05/29/2025 / By Lance D Johnson
In a stunning reversal, the U.S. government has abruptly terminated a $700 million contract with Moderna to develop an mRNA-based bird flu vaccine — raising urgent questions about whether this signals an end to pandemic fearmongering or merely a shift toward even riskier genetic injection technologies. While the cancellation offers a temporary reprieve from Moderna’s predatory vaccine schemes, skeptics warn that the vaccine industry may still be pushing forward with experimental “self-amplifying mRNA” (sa-mRNA) shots, a technology that forces the body to mass-produce viral proteins indefinitely.
Key points:
Moderna’s financial survival has long depended on taxpayer-funded vaccine contracts, particularly after its COVID-19 shots — linked to heart damage, immune disorders and excess deaths — failed to secure long-term market demand. With plummeting stock prices and dwindling public trust, the company has aggressively lobbied governments to bankroll new pandemic threats, including avian influenza.
The now-canceled H5N1 contract was part of a broader push by the Biomedical Advanced Research and Development Authority (BARDA), an HHS agency notorious for funneling billions into Big Pharma’s experimental projects. Moderna had already received $176 million in 2023 to fast-track its mRNA bird flu shot, despite zero long-term safety data.
“These clinical data in pandemic influenza underscore the critical role mRNA technology has played as a countermeasure to emerging health threats,” Moderna CEO Stéphane Bancel claimed in a press release — a statement that ignores the thousands of injuries reported from COVID-19 mRNA shots.
While the cancellation appears to be a setback for Moderna, the government has not abandoned its pandemic preparedness agenda. Instead, federal agencies are quietly shifting toward even more experimental platforms, including self-amplifying mRNA (sa-mRNA) vaccines. Unlike traditional mRNA shots, which degrade quickly, sa-mRNA injections hijack the body’s cells to continuously produce viral proteins — a process with unknown long-term consequences.
In November 2023, FDA approved its sa-mRNA bird flu vaccine, ARCT-2304, signaling a dangerous new frontier in genetic experimentation. Meanwhile, the U.S. Government Accountability Office (GAO) confirmed plans for a “universal flu vaccine” trial in 2026, raising fears that synthetic, multi-strain injections could trigger catastrophic immune responses.
The abrupt cancellation of Moderna’s contract does little to address the root of the problem: government-funded gain-of-function research that artificially engineers pandemic threats. Since early 2024, the USDA has been conducting high-risk experiments on H5N1 viruses — potentially enhancing their transmissibility — while simultaneously developing mRNA “solutions” for the very pathogens they helped create.
This corrupt cycle mirrors the COVID, where taxpayer-funded research at the Wuhan Institute of Virology preceded a global pandemic and unprecedented vaccine windfalls for companies like Moderna.
Despite the contract termination, Moderna shows no signs of retreating. The company recently opened a 290,000-square-foot U.K. facility capable of churning out 250 million vaccines annually, suggesting it still expects lucrative government contracts.
For those who have witnessed the devastation of COVID-19 mandates, the cancellation is a small victory—but the war is far from over. Until gain-of-function research is banned and vaccine manufacturers are held legally accountable for injuries, the medical police state will continue exploiting public health crises for profit.
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Tagged Under:
BARDA, Biden administration, bird flu, gain-of-function, genetic lunacy, H5N1, HHS, Moderna, mRNA vaccines, pandemic, pharmaceutical fraud, public health corruption, research, sa-mRNA, self-amplifying mRNA, Universal Flu Vaccine, Vaccine injuries
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