The UK government and Wellcome Trust and the Bill and Melinda Gates Foundation (BMGF) jointly financed the Recovery Trial.64 The principal investigator (PI), Peter Horby, is a member of SAGE and is the chairman of NERVTAG, the New and Emerging Respiratory Virus Threats Advisory Group, both important committees that give the UK government advice on mitigating the pandemic.65,66 Horby’s willingness to risk death of patients given toxic doses of HCQ fueled his subsequent rise in the UK medical hierarchy. Horby received a parade of extraordinary promotions after he orchestrated the mass poisonings of senior citizens. Queen Elizabeth recently knighted him.67
Gates’s fingerprints are all over this sanguinary project. Despite suspiciously missing pages, the published minutes of WHO’s part-secret March and April meetings show these medical alchemists establishing the lethal dosing of chloroquines (CQ and HCQ) for WHO’s Solidarity clinical trial. Only four participants attended the second WHO meeting to determine the dose of HCQ and CQ for the Solidarity trial. One was Scott Miller, the BMGF’s Senior Program Officer. The report admits that the Solidarity trial was using the highest dose of any recent trial.68
The report acknowledges that, “The BMGF developed a model of chloroquine penetration into tissues for malaria.”69 BMGF’s unique dosing model for the studies deliberately overestimated the amount of HCQ that necessary to achieve adequate lung tissue concentrations. The WHO report confesses that, “This model is however not validated.” Gates’s deadly deception allowed FDA to wrongly declare that HCQ would be ineffective at safe levels.
The minutes of that March 13, 2020 meeting suggest that BMGF knew the proper drug dosing and the need for early administration. Yet their same researchers then participated in deliberately providing a potentially lethal dose, failing to dose by weight, missing the early window during which treatment was known to be effective, and giving the drug to subjects who were already critically ill with comorbidities that made it more likely they would not tolerate the high dose. The Solidarity trial design also departed from standard protocols by collecting no safety data: only whether the patient died, or how many days they were hospitalized. Researchers collected no information on in-hospital complications. This strategy shielded the WHO from gathering information that could pin adverse reactions on the dose.
The report of WHO’s HCQ trial notes that WHO researchers did not retain any consent forms from the elderly patients they were overdosing, as the law in most countries requires, and makes the bewildering claim that some patients signed consent forms “in retrospect”—a stunning procedure that is unethical on its face. The WHO’s researchers noted in their interim report on the trial, “Consent forms were signed and retained by the patients; [An extremely unorthodox and suspicious procedure that suggests that there may have been no formal consents] but noted for record that, consent was generally prospective, but could (where locally approved) be retrospective.” One wonders if researchers notified their families of the high dose they were giving to their elderly parents and grandparents in locked COVID wards to which they denied family members access.
The researchers evinced their guilty knowledge by concealing the research records of the doses they used in Solidarity when they filed their trial reports. They also omitted dosing numbers from the report of WHO’s meeting to determine the dose, and omitted details of dosing from the WHO’s Solidarity trial registration.
Another group of researchers using overdose concentrations of chloroquine published their study as a preprint in mid-April 2020 (and quickly brought to print) in the preeminent journal, JAMA (The Journal of the American Medical Association) In this murder-for-hire scheme, Brazilian researchers used a dose of 1,200 mg/day for up to ten days of CQ.70 According to a 2020 review of CQ and HCQ toxicity, “As little as 2–3 g of chloroquine may be fatal in adult patients, though the most commonly reported lethal dose in adults is 3–4 g.” Predictably, so many subjects died in the Brazilian high dose study (39 percent, 16 of 41 of the subjects who took this dose) that the researchers had to halt the study. The subjects’ mean age was only 55.71 Their medical records revealed EKG changes characteristic of CQ toxicity.
The WHO and UK trial coordinators must have known this information, but they made no efforts to stop their own overdose trials, nor to lower the doses.
Although Gates did not fund the JAMA study directly (it’s very possible he funded it indirectly through a nebulous list of funders), the senior and last author, Marcus Vinícius Guimar?es Lacerda, has been a Gates-funded researcher on numerous projects. Further, the BMGF has funded multiple projects at the same medical foundation where he and the first, or “lead” author, Borba, work in Manaus, Brazil.72 (Traditionally, the first listed author is generally seen as the senior and accountable author.)
Gates and his cabal used an arsenal of other deceptive gimmickry to assure that HCQ would appear not just deadly, but ineffective. Each of the studies that Gates funded failed to incorporate Zithromax and zinc—important components of HCQ protocols. All of the Fauci, Gates, WHO, Solidarity, Recovery and Remap-COVID studies administered HCQ at late stages of COVID infection, in contravention of the prevailing recommendations that deem HCQ effective only when doctors administer it early.73,74 Viewing this orchestrated sabotage with frustration, critics accused the Gates grantees of purposefully designing these studies, at best, to fail and, at worst, to murder.75 Brazilian prosecutors have accused the authors of the study of committing homicide by purposefully poisoning the elderly subjects in their study with high doses of chloroquine.76
All through 2020, Bill Gates and Fauci lashed out against HCQ every chance they got. During the early stages of the pandemic in March, Bill Gates penned an op-ed in The Washington Post.77 Besides calling for a complete lockdown in every state, along with accelerated testing and vaccine development, Gates warned that: “Leaders can help by not stoking rumors or panic buying. Long before the drug hydroxychloroquine was approved as an emergency treatment for COVID-19, people started hoarding it, making it hard for lupus patients who need it to survive.”78
This, of course, was a lie. The only ones hoarding HCQ were Dr. Fauci and Rick Bright, who had padlocked 63 million doses in the Strategic National Stockpile79—more than enough to supply virtually every gerontology-ward patient in America. Despite such efforts to create a shortage, none existed. HCQ is cheap, quick, and easy to manufacture, and since its patent is expired, dozens of manufacturers around the world can quickly ramp up production to meet escalating demand.