Tag: human experimentation

Researchers Push AI DESIGNED ‘Super Vaccine’

Cambridge scientists are hailing an AI-crafted “super-antigen” as a breakthrough that could ‘get ahead of pandemics’, blanket-protect against every COVID variant, and spare the world future lockdowns while saving millions of lives.

Yet the same public that lived through the last round of experimental shots is not buying the hype. Responses to the announcements have been blunt, laced with references to documented harms, AI’s well-known limitations, and fresh warnings from cancer specialists who watched stable patients relapse after previous boosters.

University of Cambridge researchers, led by Professor Jonathan Heeney, say they have produced the first antigen designed entirely by artificial intelligence and tested in humans.

The team fed AI systems genetic sequences from multiple coronaviruses collected through ongoing surveillance programs. The algorithm then assembled a “super-antigen” intended to train the immune system to recognize whole virus families rather than single strains that keep mutating.

Early human testing involved 39 volunteers and produced what researchers called modest immune responses but no major safety red flags in the initial readout. A larger study with roughly 200 participants is now running to measure stronger and more durable protection.

The same platform is being extended toward universal flu shots, H5N1 bird flu candidates, and vaccines against viral hemorrhagic fevers.

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Lyme Vaccine Clinical Trials: History Repeating?

Why is there so much controversy surrounding Lyme disease? Why does it seem you can’t get an accurate Lyme disease test?

The State of Lyme

The incidence of Lyme disease is approaching half a million cases per year in the United States, according to a 2021 Centers for Disease Control & Prevention (CDC) report based on data from commercial insurance claims. Yet fewer than 40,000 cases are reported to the CDC in any given year, exposing a massive discrepancy between the actual prevalence of the disease and the few cases that meet the CDC’s surveillance reporting definition.

Despite its alarming incidence rate and often catastrophic effects on human health, there has been little advancement in diagnostic and therapeutic technologies for Lyme in the last 40 years. The CDC and Infectious Diseases Society of America (IDSA) continually support only the use of outdated serological techniques that are known to be inadequate, while simultaneously acknowledging that better tests are needed. The reasons for such double-speak and neglect are inextricably intertwined with the sordid history of Lyme disease vaccines.

Lyme vaccine development has continued for the last three decades despite evidence that the causative organism—the spirochetal bacteria Borrelia burgdorferi—evades immunity in multiple ways that may make it impossible for a vaccine to prevent infection. The most recent effort, a candidate known as VLA-15 from Pfizer and French biotech Valneva, is now in phase III trials. Last February it was revealed that due to alleged violations of good clinical practice, Pfizer had shut down all trial sites run by contractor Care Access, eliminating roughly half of the enrolled participants.

Pfizer’s record of “engaging in illegal and corrupt marketing practices, bribing physicians and suppressing adverse trial results” may alone warrant suspicion about their recent actions. But in the context of a Lyme vaccine, suspicion should be heightened. The last Lyme vaccine on the market, SmithKline Beecham’s LYMErix, was withdrawn in 2002 amid numerous injury claims, federal agency hearings, and class action lawsuits. Which begs the question, is history repeating?

Stepping back three decades

In June 1994, the U.S. Food and Drug Administration’s (FDA) Vaccines and Related Biological Products Advisory Committee (VRBPAC) devoted a lengthy meeting to the three companies that had Lyme vaccines in development. According to the official meeting transcript, the primary order of business was to answer the question, “Is the CDC case definition for Lyme disease appropriate for a pivotal efficacy trial?”

Why would this even be a question? The standard diagnostics at the time—mainly the ELISA, a serologic assay that measures antibodies produced against the bacteria—were known to produce a large proportion of false negatives. When the CDC discontinued routine testing of samples in its labs in 1988, it stated in a letter to the Oregon Public Health Laboratory that the sensitivity of the ELISA ranged from 13% to 27% in clinically recognized cases. Obviously, this would hamper any trial operator’s ability to assess possible Lyme infection and the vaccine’s overall effectiveness. If you can’t diagnose cases, how can you determine whether your vaccine works?

