to Wuhan. Before March 31, when the Pentagon restricted the release of information about COVID-19 cases at installations for security reasons, infections occurred at a minimum of 63 military facilities where team members returned after the Wuhan games. Additionally, the U.S. team used chartered flights to and from the games via Seattle-Tacoma International Airport. Washington was one of the earliest states to show a spike in COVID-19. . . .” We also note that the U.S. delegation contained: ” . . . . nine public-affairs officers . . . and two State Department personnel, according to DOD documents. . . .” “Public affairs officer” is a common cover for CIA personnel.
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. . . .”
This broadcast details the process of vetting the anti-Covid-19 drug remdesivir, highlighting the institutional shortcuts taken in testing the product, as well as the dubious nature of the billionaires networking with officials involved in the approval process.
Before analyzing remdesivir, however, we update discussion about the SARS CoV‑2 virus having been engineered, noting joint U.S.-Chinese projects in which bat-borne coronaviruses were genetically engineered. The processes used to modify the viruses would not show any overt evidence of human manipulation.
Most importantly, these projects received financing from institutions with documented links to U.S. intelligence and military interests.
Research into the history of GOF (gain-of-function) work on bat coronaviruses at the Wuhan Institute of Virology indicates multiple areas of U.S. intelligence presence in that work.
It was publicly disclosed in a 2017 paper that the US and China collaborated on “gain-of-function” research on bat coronaviruses to infect humans and that the work received funding from the United States Agency for International Development–a frequent cut-out for the CIA.
In addition, the work was also funded in part by the National Institutes of Health, which have collaborated with both CIA and the Pentagon in BSL‑4 (Bio-Safety-Level 4) projects.
The Wuhan Institute of Virology has also partnered with the USAMRIID since the mid-1980’s.
Important to note is the fact that it was public information that some of this work was done in a biosafety-level 2 laboratory, giving an observer intent on undertaking a biological warfare covert operation against China useful field intelligence about the vulnerability of WIV for such an “op.”
1.–The investigation of infectivity used undetectable methods, negating articles claiming the virus could not have been genetically engineered: ” Evidence has emerged that researchers at the Wuhan Institute of Virology (WIV) in China, working in collaboration with scientists in the USA, have been genetically engineering bat viruses for the past several years to investigate infectivity – using undetectable methods. . . . The evidence rebuts claims by journalists and some scientists that the SARS-CoV‑2 virus responsible for the current COVID-19 pandemic could not have been genetically engineered because it lacks the ‘signs’ or ‘signatures’ that supposedly would be left behind by genetic engineering techniques. . . .”
2.–Dr. Richard Ebright noted that the research was jointly funded by the U.S. and China, that Peter Daszak (about whom we have voiced reservations in the past) was one of the American collaborators. Furthermore, the research was funded in part by USAID, a common U.S. intelligence cut-out. ” . . . . Dr Richard Ebright, an infectious disease expert at Rutgers University (USA), has alerted the public to evidence that WIV and US-based researchers were genetically engineering bat viruses to investigate their ability to infect humans, using commonly used methods that leave no sign or signature of human manipulation. Ebright flagged up a scientific paper published in 2017 by WIV scientists, including Shi Zhengli, the virologist leading the research into bat coronaviruses, working in collaboration with Peter Daszak of the US-based EcoHealth Alliance. Funding was shared between Chinese and US institutions, the latter including the US National Institutes of Health and USAID. The researchers report having conducted virus infectivity experiments where genetic material is combined from different varieties of SARS-related coronaviruses to form novel ‘chimeric’ versions. This formed part of their research into what mutations were needed to allow certain bat coronaviruses to bind to the human ACE2 receptor – a key step in the human infectivity of SARS-CoV‑2. . . .”
3.–Furthermore, the researchers used a type of genetic engineering that leaves no signature of human manipulation: ” . . . . The WIV scientists did this, Ebright points out, ‘using ‘seamless ligation’ procedures that leave no signatures of human manipulation’. This is noteworthy because it is a type of genetic engineering that Andersen and his team excluded from their investigation into whether SARS-CoV‑2 could have been engineered – and it was in use at the very lab that is the prime suspect for a lab escape. . . .”
