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Moderna’s 2013 patent on furin cleavage site, Brook Jackson’s 2020 report to FDA on clinical trial fraud, Pfizer 2021 SEC filings...
First pass at a timeline. Working on a full, long-form report. Will update this to fix typos, add links, etc.
tl; dr - Pfizer defrauded the US Government through the clinical trials for the pharmaceutical product sold to and marketed by the US government as a “safe and effective Covid-19 vaccine;” the US Government knew it was being defrauded no later than Sept. 17, 2020; the US Government covered up the fraud for Pfizer and continued to purchase, market and mandate the fraudulent, deadly and ineffective pharmaceutical product.
2013/12/16 - Moderna filed four US patent applications for the genetic sequence of the furin cleavage site that later appeared in Covid-19. US9149506B2; US9216205B2; US9255129B2; US9301993B2. Source: Frontiers in Virology paper, 2/21/22, Ambati et al, MSH3 Homology and potential recombination link to SARS-CoV-2 Furin cleavage site; DailyExpose.uk, 3/14/22
2016/02/04 - Moderna filed one US patent application for the genetic sequence of the furin cleavage site that later appeared in Covid-19. US9587003B2. Source: Frontiers in Virology paper, 2/21/22, Ambati et al, MSH3 Homology and potential recombination link to SARS-CoV-2 Furin cleavage site; DailyExpose.uk, 3/14/22
2019/12 - Bill Gates tweet, “bullish” on vaccines. Source: Edward Dowd testimony to People’s Grand Jury, Coronavirus Investigating Committee, Reiner Fuellmich, 2/25/22.
2020/04/05 - James Bullard, Federal Reserve Bank president, on Face the Nation, states that economy will emerge from Covid-19 panic using digital vaccine passports and digital currency. Source: Edward Dowd testimony to People’s Grand Jury, Coronavirus Investigating Committee, Reiner Fuellmich, 2/25/22.
2020/05 - President Trump begins process of blocking US funding for World Health Organization and suspending US membership, over concerns about China’s obstruction, fraud and manipulation during Covid-19 crisis. Source: CNN.
2020/07/08 - President Trump formally notifies World Health Organization of US intention to withdraw in one year (by July 2021). Source: NBC News.
2020/09 - Brook Jackson hired by Ventavia as regional manager of Phase 3 clinical trials of Pfizer’s Covid-19 pharmaceutical product, Fort Worth and Keller, Texas. Jackson observes numerous clinical trial safety and protocol violations. Jackson collects internal emails and other documents providing evidence that Ventavia officials knew of the violations and conveyed them to Pfizer as early as August 2020, but did not stop enrollment or halt the studies. Jackson reported the violations to Ventavia officials, discussed it with them and recorded conversations. Enrollment and trials continued. Source: British Medical Journal report by Paul Thatcher, 11/2/21; Brook Jackson testimony to People’s Grand Jury, Coronavirus Investigating Committee, Reiner Fuellmich, 3/4/22.
2020/09/25 - Jackson reported the clinical trial violations to US Food and Drug Administration, requesting investigation and halt to the study. She was fired by Ventavia several hours later. Source: British Medical Journal report by Paul Thatcher, 11/2/21; Brook Jackson testimony to People’s Grand Jury, Coronavirus Investigating Committee, Reiner Fuellmich, 3/4/22.
2020/09/29 - Brook Jackson’s last contact with USFDA officials. Enrollment and trials continued. Source: Brook Jackson testimony to People’s Grand Jury, Coronavirus Investigating Committee, Reiner Fuellmich, 3/4/22.
2020/10/09 - Mark Barnes, attorney for Pfizer, contacts Brook Jackson on her personal cell phone by text and phone call. Further evidence of Pfizer corporation’s knowledge of fraud. Source: Brook Jackson testimony to People’s Grand Jury, Coronavirus Investigating Committee, Reiner Fuellmich, 3/4/22.
2020/11 - Pfizer submits to FDA “Phase 1/2/3, placebo-controlled, randomized, observer-blind, dose-finding study to evaluate the safety, tolerability, immunogenicity and efficacy of SARS-CoV-2 RNA vaccine candidates against Covid-19 in healthy individuals.” Study has not and will not assess pharmacokinetics, pharmacodynamics, biomarkers or genetics. Source: Pfizer submission at page 72.