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Secret Trial of Pfizer RSV Vaccine Killed Two Infants in the 1960s — Their Families Just Sued the U.S. Government

The families of two Black infants who died during a 1960s experimental RSV vaccine trial have filed a federal lawsuit against the U.S., alleging government researchers enrolled the babies in a dangerous medical experiment without their parents’ knowledge or consent, The New York Times reported.

The lawsuit, filed May 22 in the U.S. District Court for the District of Columbia, alleges the National Institutes of Health (NIH) and other researchers, in 1965 and 1966, subjected dozens of infants — most or all of them from low-income Black families — to testing of Pfizer’s Lot 100 experimental vaccine for respiratory syncytial virus, or RSV.

Two infants, Victor Marcellus King and Ross Otto Hambrick, later died after developing vaccine-associated enhanced respiratory disease (VAERD), a severe respiratory illness caused by the vaccine.

VAERD occurs when a vaccinated child who never had RSV is exposed to the virus and develops a more severe case of RSV than they would have if they hadn’t received the vaccine.

The suit was filed by Sharlette Hambrick and Darius King, acting as representatives of the estates of their deceased brothers. They allege federal researchers failed to obtain informed consent from the children’s parents, withheld critical information about prior vaccine failures, and continued the study despite mounting evidence that the vaccine was causing severe reactions in participants.

The complaint also alleges that the tissue samples from the babies who died were later used to develop the RSV vaccines and monoclonal antibody shots that have been approved in the last several years — providing a financial boon for drugmakers.

“Medical research in the United States has a long, troubled racial history,” the complaint states, comparing the alleged conduct to other notorious examples of unethical experimentation involving Black Americans, including the Tuskegee Syphilis Study and the exploitation of Henrietta Lacks.

The infants’ families were unaware the babies had been subjected to the experiment until a reporter from Undark magazine contacted them while investigating the story in 2023.

The reporter found the babies’ names in a doctor’s government-issued laboratory notebook and other paperwork from the clinical trial, the Times reported.

Parents not told infants were being enrolled in trial for experimental vaccine

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The Bizarre Soviet Experiments That Attempted To Understand Psychic Powers

Could someone stop a heart with their mind? Could objects move through the use of mental imagery? Could someone communicate from the shore with a submarine through their thoughts? These were the premises of several strange experiments performed under direction of the Soviet Union. Citizens believed to possess unique parapsychological abilities were tested and studied by renowned scientists in an effort to illuminate the supposed physics that were thought to underlie supernatural abilities. Whether “bioplasma” or “psi particles,” brilliant minds were determined to reveal the science behind the paranormal.

The Cold War was a time rife with competition between the United States and the Soviet Union. The nations battled for control of territories left vulnerable in the aftermath of World War II and fought to claim ideological supremacy. Fear and paranoia were stoked in the American public by the declaration of an arms race, although it was later revealed that the Soviet Union did not have access to such destructive weapons as the U.S. had claimed.

Both governments also competed in the realm of scientific advancement, most famously characterized by the Space Race, in which the U.S. managed to land people on the moon. In a time of such fierce competition, it was all hands on deck, including some scientists with rather peculiar beliefs. The U.S. received intelligence that the Soviet Union was attempting to capture the paranormal using the tenets of the scientific method, gaining an upper hand through telekinesis, telepathy, and clairvoyance.

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Rep. Anna Paulina Luna Fires off Preservation Letter to CIA After Whistleblower Testifies that CIA Seized MKUltra and JFK Assassination Files from Tulsi Gabbard 

Rep. Anna Paulina Luna (R-FL) and the House Oversight Committee issued a warning and subpoena to the CIA and Director John Ratcliffe on Wednesday. The action came after a whistleblower accused the agency of seizing documents related to the JFK assassination and MKUltra — the CIA’s experimentation on human behavior and mind control through the use of drugs — from the Office of the Director of National Intelligence, Tulsi Gabbard.

