Details forced out for Astra Zeneca’s Phase 3 clinical trials – ICAN to the rescue, the ICANT UK Government instead bestowed “honours” on inventors of weapons that cause carnage
In yesterday’s post here:
I bemoaned the fact that there was little known about the details of the Astra Zeneca Phase 3 clinical trials.
“There has been hardly any coverage at all for the Astra Zeneca viral vector injection clinical trials – though we know now that the EUDRA system has 4-5 times the number of reports of death following the roll-out of this injection compared to the disastrous mRNA injections of Pfizer and Moderna. This lack of coverage probably resulted because Astra Zeneca did not receive Emergency Use Authorization in the US and Astra Zeneca was content to capture large slices of markets in the UK, the EU (initially), Australasia and the sub-continent. “
Turns out efforts had been in train by Del Bigtree and Aaron Siri’s team at ICAN and HighWire since April 2022!
Here is the ICAN press release:
“Not satisfied by this complete lack of transparency, ICAN, through its attorneys, submitted an information request to the United Kingdom’s FDA equivalent – the Medicines and Healthcare Products Registry Agency (MHRA) — in April 2022 seeking information relating to its authorization of the AstraZeneca COVID-19 vaccine, as well as that relating to its authorization of the Janssen, Moderna, and Pfizer COVID-19 vaccines. “
Lots of embedded links in that last paragraph in the press release.
The fantastic team at Expose.com picked up the story here:
“On Monday, ICAN obtained confirmation of disturbing information about Oxford-AstraZeneca’s covid “vaccine” from the UK’s Medicines and Healthcare Products (“MHRA”).”
“..MHRA finally provided 166 pages of records containing the studies MHRA relied on to authorise AstraZeneca’s covid injection for use en mass.
One of these records was a study on mice which investigated the biodistribution of the AstraZeneca “vaccine.” It revealed that the viral vector DNA did not remain localised in the injection site but instead migrated to other organs. Disturbingly, the study found vector DNA in the sciatic nerves, bone marrow, livers, lungs, and spleens of the mice following vaccination.”
So, not the brain, heart and kidneys as with the mRNA injections. (I still do not apply the term “vaccines” to these injections. No-one receiving these injections has been “vaccinated”). This seems a little odd, especially in light of the below that indicates mRNA instructions to produce the spike protein.
Informed readers can help me out here. In my mind, instructing the body to produce a poisonous toxin (spike protein) is not a great idea. You want the equivalent of an anti-venom (IgG3 antibodies?) that has been cultivated in an external host, in a similar process as that used to create anti-venom to treat snake-bite? Answers on a post-card please, or use the comment section below!
Back to the Freedom of Information release:
“..AstraZeneca took these DNA genetic instructions and placed them inside another virus – a chimpanzee adenovirus. This adenovirus had been modified so that it could enter human cells but not replicate inside them or cause disease. However, once in a human cell, it could deliver its payload – the DNA instructions.
The DNA is pushed into the nucleus of the human cell where the instructions can be read. Using these instructions, the nucleus of the cell creates messenger RNA (mRNA) before pushing it out for other cell molecules to “read”.
Same risks to pregnant women (birthing persons?) and to the immune-compromised but the Astra Zeneca at least does not have the toxic lipid nano-particle delivery system (or the PEG coating?) instead using an attenuated chimpanzee virus.
“So, as with the Pfizer and Moderna vaccines, the AstraZeneca vaccine has now asked the human cell to begin translating the mRNA and build spike proteins. These coronavirus spike proteins are built and expressed on the outside of the human cells which then cause an immune response. Antibodies are trained to recognise the spikes and killer T cells try to destroy any cells containing these new instructions.”
So, what did the UK Government instruct the Queen to do about the inventors of the toxic treatment? Well, in its own tried and trusted method for covering up any wrong-doing or ineptitude, it did this:
CEO of AstraZeneca gets knighted and says Vaccine concerns were Overblown (substack.com)
And this:
Clown world.
I wonder who has been inspecting Astra Zeneca’s manufacturing plants and the sites where people got injected to ensure that the doses injected were the same as the doses in the Phase 3 clinical trials – you know, ensuring quality of conformance and compliance amongst say 1 in 1,000 vials?
I cannot confirm this, but I believe that Astra Zeneca’s injections were widely used in India when this was going on:
Onwards!
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Thank you ... shared. Good post.
Astrazeneca WAS NOT PULLED simply RENAMED: https://www.brusselstimes.com/news/eu-affairs/162559/astrazeneca-vaccine-now-renamed-as-vaxzevria-ema-european-eu-uk-swedish-lakemedelsverket