Parsing the "data" from Moderna's selective leaks to the press about its failed clinical trial in kids under 6
The shot made no difference against Covid but it does cause myocarditis and came with a 15% to 17% adverse event rate. Meanwhile the CDC admits that 74.2% of kids already have natural immunity.
On Friday, the NY Times and other stenographers for the cartel breathlessly announced that Moderna has asked the FDA to authorize its junk science mRNA shot in kids under 6. Oh, so that means Moderna submitted an application to the FDA? Well, not exactly. From the article:
“A top official at the company said it would finish submitting data to regulators by May 9.”
Wait, so Moderna is “asking” the FDA to authorize its product but Moderna will not even finish its application for another 10 days!? That’s weird. It’s like a kid asking his teacher for a A+ while his homework assignment is half-finished.
So already we’re seeing serious red flags and we’re not even out of the first paragraph.
Of course it gets worse.
To be clear, there is no data because Moderna has not even finished its application. But Moderna and the White House have been selectively leaking numbers to the press that dutifully prints them without question — and those numbers tell us that Moderna’s clinical trial was a disaster.
I need to provide some background and context and then I’ll get into the particular details about this failed clinical trial in kids.
Moderna applied for Emergency Use Authorization to administer its mRNA shot to adolescents 12 to 17 years old back on June 10, of 2021. But the application has been held up ever since. Why? Myocarditis. From the Wall Street Journal:
The Food and Drug Administration is delaying a decision on authorizing Moderna Inc.’s mRNA Covid-19 vaccine for adolescents to assess whether the shot may lead to heightened risk of a rare inflammatory heart condition, according to people familiar with the matter.
Moderna has at least two big problems in giving this shot to teenagers:
1.) The dose they are giving to teenagers is the same dose as that given to adults — 100 mcg of mRNA — which is 3.3 times the amount in the Pfizer shot given to adults (30 mcg). So the Moderna shot is great at generating antibodies that target the spike protein of the original Wuhan lab leak strain. But some of that mRNA can migrate to the heart and generate myocarditis as well. Remember, Pharma’s capture of the FDA is so extreme, they should just be able to write “Iz Gud!” on a paper napkin and the FDA will approve it — as they did with Pfizer’s application to inject kids 5 to 11 — in spite of ZERO evidence supporting this use. So if the FDA has held up Moderna’s application in teens for nearly a year, the myocarditis signal must be truly terrifying.
2.) Nordic countries are slightly less corrupt than the United States. Finland, Sweden, Denmark, and Norway have all suspended the use of the Moderna mRNA shot in teenagers because its leads to myocarditis. (Finland and Sweden even suspended its use in men under 30 years old.) Even the criminally corrupt European Medicines Agency acknowledged that both Pfizer and Moderna mRNA shots lead to myo- and pericarditis and added a warning to the product insert.
Okay what do we know about Moderna’s clinical trial in kids under 6?
Back on March 23, Moderna put out a press release claiming that:
vaccine efficacy in children 6 months to 2 years was 43.7% and vaccine efficacy was 37.5% in the 2 to under 6 years age group.
The NY Times of course printed that like it was a clay tablet handed directly from God to Moses just as they printed the “90% to 100% effective(TM)” lie in connection with the clinical trial in adults. By now everyone knows that the actual vaccine effectiveness is zero or even negative after 6 months.
Sane people pointed out that vaccine efficacy of 43% and 37% are BELOW the 50% threshold required for FDA authorization (see page 14). It’s not clear why the geniuses at Moderna did not realize this — perhaps they just wanted to rub everyone’s noses in the sheer criminality of their enterprise?
But somewhere between March 23 and last Friday, Moderna staff got the message so they did what they always do, they just manipulated the data. From the NY Times:
Moderna said Thursday the vaccine appeared to be 51 percent effective against symptomatic infection among those younger than 2, and 37 percent effective among those 2 to 5.
Okay first off, lol that they still cannot get the number above 50% in kids 2 to 5 even when they are just straight up lying about the numbers. But how did they convert 43% to the magical 51% in kids 0 to 2? They simply deleted data that they did not like:
Those results were slightly better than the ones Moderna previously released for children under 2. The company said that was because the second time, the firm excluded infections that had not been confirmed with a P.C.R. test analyzed in a laboratory.
Let’s be clear — this is Moderna’s clinical trial. They control the whole process. If you’re a study participant who is having a heart attack in the middle of the night and call 911 and go to the hospital — they kick you out of the clinical trial for not seeing their doctors and following their protocol. So Moderna is the one who makes the decision as to whether to use “a P.C.R. test analyzed by a laboratory.” To now exclude (without any valid justification) infections that made their clinical trial look bad is gross scientific misconduct. The Moderna application, when/if it is submitted 10 days from now, should be rejected immediately because of this misconduct.
While the clinical trials in kids were failing, Pfizer and Moderna were running a half-hearted campaign to pressure the FDA to approve these shots in kids under 5 — in spite of zero data showing benefit and considerable evidence showing harms. The attempts were pathetic and included hashtags on social media like #immunizeunder5 that were likely only used by people taking money from these monsters. But of course the stenographers eagerly reported on this milquetoast effort and one of the talking points is, ‘well, okay, the shots do not meet the required 50% FDA threshold but some protection is better than none(TM) so please authorize my right to genocide my kids.’
