This is what Health Canada (Canadian FDA) and Novavax think is an appropriate level of transparency when,
Seeking all documents, datasets, spreadsheets, papers, presentations, email communications, attachments, and other digital materials - excluding bulk clinical data findable via the Clinical Information Release system - to date between (to and from) Novavax Inc and Health Canada with regard to the Novavax COVID-19 vaccine, also known as NVX-CoV2373, also known as SARS-CoV-2 rS (recombinant spike) protein nanoparticle vaccine with Matrix-M1 adjuvant. Please include the Nonclinical Study Reports, Nonclinical Overview and the Safety Evaluation from the Clinical Study Reports.
The official response?
An 8,313 page pdf, almost entirely redacted.
Safe, effective, and hiding in the shadows.
9 deaths in the vaccine arm of Novavax’s trial occurred, with no circumstances divulged publicly. As of writing, ‘regulators’ at the WHO, EU and in SK have already authorized it fit for human injection. Gates loves Novavax.
In the package, you’ll find not a shred of technical data about this most questionable of products. Why the extreme secrecy?
Some pages of interest:
p. 305: invoice
p. 1914: drug submission form
p. 1955: consent to share regulatory info, international regulators are noted (readers in these jurisdictions can file data requests)
There are some interesting pages from 1197 to 1384, and 1568 to 1642, but these are old regulatory documents
Quoting the U.S. judge who ordered FDA/pfizer to release data @ 55k pages/month:
As James Madison wrote, “[a] popular Government, without popular information, or the means of acquiring it, is but a Prologue to a Farce or a Tragedy; or, perhaps, both. Knowledge will forever govern ignorance: And a people who mean to be their own Governors, must arm themselves with the power which knowledge gives.”
John F. Kennedy likewise recognized that “a nation that is afraid to let its people judge the truth and falsehood in an open market is a nation that is afraid of its people.”
stay tuned
You’re getting a lot more public information than we got in U.K.
The MHRA called a press conference to tell us that they’d granted the Pfizer / BioNTech product an emergency use authorisation or whatever nebulous term they’d chosen for unleashing a hopelessly under characterised agent on the public.
The “top line report” came via a press release from Pfizer.
Later, an obviously fraudulent clinical trial was published in a journal. That’s it. I’ve no idea what’s actually in the vials. Given evident regulatory capture, it’s possible almost no one knows.