4.–In addition, Ebright highlights the 2015 work done by Ralph Baric in collaboration with WIV’s Shi Zhengli–a project we have discussed at length in the past: ” . . . . A group of scientists from the University of North Carolina in the USA, with the WIV’s Shi Zhengli as a collaborator, published a study in 2015 describing similar experiments involving chimeric coronaviruses, which were also created using standard undetectable genetic engineering techniques. . . .”
5.–Ebright also cites work done in a bio-safety level 2 laboratory. : ” . . . . Ebright points out that the paper states, ‘All work with the infectious virus was performed under biosafety level 2 conditions’. This level is suitable for work involving agents of only ‘moderate potential hazard to personnel and the environment’. . . .But they are not at fault in failing to use BSL‑4 for this work, as SARS coronaviruses are not aerosol-transmitted. The work does, however, fall under biosafety level 3, which is for work involving microbes that can cause serious and potentially lethal disease via inhalation. . . .”
6.–Dr. Jonathan Latham underscored the reservations expressed by many concerning “gain-of-function” experiments on these kinds of coronaviruses: ” . . . . The bioscientist Dr Jonathan Latham criticised the kind of research on bat coronaviruses that has been taking place in Wuhan and the USA as ‘providing an evolutionary opportunity’ for such viruses ‘to jump into humans’. Latham, who has a doctorate in virology, argues that this kind of work is simply ‘providing opportunities for contamination events and leakages from labs, which happen on a routine basis’. . . .”
U.S. Army Medical Research Institute of Infectious Disease–located at Ft. Detrick and closed by the CDC for safety violations in August, 2019.
Note, again, that the whole world was informed back in 2017 that dangerous research involving the creation of bat coronaviruses to infect humans was being carried out in China. Note again, that the research was funded in part by the US, including USAID–a frequent U.S. intelligence cut-out; the NIH–which has actively collaborated with both CIA and Pentagon. The WIV has also partnered with the USAMRIID.
Flash forward a couple of years and we have a nightmare virus that initially appeared to pop up nearby the WIV, with the Trump administration aggressively pushing the idea that it escaped from that lab.
In that context, we note the following:
1.–In 2017, China got approval for its first BSL‑4 lab in Wuhan, the first of several planned BSL‑4 labs. “A laboratory in Wuhan is on the cusp of being cleared to work with the world’s most dangerous pathogens. The move is part of a plan to build between five and seven biosafety level‑4 (BSL‑4) labs across the Chinese mainland by 2025, and has generated much excitement, as well as some concerns. . . . Some scientists outside China worry about pathogens escaping, and the addition of a biological dimension to geopolitical tensions between China and other nations. . . .”
2.–As will be seen below, the proliferation of BSL‑4 labs has sparked worries about “dual use” technology: ” . . . . The expansion of BSL-4-lab networks in the United States and Europe over the past 15 years — with more than a dozen now in operation or under construction in each region — also met with resistance, including questions about the need for so many facilities. . . .”
3.–The above-mentioned Richard Ebright notes that the proliferation of BSL‑4 labs will spur suspicion of “dual use” technology, in which ostensible medical research masks biological warfare research: ” . . . . But Ebright is not convinced of the need for more than one BSL‑4 lab in mainland China. He suspects that the expansion there is a reaction to the networks in the United States and Europe, which he says are also unwarranted. He adds that governments will assume that such excess capacity is for the potential development of bioweapons. ‘These facilities are inherently dual use,’ he says. . . .”
In the context of the above articles, 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 the U.S. and Europe have twelve BSL4 labs apiece, Taiwan has two, while 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. . . .”
Note, also that:
1.–The WIV has partnered with the U.S. Army’s Medical Research Institute of Infectious Diseases, located at Ft. Detrick.
2.–In early August of 2019, shortly before the recorded start of the outbreak in Wuhan, China, the U.S. Army Medical Research Institute of Infectious Diseases at that facility was closed down by the CDC due to multiple safety violations.“All research at a Fort Detrick laboratory that handles high-level disease-causing material, such as Ebola, is on hold indefinitely after the Centers for Disease Control and Prevention found the organization failed to meet biosafety standards. . . . The CDC sent a cease and desist order in July. After USAMRIID received the order from the CDC, its registration with the Federal Select Agent Program, which oversees disease-causing material use and possession, was suspended. That suspension effectively halted all biological select agents and toxin research at USAMRIID . . . .”
