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(LifeSiteNews) – mRNA technology pioneer Dr. Robert Malone participated Thursday in the White Coat Summit hosted by America’s Frontline Doctors, during which he laid out information and analysis concerning the “good, the bad, and the ugly” of genetic vaccine technology.

Malone, a prominent critic of the government and medical establishment’s response to the COVID-19 outbreak, summarized the rollout of the mRNA-based COVID vaccines as the “deployment of gene therapy for the purpose of eliciting a vaccine response,” and while the application gene therapy technology (of which mRNA technology is a subset) to vaccines holds great potential, the way the authorities went about it was nothing short of disastrous.

Conventional clinical trials for vaccines historically take about a decade, he explained, and can cost $10,000 to $20,000 per patient, and require careful monitoring of tens of thousands of vaccinated subjects in order to identify adverse reactions. What’s more, separate manufacturing facilities must be constructed for each different vaccine, further exacerbating costs.

In theory, Malone said, applying gene therapy technology to vaccines could mitigate the latter consideration by allowing the same manufacturing processes to be used to make a variety of vaccines through the insertion of different genetic “payloads” into a standard gene therapy vector (delivery system). 

This would also potentially allow for vaccines to be developed much more quickly for new diseases, as soon as a pathogen is identified, sequenced, and any potential immunogenic proteins within it are identified.

In practice, however, “the way this was deployed, obviously we threw ethics right into the trash can,” Malone said. “Everything that we had agreed upon, all of the regulatory logic that had been built over decades globally, was disregarded in this mad rush to develop a countermeasure for a pathogen that was grossly oversold, weaponized, and used to drive fear. We now know, and we knew then. We didn’t know right at the start because of a massive propaganda campaign.”

“The mRNA technology that was advanced was rushed,” he said. “We now know, for instance, that the purification of the plasma DNA that’s used to manufacture the RNA was very poor. We clearly had DNA contamination which was adulteration in these products and should negate the use of these products in humans.”

“Manufacturing processes haven’t been developed and there’s a lot of information coming out from the US, from, from the Max Planck Institute in Germany, that many of these batches were not as advertised, and we’ve been prevented from doing lot release analysis,” Malone went on. “But underlying all of that, these products … do not provide protection against infection, they do not prevent infection, they do not prevent disease, they do not prevent spread, they do not prevent hospitalization, they do not prevent death. And the latest data is for these hyper-immunized, hyper-inoculated individuals, they actually exacerbate the risks of individuals developing disease or death because they damage the immune system.”

The COVID vaccines were developed and released under former President Donald Trump’s Operation Warp Speed initiative in a fraction of the time vaccines usually take, and since then have been intensely controversial due in large part to a significant body of data linking them to various harms.

The federal Vaccine Adverse Events Reporting system (VAERS) reports 35,611 deaths, 206,108 hospitalizations, 20,380 heart attacks, and 27,307 myocarditis and pericarditis cases as of July 14, among other ailments. An April 2022 study out of Israel indicates that COVID infection itself cannot fully account for the myocarditis numbers, despite common insistence to the contrary.

Jab defenders are quick to stress that reports submitted to VAERS are unconfirmed, as anyone can submit one, but U.S. Centers for Disease Control and Prevention (CDC) researchers have recognized a “high verification rate of reports of myocarditis to VAERS after mRNA-based COVID-19 vaccination,” leading to the conclusion that “under-reporting is more likely” than over-reporting.

Further, VAERS is not the only data source containing red flags. Data from the Pentagon’s Defense Medical Epidemiology Database (DMED) shows that 2021 saw drastic spikes in a variety of diagnoses for serious medical issues over the previous five-year average, including hypertension (2,181%), neurological disorders (1,048%), multiple sclerosis (680%), Guillain-Barre syndrome (551%), breast cancer, (487%), female infertility (472%), pulmonary embolism (468%), migraines (452%), ovarian dysfunction (437%), testicular cancer (369%), and tachycardia (302%).

Last September, the Japanese Society for Vaccinology published a peer-reviewed study conducted by researchers from Stanford, UCLA, and the University of Maryland, which found that the “Pfizer trial exhibited a 36% higher risk of serious adverse events in the vaccine group” while the “Moderna trial exhibited a 6% higher risk of serious adverse events in the vaccine group,” for a combined “16% higher risk of serious adverse events in mRNA vaccine recipients.”

In December 2022, Republican U.S. Sen. Ron Johnson of Wisconsin hosted a roundtable discussion during which civil rights attorney Aaron Siri detailed data from the CDC’s V-Safe reporting system revealing that 800,000 of the system’s 10 million participants, or approximately 7.7 percent, reported needing medical care after COVID injection. “Twenty-five percent of those people needed emergency care or were hospitalized, and another 48 percent sought urgent care,” Siri added. “Also, another 25 percent on top of the 7.7 percent reported being unable to work or go to school.”

Another study by a team of American, British, and Canadian researchers, published last December by the in the Journal of Medical Ethics, found that COVID booster mandates for university students – a relatively healthy group at relatively low risk from the virus – do far more harm than good: “per COVID-19 hospitalisation prevented, we anticipate at least 18.5 serious adverse events from mRNA vaccines, including 1.5–4.6 booster-associated myopericarditis cases in males (typically requiring hospitalisation).”