Well, it turns out, these shots do NOT even offer “some protection”:
Moderna’s clinical trial data showed that the antibody response of the youngest children compared favorably with that of adults ages 18 to 25, meeting the trial’s primary criterion for success. Although the trial was not big enough to measure vaccine effectiveness…
What!? “The trial was not big enough to measure vaccine effectiveness.” Isn’t that the whole point of a clinical trial!? So Moderna (and the NY Times) are saying that the clinical trial made ZERO difference on Covid-related health outcomes including infection, hospitalization, ICU visits, or deaths, because the SARS-CoV-2 virus is not a threat to healthy children in this age group — which we have been pointing out for months.
So how does Moderna try to finesse it? They look at antibodies in the blood, not health outcomes in the real world. They call it “immunobridging”. As I explained at length back in October, this is NOT a scientifically valid way to use immunobridging (claiming likely future health outcomes from antibodies alone when the trial showed no such thing). Immunobriding is only valid if one has clinically validated correlates of protection and conditions prevent one from conducting a proper RCT (neither of which apply in this case).
Even the hand-picked yes-men and women on the CDC’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) acknowledged at their last meeting that they do NOT have “correlates of protection” that would enable them to estimate health outcomes from antibody measures. Eric Rubin (Editor-in-Chief of the NEJM) even stated, “We know what kind of antibody response can be generated, we just don’t know if it works.”
So Moderna is asking the FDA to authorize its mRNA shot in kids under 6 based on antibodies alone even though every member of the FDA’s VRBPAC acknowledges that antibodies tell you absolutely nothing about likely health outcomes.
(In fact, new evidence suggests that mRNA shots suppress the body’s innate ability to generate anti-N antibodies.)
What about side effects?
Side effects were at a similar level as those from previously approved pediatric vaccines, with fevers in 15 percent to 17 percent of the children, Moderna said.
Any shot with an adverse event rate over 1% should not be authorized. To authorize a shot with a 15 to 17% adverse event would be batsh*t insane.
Furthermore, we know that Moderna and Pfizer make cases of disability and death in their clinical trials disappear — so the actual adverse event rate is surely even higher than 15% to 17%.
Making this nightmare complete, the CDC acknowledged on April 26, 2022, that 74.2% of children ages 0 to 11 are already naturally immune to Covid-19 because of prior exposure. The 74.2% number came from February, so given the rate of increase at the time, by now nearly 100% of children ages 0 to 11 likely already have natural immunity which is superior to artificial vaccine immunity. There is no emergency in this population that would justify an emergency use authorization of this useless toxic product.
So to recap this painful saga:
• Moderna shots cause myocarditis and pericarditis which is why Moderna has not been able to get authorization to inject mRNA into teenagers.
• Moderna shots make no difference in connection with Covid-19 in this age group.
• Moderna shots come with at least a 15% to 17% adverse event rate.
• Nearly all children in this age group are already naturally immune so there is no emergency that would justify an emergency use authorization.
This is not hard to figure out. In a sane world this application would be dead on arrival, whenever Moderna gets around to actually turning in its application. Any reporter worth his/her salt should be ridiculing Moderna’s weird mix of hubris, incompetence, bad “data”, and malevolence. But our country, its “public health” agencies, and the mainstream media are run by Insane Nazi Clowns. I imagine many bougiecrats will drown in their own tears if they are not allowed to genocide their own kids with this shot (and then they’ll celebrate their sacrifice and take selfies with their kids in the ICU when the myocarditis kicks in, proclaiming #getvaccinated). Of course bougiecrats can already get this shot for their kid off label, so my hunch is that it’s really your kids who they want to genocide.
In future articles I’ll have additional thoughts about how we push back. In the meantime, this continues to be our best play and I encourage all of us to just get into the habit of contacting 25 people at the FDA every day to tell them to REJECT both the Moderna and Pfizer applications to inject mRNA into little kids.
Blessings to the warriors. 🙌
Prayers for the truth tellers. 🙏
In the comments, please let me know what’s on your mind.
(As always, please help me catch any typos.)
Photo credit for the thumbnail illustration: Daniel Zender.
Thank you for clearly documenting this atrocity. Sorry, if I overlooked this but could you let me know where I can find a link to the protocol that says a trip to the ER could be censored from the trial if the investigators are not contacted first?
Ah, good times. Making a "vaccine" is like being a weatherman: You can be wrong all the time and still get paid.
The FDA’s top vaccine leader told a congressional committee on Friday afternoon that although the adult vaccines had to meet a 50% threshold for efficacy against Covid-19 infections, that same standard will not need to be met for the vaccines for the youngest group of children, for which a vaccine is not yet available.
[...] According to a readout of the meeting from the House select subcommittee on the coronavirus crisis, Marks explained that the FDA would not withhold authorization — despite previous guidance — for a pediatric vaccine solely because it did not reach a 50% efficacy threshold at blocking symptomatic infections. All of the other adult and children’s vaccines currently authorized in the US have lost significant amounts of efficacy due to the Omicron variant, but they still remain effective at reducing the risk of severe disease, hospitalization and death.
“If these vaccines seem to be mirroring efficacy in adults and just seem to be less effective against Omicron like they are for adults, we will probably still authorize,” Marks said.
How can they "protect against severe disease and death" in children younger than five when these kids aren't dying? And 75% of them (probably more) have already had the "disease"? Going to bang my head on the wall for a while.