CIA whistleblower James Erdman III testified during a Senate Homeland Security Committee hearing earlier that the CIA “took back 40 boxes of JFK files and MKUltra files being processed for declassification by DNI Gabbard” in what he described as “documented efforts to circumvent oversight.”

During an interview with News Nation’s Katie Pavlich following the bombshell testimony, Luna sounded the alarm on the CIA’s alleged refusal to follow President Trump’s executive orders and its aversion to transparency.

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CIA Went Rogue, Raided Tulsi’s Office to Seize Papers

A breaking news alert from Fox News, apparently confirmed by a Republican congresswoman, states that the Central Intelligence Agency went rogue, raiding the office of the Director of National Intelligence (DNI) to seize files.

It seems from the Fox News report that the CIA seized the files just now, though a whistleblower from the agency who testified to Congress today referred to the wrongful seizure of files in his testimony. It is therefore not clear if the raid occurred today or before the testimony, or if there was more than one seizure. In either case, Rep. Anna Paulina Luna is giving the CIA 24 hours to return the files in question or face consequences.

The CIA was allegedly after the files on the assassination of President John F. Kennedy and the MK-Ultra human experimentation scandal. The story on the raid is developing but seems to be legitimate, and illustrates the need for drastic cuts in our Deep State. Donald Trump cannot hope to prevent such egregious acts by merely replacing top leadership. The majority of employees at the CIA and FBI worked there during the Biden-era weaponization of justice and believe they are not accountable to Trump or We the People.

DNI Tulsi Gabbard was reportedly in the process of declassifying the JFK and MK-ULTRA files, and it seems the CIA gave us indirect confirmation that there is something in those files that they desperately do not want anyone to know. The problem is that we don’t know if they will be able to destroy the files or not before the Trump administration can get them back. If the raid just occurred and did not happen previously in the last couple of days, it is interesting to note that President Trump was out of the country in China, and therefore unable to be present personally to deal with the situation. Hopefully, Vice President Vance is on the job.

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CIA Ran MK-ULTRA Experiments on Prisoners of War in U.S. Custody, Declassified Docs Confirm

Korean prisoners of war in the 1950s were subjected to early MK-ULTRA experiments while in American custody, according to recently declassified CIA documents which confirm these experiments for the first time.

The only reporting that previously referenced Koreans being used as guinea pigs for these experiments was journalist John Marks’s landmark 1979 book, The Search for the “Manchurian Candidate.” Using CIA documents, Marks traced the now-infamous MK-ULTRA project to its start, when it was known as Project Bluebird. In the book, Marks describes how, in October 1950, 25 unnamed North Korean POWs were chosen as the first test subjects to receive “advanced” interrogation techniques, with the overt goal of “controlling an individual to the point where he will do our bidding against his will and even against such fundamental laws of nature as self-preservation.”

While MK-ULTRA is best known for its invasive experimentation — like LSD dosing and torture — the documents confirm Korean POWs were the unwitting subjects of less splashy attempts at mind control, like being subjected to polygraph tests, with plans for other invasive testing.

The declassified documents, which the National Security Archive released between December 2024 and April 2025, are available through a special collection titled “CIA and the Behavioral Sciences: Mind Control, Drug Experiments and MK-ULTRA.” The National Security Archive website states that the collection “brings together more than 1,200 essential records on one of the most infamous and abusive programs in CIA history.”

The first reference to “Project Bluebird” in the NSA’s collection is an office memorandum from April 5, 1950. Addressed to CIA Director Roscoe H. Hillenkoetter, the document lays out the project’s goals, required training, and budget, all while emphasizing that knowledge of Project Bluebird “should be restricted to the absolute minimum number of persons.”