2020/12 - US Government’s Covid-19 “vaccine” marketing and mandate campaign launched. US government tells Americans shots are “safe and effective.” Millions of Americans injected, many fatally. Hundreds of thousands endure debilitating adverse effects in first year after injection alone. US government will not acknowledge their injuries or investigate. Doctors, nurses, scientists, attorneys attempt to warn Americans. Punished with job loss, comprehensive censorship/legacy media blacklisting and reputational damage. Sources: Steve Kirsch, Jessica Rose, Alex Berenson, Robert Malone, Peter McCullough, Byram Bridle, Mike Yeadon, Bret Weinstein, many more.
2021/01/08 - USA v. Ventavia, Pfizer and Icon corporations filed in Texas by US government on behalf of whistleblower Brook Jackson, under False Claims Act, 31 USC 3729. Case No. 1:21-CV-00008-MJT.
[Brook Jackson] observed:
fabrication and falsification of blood draw information, vital signs, signatures and other essential clinical trial data;
enrollment and injection of ineligible clinical trial participants, including Ventavia employees’ family members;
failure to timely remove ineligible patients’ data from the trial;
failure to maintain temperature control for the vaccine at issue;
failure to monitor patients after injection as required by the trial protocol;
principal investigator oversight failures;
use of unqualified and untrained personnel as vaccinators and laboratory personnel;
failure to maintain the “blind” as required, which is essential to the credibility and validity of the observer-blinded clinical trial;
ethical violations, such as failure to secure informed consent and giving patients unapproved compensation;
improper injection of the vaccine (i.e., by over-diluting vaccine concentrate or using the wrong needle size);
failure to ensure that trial site staff were properly trained as required by good clinical practices;
safety and confidentiality issues, including HIPAA violations; and
other violations of the clinical trial protocol, FDA regulations, and Federal Acquisition Regulations and their DoD supplements.
Ventavia failed to report the majority of its clinical trial protocol and regulatory violations to Pfizer or the external Institutional Review Board. Issues were improperly documented or hidden away in “notes to the file,” and not corrected.
Case sealed by judge under 31 USC 3730(b)(2). Jackson gagged — ordered not to disclose her experiences publicly. Jackson maintains her silence for 10 months under advice of her attorney (that US government will attack her if she speaks publicly). She decides that when the marketing and mandate campaign comes for her children’s age group, she will violate the gag order and speak out publicly. Source: Brook Jackson testimony to People’s Grand Jury, Coronavirus Investigating Committee, Reiner Fuellmich, 3/4/22.
2021/01/22 - Newly-installed President Biden reverses Trump’s planned withdrawal of the US from World Health Organization, restarts US funding. Source: USA Today.
2021/02 - Japanese regulatory agency obtains Pfizer clinical trial data regarding pharmacokinetics in rats, concentration of Pfizer’s product in spleen, ovaries, other major organs. Report later obtained, translated into English, and discussed publicly by Dr. Byram Bridle. See also European Medicines Agency application materials filed by Pfizer, admitting no biodistribution or pharmacokinetic studies had been conducted.
2021/02/28 - Pfizer prepares clinical trial data report “5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) received through 28-Feb-2021.” Report indicates Pfizer is tracking approximately 1,290 adverse effects experienced by human test subjects, many fatal and/or severely debilitating.
2021/04/30 - FDA receives Pfizer clinical data report “5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) received through 28-Feb-2021” Report indicates Pfizer is tracking approximately 1,290 adverse effects experienced by human test subjects, many fatal and/or severely debilitating. FDA does not disclose the information to the American public or withdraw the product from the market. US government continues to market and mandate the Pfizer product as “safe and effective,” including through $1 billion legacy media advertising campaign funded by US Health and Human Services Department.
2021/05/26 - University of Guelph vaccine scientist Byram Bridle obtains English translation of Japanese data, discusses it with Steve Kirsch and others on a Canadian Covid Care Alliance phone call, and then discusses it on Darkhorse podcast June 10, 2021 with Bret Weinstein and Robert Malone. Censorship and firing campaign against Bridle, Weinstein, Malone, Kirsch and others escalates.