Following the update on the WIV and BSL‑4 laboratories, we pivot to analysis of the elevation of remdesivir as the “go-to” treatment du jour for Covid-19. Of paramount importance is the remarkable timeline: The DSMB (data safety and monitoring board) ” . . . . 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. . . . 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. . . .”
As will be seen, it was on 4/29 that Joe Grogan resigned. (See below.)
When positive news on a NIAID study on the drug remdesivir were released–on 4/29–it drove broad gains in the stock market. In FTR #1131, we noted that disclosures concerning positive news about Moderna’s experimental Covid-19 vaccine also proved to be a similar driver of the stock market, as well as of Moderna’s stock.
Discussion of the hard details of several remdesivir trials begins with discussion of an NIAID trial that helped move the markets, as seen above. The trial was a modest success, indicating that recovery for recently infected patients was about 31% faster than for placebo. There was no significant statistical difference in mortality–the most important measure of effectiveness according to many experts.
” . . . . During an appearance alongside President Trump in the Oval Office, Anthony Fauci, the director of NIAID, part of the National Institutes of Health, said the data are a ‘very important proof of concept’ and that there was reason for optimism. He cautioned the data were not a ‘knockout.’ At the same time, the study achieved its primary goal, which was to improve the time to recovery, which was reduced by four days for patients on remdesivir. The preliminary data showed that the time to recovery was 11 days on remdesivir compared to 15 days for placebo, a 31% decrease. The mortality rate for the remdesivir group was 8%, compared to 11.6% for the placebo group; that mortality difference was not statistically significant. . . .”
Next 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. . . .”
6.–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. . . .”
7.–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.’ . . . .”
Next, we analyze a STAT News excerpt that goes into more of the concerns about the Gilead study design.
The Gilead study was designed without any control group, so the question of how much remdesivir actually helps sick patients (or doesn’t help) can’t be definitively answered by that study.
The article also gives Gilead’s explanation for why they left out a control group: due to the limited supplies of the drug the company decided to prioritize on producing more of the drug itself rather than a placebo control. It’s an explanation that only makes sense if producing placebo doses was somehow a significant technical challenge, which seems dubious.
Due to a lack of a control group, the study instead focuses on answering the question of whether or not the recovery times for patients differs between groups receiving a 10-day course of the drug vs a 5‑day course. The patients were severely ill but not on ventilators when enrolled in the study (so the patients that need the drug most weren’t tested). The preliminary results released Wednesday suggest there is no difference between the recovery times for the two groups.
1.–The Gilead study lacked a control group: ” . . . . But outside experts in clinical trial design worry that the results, instead of leading to a clear picture of whether the medicine is effective, will instead muddy the waters further. The main concern, they say, stems from the fact that the Gilead trial expected to read out this week, which was conducted among patients with severe disease, lacks a control group — that is, patients who are randomly assigned to receive the best treatment available, but not remdesivir. As designed, the only randomization is the duration of treatment: either five days or 10 days of drug. Without a true control group of patients, many experts say, it will be difficult to determine whether remdesivir is effective. . . .”
2.–The above-mentioned Steven Nissen summed up the usefulness of the Gilead trial. ” . . . . ‘The overall study itself has little or no scientific value since all patients are receiving the drug,’ said Steven Nissen, the chief academic officer at the Cleveland Clinic and lead investigator of many trials for heart drugs that have been approved by the Food and Drug Administration. ‘The study, as designed, is essentially useless and cannot be used by the FDA for consideration of remdesivir for approval to treat coronavirus,’ Nissen said. . . .”
3.–Gilead’s spokesperson alleged that the company had a limited supply of placebo and remdesivir. ” . . . . ‘In the early stages of the pandemic, we not only had a limited supply of remdesivir but also a limited supply of the matched placebo required for placebo-controlled studies,’ said Amy Flood, a Gilead spokesperson. ‘We chose to prioritize manufacturing active drug over placebo, and we provided our supply of placebo to China and NIAID for their studies of remdesivir.’ . . .”
5.–A number of critics shared Steven Nissen’s opinion about the scientific value of the study. ” . . . . Critics point to Gilead’s decision to compare two groups given remdesivir for either five days or 10 days. The problem with this strategy, they say, is that an ineffective drug that did nothing and a very effective drug that consistently helped patients overcome the virus would look the same in such a study. Only if the 10-day course were more effective, or if it was worse because of side effects, would the study have any clear result. . . .”