The memo includes detailed plans for interrogation teams trained to utilize the polygraph, various drugs, and hypnotism “for personality control purposes.” These teams were to be made up of three people: a doctor (ideally a psychiatrist), a hypnotist, and a polygraph technician. The memo clarifies that while the doctor and technician would need to undergo approximately five months of training, the Inspection and Security Staff’s own department hypnotist could be made available immediately. In a later memo from February 2, 1951, there are inquiries into acquiring six “hypospray” devices: experimental instruments designed to covertly inject sedatives through the skin via “jet injection.” There’s a request to investigate modification of a “tear gas pencil” and other “devices of unestablished action,” such as the “German ‘Scheintot’ [sic] (appearance of death) pistol.”

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Big Pharma Giants Pfizer and BioNTech Forced to Shut Down COVID-19 Booster Shot Trials After Americans Refuse to Be Guinea Pigs

Major Big Pharma companies have abruptly halted their latest COVID-19 mRNA “booster” trial because they literally couldn’t find enough willing participants.

After years of gaslighting the American public, raking in hundreds of billions in profits from experimental shots that were shoved down our throats under the guise of “public health,” the same corporations that partnered with the Biden regime, Anthony Fauci, and the lying mainstream media are now facing the cold, hard reality: Americans are done being lab rats.

According to internal letters sent to trial investigators and obtained by Reuters, Pfizer is ending its study of “updated” shots in healthy adults aged 50 to 64.

The company admitted it was “unable to generate relevant data” because recruitment had effectively hit a brick wall.

Reports indicate that more than 80% of potential recruits didn’t even make it past pre-screening, or simply refused to participate.

The trial, which aimed to enroll a massive 25,000 to 30,000 participants, folded after failing to meet even the most basic enrollment targets.

This comes at a time when the “science” is being scrutinized like never before. Under the current administration, the FDA has been pressured to actually require randomized placebo-controlled trials, the very thing skeptics have been demanding for years.

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CIA accused of secret bioweapon experiments linked to major outbreak in its own people

A biochemist has claimed to have found evidence that the modern Lyme outbreak in the US could have been the result of CIA bioweapon experiments.

Dr Robert Malone, who helped lay the groundwork for mRNA vaccine technology, made the explosive allegations this week after analyzing declassified government documents, historical records from Cold War biological weapons programs and scientific research on tick-borne diseases.

Malone highlighted experiments in the 1960s that allegedly released more than 282,000 radioactive ticks in Virginia and open-air tick research at Plum Island, a federal laboratory located near the Connecticut community where Lyme disease was first identified.

The experiments were designed to track how disease-carrying ticks spread through the environment, with scientists marking the parasites using radioactive Carbon-14 so their movements could be detected with Geiger counters, a portable, gas-filled instrument. 

Malone’s report argued the research was part of a much larger Cold War biological weapons program known as Project 112, which involved dozens of secret tests aimed at studying how insects could be used to spread pathogens.

The program, authorized by Defense Secretary Robert McNamara in 1962, oversaw 134 planned tests and included facilities capable of breeding millions of infected insects each week.

According to the report, the same region where these experiments took place later experienced an unprecedented surge in tick-borne illnesses.

Malone’s claims follow calls from US officials to investigate whether federal agencies experimented with pathogen-laden ticks as tools of war.

In December 2025, an amendment by New Jersey Representative Chris Smith called for a review of military, NIH and USDA projects from 1945 to 1972 involving Spirochaetales and Rickettsiales, bacteria linked to tick-borne diseases. 

Health and Human Services Secretary Robert F Kennedy Jr has also suggested Lyme disease may have originated from a failed US bioweapons program in the 1970s tied to research at Plum Island. 

Plum Island is an 840-acre island off the northeastern coast of Long Island, New York, and home to the Plum Island Animal Disease Center, a government lab used since the 1950s to study infectious animal diseases.

However, the Department of Homeland Security has repeatedly said Lyme disease was never studied at the facility.

