Another win for Big Pharma. Another betrayal of the public trust.
A Legal and Ethical Breach
The FDA has once again bent the knee to pharmaceutical giants. In a stunning move, it approved Moderna’s new COVID-19 injection—mNEXSPIKE (mRNA-1283)—without a placebo-controlled trial. This reckless decision violates not just science, but a recent legal promise by the U.S. Department of Health and Human Services (HHS).
Just weeks ago, HHS publicly pledged:
“All new vaccines will undergo safety testing in placebo-controlled trials prior to licensure — a radical departure from past practices.”
Now, the FDA has tossed that promise aside. It’s business as usual in Washington, where profit still outranks principle.
The Shot No One Asked For
mNEXSPIKE is Moderna’s latest gamble—a “next-gen” COVID shot targeting only fragments of the spike protein. Not the full spike. Just the RBD and NTD portions. The company claims it’s more effective.
But where’s the proof?
There’s no placebo group. No baseline comparison. Moderna simply measured it against their earlier shot—a vaccine already associated with thousands of reported injuries and deaths.
This is not medicine. This is marketing.
Who’s Getting It? Almost Everyone
The FDA approved mNEXSPIKE for:
- Anyone 65 and older
- Anyone 12 to 64 with a CDC-listed “underlying condition”
That’s most of the adult population. Conditions like anxiety, obesity, or asthma qualify. Essentially, the door is wide open.
Tens of millions are now eligible for an experimental shot with no real safety data. This isn’t public health. It’s population-wide testing without consent.
The Trial Starts Years After Approval
Moderna’s real placebo-controlled trial? It won’t start until November 2025. Results? Not until 2027.
That’s two more years of blind trust. Two more years of potential harm. Two more years of zero accountability.
This is regulatory malpractice.
Big Pharma’s Grip on the System
The decision isn’t just irresponsible—it’s revealing. A recent article in the New England Journal of Medicine, co-authored by government insiders, outlines a new “evidence-based” strategy. In truth, it’s a smokescreen.
It gives bureaucrats and corporations legal cover to skip proper trials and flood the market with mRNA products—no matter the risk.
These agencies have stopped protecting the public. They now protect profits.
Losing Trust by Design
Americans are waking up. COVID mandates, secret deals, and a lack of liability have already shattered public trust. This latest move confirms what many feared:
The pandemic was a gold rush for Big Pharma.
Safety standards are now optional. Transparency is gone. Laws are broken without consequence.
The COVID Cartel
What do you call it when a federal agency knowingly greenlights a product without adequate testing?
Fraud.
The FDA, Moderna, and their partners in government have crossed a line. They’ve ignored scientific norms. They’ve violated their own policy. And they’ve treated the American people as test subjects.
This isn’t just unethical. It’s criminal.
Final Thought
Until Moderna’s placebo trial ends in 2027, millions will serve as guinea pigs. Injuries will go uncounted. Accountability will remain a fantasy.
And the FDA will keep smiling.
The COVID machine rolls on.
Fueled by fear. Driven by profit. Enabled by silence.
It’s time to call it what it is—a coordinated scam at the highest levels of health and power.
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