Post by fearnot on Sept 1, 2022 12:45:34 GMT -5
Moderna Vaccine Trials Contained ‘Mostly Irrelevant Studies’
and ‘Deceptive Practices’:
Veteran Pharma Analyst
Do not be deceived,
my beloved brethren.
James 1:16
Moderna’s internal documents regarding their COVID vaccine trials,
obtained via a Freedom of Information Act
request by Judicial Watch,
show that most of their studies submitted for approval to the FDA were
“irrelevant” and did not follow Good Laboratory Practices (GLP),
according to a former pharma executive.
“Moderna claimed that the active substance mRNAs
of SPIKEVAX
does not need to be studied for toxicity
and can be replaced with any other mRNA
without further testing,”
“The FDA did not push back on this preposterous claim.
The company is claiming that the active drug substance
of a novel medicine
does not need to be tested for toxicity.”
Latypova has worked in more than 60 pharmaceutical companies
mainly focusing on creating and reviewing clinical trials,
many of which were submitted to the FDA.
According to her research, Moderna
skipped entire categories of safety and toxicology testing.
Moderna used substitute test articles,
and used other deceptive study design practices,
such as
stopping the studies early,
while the drug was still accumulating in major organ systems
and
not studying the expression of the target antigen (spike protein)
in the organs where the drug was being delivered,”
Latypova said.
Latypova further noted that there was
“no Safety Pharmacology,
Metabolism,
Carcinogenicity,
Genotoxicity
or Drug Interaction studies were done for Spikevax
as a complete final product
as dispensed to millions of patients today
www.theepochtimes.com/moderna-vaccine-trials-contained-mostly-irrelevant-studies-and-deceptive-practices-veteran-pharma-analyst_4689239.html