Malone’s report also claims key research into a second tick-borne pathogen may have been suppressed.

He alleged the government sidelined research on a pathogen known as the ‘Swiss Agent,’ which was detected in Lyme patients in Europe during the 1970s.

Malone, an expert in biology who earned multiple degrees at the University of California, also accused the government of suppressing research on a second disease called the ‘Swiss Agent’ found in Lyme patients in Europe in the 1970s.

Unpublished papers from Willy Burgdorfer, the scientist who discovered the bacterium that causes Lyme disease, suggested the pathogen complicated treatment because it triggered persistent symptoms that did not respond to standard antibiotics. 

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UK’s approval of self-amplifying vaccines is a catastrophic “mistake”

In 2018, Imperial College London entered into a partnership with the Coalition for Epidemic Preparedness Innovations (“CEPI”) to develop a self-amplifying RNA vaccine platform (“saRNA”) to enable tailored vaccine production against multiple viral pathogens.

“The consortium aims to develop ‘RapidVac’, a synthetic saRNA vaccine platform, which will be used to produce vaccines against influenza, rabies and Marburg, with hopes to move these products to Phase I clinical testing in humans,” Pharma Times wrote.

In June 2020, a team at Imperial College London announced that it had developed a vaccine against covid that used “bits of genetic code (called self-amplifying RNA).” 

“Once inside the cell, the self-amplifying RNA produces copies of itself, which can instruct the cell’s own machinery to make the coronavirus protein,” Imperial College said.  “The muscle cells will then produce lots of the spike protein … Some of the proteins will be presented on the surface of the muscle cells … When the immune system comes across these tiny spikes, it recognises them as foreign.”

Imperial College completed Phase I and II clinical trials, but due to the approval and rollout of several other covid injections, the decision was made not to proceed with trials in the UK.  Instead, the team focused their UK efforts on “developing self-amplifying RNA technology to adapt to new variants, to boost other vaccines and to be deployed against future pandemic threats,” Imperial College threatened in a January 2021 article.

Imperial College has also been working on saRNA vaccines for rabies, Chikungunya, Ebola, Lassa and Marburg. It has been a key pioneer in saRNA vaccine research, particularly through its collaborations with VaxEquity and AstraZeneca, but it is the US company Arcturus Therapeutics’ saRNA vaccine that has been approved for use in the UK.

On 2 January 2026, the Medicines and Healthcare products Regulatory Agency (“MHRA”) approved Kostaive (also known as Zapomeran), a self-amplifying mRNA (“sa-mRNA”) covid vaccine developed by Arcturus Therapeutics, for use in adults aged 18 years and older. 

Kostaive uses sa-mRNA technology, which includes genetic instructions for both the SARS-CoV-2 spike protein and a viral replicase enzyme, enabling the mRNA to amplify itself within cells.  The stated aim is to enhance immune response with lower doses.

As Pharma Phorum described it, “Unlike regular mRNA vaccines, sa-mRNA vaccines – as their name suggests – instruct the body to make more mRNA and protein to boost the immune response, rather than relying on a finite dose which results in protection waning over time.”

“It is administered as a single 0.5 ml booster dose by intramuscular injection into the upper arm … Once injected, the sa-mRNA in lipid nanoparticles enters cells, where it directs production of the spike protein. The immune system recognises this protein as foreign,” Pharmacally wrote.

Recognising a protein in our bodies as foreign is the problem.  As Dr. Mike Yeadon explained in a video last month, making our bodies’ cells manufacture a foreign protein that our immune systems would attack results in autoimmune conditions, a self-to-self attack where our immune systems attack our own cells, thinking they are foreign invaders that need to be killed.

It would seem the vaccine industry is not satisfied with the effectiveness of mRNA vaccines waning over time, what they might refer to as “waning protection,” and so are seeking to extend the risk of autoimmune conditions through the use of saRNA “vaccines.”

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