2021/08/13 - 24-page report by Major Joseph Murphy, US Marine Corps, of the Defense Advanced Research Projects Agency (DARPA) Directors Office (DIRO), submitted to the Department of Defense Inspector General re: SARS-CoV-2 as manufactured chimeric virus. Report obtained and published by Project Veritas Jan. 11, 2022.
2021/08/23 - FDA “approves” Pfizer injections, in legally ambiguous form, for administration to recipients over the age of 16, allegedly removing it from “emergency use authorization” status but retaining its blanket liability shield. This move created the legal rationale for ensuing federal government (OSHA/CMS/DoD etc.) and private employer-enforced mandates: job loss for injection-refusal.
2021/09/01 - FDA announces forthcoming resignations of two vaccine regulators — Dr. Marion Gruber and Dr. Philip Krause — to be effective by Nov. 1, 2021. News reports state the resignations are in response to Biden Administration coercive pressure to approve “boosters.” During September and October, pressure rises on FDA to approve and recommend injections for children age 5-11.
2021/09/13 - Dr. Gruber and Dr. Krause publish Lancet paper recommending no universal booster policy. Source: James Cintolo Substack, 12/26/21.
2021/09/16 - Public Health and Medical Professionals for Transparency file Freedom of Information Act lawsuit against FDA, seeking clinical trial data. Case No. 4:21-cv-01058-P. Source: PHMPT.org.
2021/10/29 - FDA announces “approval” for Pfizer product to be injected into children ages 5-11.
2021/11/02 - Brook Jackson goes public, providing information to British Medical Journal reporter Paul Thacker. Jackson’s attorney at US Department of Justice ceases representing her, because she violated the gag order. Source: BMJ 11/2/21; Brook Jackson testimony to People’s Grand Jury, Coronavirus Investigating Committee, Reiner Fuellmich, 3/4/22.
2021/11/17 - First batch of Pfizer clinical trial data released in PHMPT v. FDA, including evidence of Pfizer’s Feb. 28, 2021 knowledge of severe adverse effects after just the first three months of injections, and FDA’s April 30, 2021 knowledge of same. Source: 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) received through 28-Feb-2021.
2021/11/17 - US-HHS added “SARS-CoV/SARS-CoV-2 chimeric viruses resulting from any deliberate manipulation of SARS-CoV-2 to incorporate nucleic acids coding for SARS-CoV-2 virulence factors” to the list of “biological agents and toxins listed in this section [that] have the potential to pose a severe threat to public health and safety” to 42 CFR 73.3. [NOTE: This classification change relates to Bailiwick’s long report about how US HHS is at the center of the American branch of the World Health Organization under the 2005 International Health Regulations, such that WHO already is the bankers’ one-world-government and the US government has already been rendered moot until US withdraws as a member state from WHO. US-HHS definition change may also be an attempt to forestall accountability efforts by preemptively reclassifying bioweapons as legally identical to pandemics, to block international law claims brought under the theory that SARS-CoV-2 is a bioweapon, and not a pandemic, thus nullifying the PHEIC pretext for sovereignty-removal issued by Tedros on Jan. 30, 2020 and still in effect, and instead bringing international laws prohibiting chemical and biological weapons to bear.]
2021/12/01 - Second batch of Pfizer clinical trial data released in PHMPT v. FDA.
2021/12/13 - Third batch of Pfizer clinical trial data released in PHMPT v. FDA. FDA then tries to get the court to allow documents to be released at a rate of 500 pages per month, to be completed in 75 years. Source: Aaron Siri (PHMPT attorney) Substack.
2022/01/01 - Indiana-based One America life insurance company CEO Scott Davison reports on a conference call that deaths up 40% in 18-64 age range in 2H-2021 as compared to prior years, and “uptick” in disability claims. Source: CenterSquare; Robert Malone Substack.
2022/01/06 - US District Judge Mark Pittman orders FDA to release documents at rate of 55,000 pages per month, first 10,000 due March 1, 2022. Pfizer subsequently attempted to intervene. Judge holds Pfizer request in abeyance by order dated 02/07/22.