6.–Nissen was more optimistic about a second forthcoming Gilead trial. Sloan Kettering’s Peter Bach did not share that optimism. ” . . . .Yet another trial in less sick patients, also run by Gilead, does have a control group and may give a clearer answer. Nissen sees ‘a reasonable study design.’ But Bach was more critical, saying that even though that study has a control group, the lack of a placebo means the study might not be trustworthy. That’s because its main goal, time to improvement of symptoms, could be affected by the perceptions of clinicians and the patients themselves. Bach said the hospitals conducting the study ‘are easily capable of wrapping syringes in brown paper and blinding the whole thing. I don’t understand why you would run a trial like this.’ . . . .”
Although it was cut short due to the waning of the pandemic in China, a WHO-leaked study was not encouraging with regard to remdesivir’s efficacy as a treatment for Covid-19.
1.–The Chinese study was a ramdomized controlled trial: ” . . . . Encouraging data from patients in that study at the University of Chicago were described by researchers at a virtual town hall and obtained by STAT last week. However, unlike those data, these new results are from a randomized controlled trial, the medical gold standard. . . .”
2.–The Chinese study found that remdesivir was of no value in preventing Covid-19 deaths. As noted above, the effect of the drug on mortality was the main consideration. Our society has not been shut down to afford people shorter stays in the hospital, but to prevent death. ” . . . . According to the summary of the China study, remdesivir was ‘not associated with a difference in time to clinical improvement’ compared to a standard of care control. After one month, it appeared 13.9% of the remdesivir patients had died compared to 12.8% of patients in the control arm. The difference was not statistically significant. . . .”
3.–The Chinese study produced a grim assessment of remdesivir: ” . . . . ‘In this study of hospitalized adult patients with severe COVID-19 that was terminated prematurely, remdesivir was not associated with clinical or virological benefits,’ the summary states. The study was terminated prematurely because it was difficult to enroll patients in China, where the number of Covid-19 cases was decreasing. An outside researcher said that the results mean that any benefit from remdesivir is likely to be small. ‘If there is no benefit to remdesivir in a study this size, this suggests that the overall benefit of remdesivir in this population with advanced infection is likely to be small in the larger Gilead trial,’ said Andrew Hill, senior visiting research fellow at Liverpool University. . . .”
After discussing a number of problems that Gilead Sciences may encounter in the production of significant quantities of remdesivir to be effective, the broadcast concludes with discussion of the inappropriately-named “Scientists to Stop Covid-19.”
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 Peter Thiel and 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 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.
1.–” . . . . 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 with a piece about 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 imfluence of “Scientists to Stop Covid-19.”
In past posts and programs, we have noted that Moderna–which has been selected to develop a Covid-19 vaccine–has been substantially underwritten by the Pentagon (DARPA). The vaccine they are developing is a mRNA (messenger RNA) vaccine–a type of vaccine that has never been administered to human subjects and is seen as very risky: ” . . . . Both DNA and mRNA vaccines involve the introduction of foreign and engineered genetic material into a person’s cells and past studies have found that such vaccines ‘possess significant unpredictability and a number of inherent harmful potential hazards’ and that ‘there is inadequate knowledge to define either the probability of unintended events or the consequences of genetic modifications.’ . . .” The head of Trump’s “Operation Warp Speed” coronavirus vaccine program is Moncef Slaoui, formerly in charge of Moderna’s product development committee. He says that he had ” . . . .‘recently seen early data from a clinical trial with a coronavirus vaccine, and these data made me feel even more confident that we will be able to deliver a few hundred million doses of vaccine’ — enough to inoculate much of the United States — ‘by the end of 2020. . . .” This despite the fact that no vaccine has been approved for human use in less than four years. Slaoui will be assisted by General Gustave F. Perna, whose appointment was facilitated by General Mark A. Milley, Chairman of the Joint Chiefs. Interestingly, Slaoui holds more than $10 million worth of Moderna stock, which has increased 184% since the beginning of the year, due to ” . . . . more than $400 million from the federal government to assist trials of a coronavirus vaccine. . . .”
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