Here's the headline of the lead story in Tuesday's New York Times.* Click on the link, and
read that article about the "promising early results" of Moderna's test of its coronavirus
vaccine.
Then read the commentary (just below) that Robert Kennedy, Jr. posted yesterday on
Instagram (the only "social media" forum he's allowed to use in this "democracy").
From reading both those pieces, you will learn that "America's newspaper of record"
is as reliable an outlet as Pravda under Stalin, or the Frankfurter Zeitung under Dr.
Goebbels. Just note the discrepancy between the Times' upbeat reference to the
"8 healthy volunteers" participating (and doing really well!) in Moderna's test, and
the "15 human guinea pigs" subjected to it—three of whom (to continue quoting
Kennedy, who quotes Moderna's press release) "suffered a 'serious adverse event'
within 43 days of receiving Moderna's jab."
How long can this go on, before even that newspaper's most devoted readers see
that it's every bit as credible as Donald Trump?
MCM
*That's the online headline. The headline in the paper paper: "Vaccine's Early
Test Result Elevates Hopes and Stocks."
Despite Moderna’s cheery press release [Monday] morning, the clinical trial results for its groundbreaking
COVID vaccine could not be much worse. The vaccine, developed and championed by Anthony Fauci
and financed by Bill Gates, used an experimental MRNA technology that the two men hoped would allow
rapid deployment to meet President Trump’s ambitions “warp speed” time line. Dr Fauci was so confident
of his shot’s safety that he waived ferret and primate studies. (Moderna suspiciously reported no health
data from its mouse studies.)
That appears to have been a mistake. Three of the 15 human guinea pigs in the high dose cohort (250 mcg)
suffered a “serious adverse event” within 43 days of receiving Moderna’s jab. Moderna did not release its
clinical trial study or raw data, but its press release,which was freighted with inconsistencies, acknowledged
that three volunteers developed Grade 3 systemic events defined by the FDA as “Preventing daily activity and
requiring medical intervention." Moderna allowed only exceptionally healthy volunteers to participate in the
study. A vaccine with those reaction rates could cause grave injuries in 1.5 billion humans if administered
to “every person on earth”. That is the threshold that Gates has established for ending the global lockdown.
Moderna did not explain why it reported positive antibody tests for only eight participants. These outcomes
are particularly disappointing because the most hazardous hurdle for the inoculation is still ahead: challenging
participants with wild COVID infection. Past attempts at developing COVID vaccines have always faltered at
this stage, as both humans and animals achieved robust antibody response, then sickened and died when
exposed to the wild virus.
Moderna’s press announcement heralded “Positive Interim Phase 1 findings.” I have forwarded that claim to
my colleagues in securities law. FTC rules restrict the amount of lipstick public companies may slather on
bad donkeys.