2022/01/25 - Attorney Thomas Renz testifies before Senator Ron Johnson “Second Opinion” hearing, discloses whistleblower evidence of extremely high volume of severe adverse effects experienced by injected military personnel, under direction of Department of Defense, as documented in Defense Medical Epidemiology Database (DMED).
2022/01/30 - Attorney Todd Callender interview by Dr. Elizabeth Lee Vliet re: World Health Organization International Health Regulations of 2005, implementing federal and state regulations, US Supreme Court precedent re: patent-holder ownership of genetically modified organisms. Source: America Outloud.
2022/02/02 - Pentagon spokesmen claim five years of corrupted data in DMED database between 2016 and 2020. Over next five days, Pentagon employees backfill data to raise baseline to make 2021 spikes in diseases appear normal. Source: Daniel Horowitz reporting at The Blaze; Thomas Renz law firm.
2022/02/08 - Pfizer SEC filing, 4Q2021 and full year 2021, released. Shareholders notified in risk disclosure section, amending 3Q text, to add to risk list: “further information regarding the quality of pre-clinical, clinical or safety data, including by audit or inspection.” Source: Kelly Brown on Twitter (@rubiconcapital_) by way of Naked Emperor on Substack.
2022/02/21 - Frontiers in Virology publishes paper, MSH3 Homology and potential recombination link to SARS-CoV-2 Furin cleavage site, by Ambati et al, stating that Moderna patented the genetic sequence in 2016 [and 2013] and it was located in the US National Institutes of Health BLAST database. Evidence SARS-CoV-2 and pharmaceutical products are both designed and manufactured bioweapons.
2022/02/23 - Daily Mail UK reports on Frontiers in Virology paper, MSH3 Homology and potential recombination link to SARS-CoV-2 Furin cleavage site, by Ambati et al.
2022/02/23 - Andreas Schofbeck of BKK health insurance corporation in Germany publishes information about adverse effects of Covid-19 ‘vaccines’ as evidenced in databases of health care contacts among German population. Schofbeck then scheduled to speak to German vaccine regulator on 03//01/22, but is fired before he can attend the meeting. Source: Eugyppius Substack.
2022/02/24 - Russia invades Ukraine after provocation by NATO and United States government; targets US-funded and US-operated bioweapons facilities.
2022/02/25 - Former Blackrock investor Edward Dowd testimony to People’s Grand Jury, Coronavirus Investigating Committee, Reiner Fuellmich, re: Pfizer’s corporate fraud, stock values, etc.
2022/03/01 - Fourth batch of Pfizer clinical trial data released in PHMPT v. FDA.
2022/03/01 - German insurance executive Andreas Schofbeck, BKK, fired on the day he was scheduled to meet with German vaccine regulator.
2022/03/03 - Federal deceptive medical practice and civil rights lawsuit filed in Utah against Biden Administration, US Department of Health and Human Services, Xavier Becerra, Centers for Medicare and Medicaid Services, et al. 2:22-cv-00149 DAK.
2022/03/04 - Former Ventavia regional manager for Pfizer clinical trials Brook Jackson testifies to People’s Grand Jury, Coronavirus Investigating Committee, Reiner Fuellmich, re: Pfizer’s corporate fraud and US government’s complicity and coverup.
2022/03/07 - Thomas Renz files “Special Notice Regarding Evidentiary Findings Related to the Official Renz Law Covid-19 Investigation” including evidence related to the Department of Defense DMED database fraud. Source: Renz Law.
2022/03/07 - Pfizer files with the SEC a Form 25 - Notification of Removal from Listing and/or Registration under Section 12(b) of the Securities Exchange Act of 1934. 17 CFR § 240.12.
2022/03/13 - Dr. David Martin announces federal civil rights lawsuit filed in Utah; products are not legally vaccines. Discloses Pfizer financial documents asserting plans to license pharmaceutical product for up to 10 additional injections. Source: David Martin video 3/13/22, VigilantFox on Rumble.
2022/03/13 - Pfizer CEO Albert Bourla announces via CBS and Politico that Americans will have to get second booster/fourth injection.