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DC Mayor Muriel Bowser was questioned about her COVID-19 vaccine mandate for all public-school students aged 12 and up. A local DC journalist from The Daily Signal asks why she stands behind a policy that will disproportionately affect more than 40% of black students. TrialSite discusses her response and the DC public school's response to forcing low-income families to get the vaccine while no virtual learning option is in place for those wishing to decline.

Join The Conversation! | https://trialsitenews.com/ Last week, Greg Steube, a Republican U.S. Representative from Florida, wrote and sent a letter to FDA Commissioner Robert M. Califf demanding full compliance with laws associated with the Vaccine Adverse Event Reporting (VAERS) data and the COVID-19 vaccines. This letter was cosigned by two members of Congress, including Rep. Michael Cloud (R-Texas) and Rep. Tom Tiffany (R-Wis.)

Join The Conversation! | https://trialsitenews.com/ Twenty people who were harmed by Covid-19 vaccines came to Washington D.C. this week—sick, bereaved, from a dozen states—seeking help from the U.S. Food and Drug Administration. This is what they got: One hour with the top vaccine official in the United States—in a Zoom call to their hotel conference room. “They were hiding behind a monitor,” said Brianne Dressen, 41, a Utah mother of two who was incapacitated in a vaccine trial for which she enthusiastically volunteered in November 2020. “All of us, we came out here, and Peter Marks could not get out of his house and meet with us.”

I am learning from Dr. Michael Palmer, a physician and microbiologist from Canada about mechanisms of tissue damage by spike protein in the mRNA injections. We are looking at histopathology slides from a German pathologist Dr. Burkhard who performed autopsies on several vaccine victims.

Join The Conversation! | https://trialsitenews.com/ Dr Andrew G. Huff, former EcoHealth Alliance VP turned whistle-blower spoke exclusively to Trial Site News’ Sonia Elijah about his tenure at the controversial organization, which has been at the centre of the Covid-origin lab leak theory. Huff, who is an expert in the field of bioterrorism and biosurveillance worked at EcoHealth Alliance from 2014-2016. He reviewed the research proposal "Understanding the risk of Bat Coronavirus Emergence" that was submitted to the NIH which detailed gain of function virology work, which he attests led to the creation of SARS-CoV-2. He warned Dr Peter Daszak, his former boss, about the biosafety and biosecurity risks but Daszak was dismissive of his concerns. Huff also revealed the fact there was no biological security officer and institutional biosafety committee at EcoHealth Alliance, which was a violation of NIH guidelines.

125 million dollars is being waged in the war against diabetes, and this time it’s being sent to a biopharmaceutical company dedicated to intercepting and preventing immune-mediated disease: Provention Bio. They are looking to intervene by researching, developing, and bringing medicines to market that have the potential to help patients that would have otherwise robbed them of their full lifetime of potential. So far, they have deployed multiple candidates in conjunction with other organizations to combat these conditions. The best candidate? That would be Teplizumab.

Must watch!

Join The Conversation! | https://trialsitenews.com/ A major 90-page decision from the Fifth Circuit Court of Appeals in Louisiana represents a big victor for First Amendment, freedom of speech advocates, especially in the age of COVID-19. We are in a time when the federal government, in an unprecedented manner, freely admits to coordinating and possibly conspiring with big media and big tech to consistently and systematically scrub digital information the government deems inaccurate or worse, misinformation online.

Join The Conversation! | https://trialsitenews.com/ A major media member of the Trusted News Initiative (TNI) has warned a primary tech member about vaccine injury groups gaming the system to avoid algorithm detection and thus scrutiny. In what could be described as a dangerous move, the BBC collaborates with Facebook to shut down vaccine injury support groups by universally referring to them as “anti-vaccine” or “anti-vaxxers” and calling out the ways that they use carrot emojis to hide from Facebook their true identity.

In this must watch episode of Uncensored, Shabnam Palesa Mohamed engages in a riveting conversation with the incisive Dr Aaron Kheriaty, psychiatric physician, multi-platform writer, and author of The New Abnormal - The Rise of The Bio-Medical Security State. Dr Kheriaty Shares with Trialsite News the courageous motivation behind the court case launched by him together with Prof. Jay Bhattacharya and Dr Martin Kuldorff, in which they challenge being censored by social media tech giants about everything C19, but in particular vaccine injuries. Reveals the latest developments and shocking injury and death findings in the PHMPT court case against Pfizer, instituted for the release of clinical and safety data Pfizer tried to hide for 75 years. States that "science is incompatible with censorship", and calls those defending Big Pharma liability for vaccine injuries and so called 'sudden adult death syndrome' "sociopathic." Issues a bold statement against the World Health Organisation: Its proposed and dystopian global pandemic treaty is nothing but a "naked power grab", driven by rampant conflicts of interest. Talks about his new book The New Abnormal - The Rise of The Bio-Medical Security State, which analyses the dangers of vaccine IDs, state-corporate surveillance, the social credit system, and the World Economic Forum agenda. Pre-orders are open in October via Amazon.

Join The Conversation! | https://trialsitenews.com/ Litigation counsel for NCLA, Jenin Younes, speaks to TSN's Sonia Elijah on her landmark lawsuit against the federal government over online censorship Jenin Younes, civil liberties litigator for New Civil Liberties Alliance is representing four private plaintiffs: Jay Bhattacharya, Martin Kulldorff, Aaron Kheriaty and Jill Hines in what will probably be known as one of the most important lawsuits ever filed, when it comes to online censorship. Bhattacharya and Kulldorff, two of the co-authors of the Great Barrington Declaration, have come under intense fire by Big Tech censors. Shockingly, legal discovery has unveiled that the likes of Twitter and Facebook, acted under the direction of the Biden administration. The sprawling spread of federal-led censorship involves multiple government agencies, such as the CDC, DHS, HHS and the NIH. A recent victory in the court proceedings was won when the judge ordered discovery from both Anthony Fauci, director of NIAID and Chief Medical Advisor to President Biden and the White House's press secretary Karine Jean-Pierre.

Join The Conversation! | https://trialsitenews.com/ A petitioner in India’s Bombay High Court claims that the COVID-19 vaccine called Covishield killed his daughter and is now seeking compensation for the loss. The claimant argues that his daughter’s death is directly linked to the side effects of Covishield, the viral vector COVID-19 vaccine originally developed by University of Oxford, licensed by AstraZeneca for the Indian subcontinent and other parts of the world, then licensed for production and commercialization to the Serum Institute of India (SII), the world’s busiest vaccine producer. Originally labeled ChAdOx1 nCoV-19, or the Oxford/AstraZeneca vaccine, the U.S. Food and Drug Administration cancelled clinical trials in the U.S. earlier during the pandemic due to safety incidents. India’s drug regulator (Drug Controller General of India) granted emergency authorization for the product at the start of 2021 by SII. TrialSite reported that SII made moves last year lobby the government to remove all liability for these COVID-19 vaccines, much like is the case in the United States with the PREP Act. The claimant has served multiple parties from SII to the Bill Gates Foundation.

Weaponization of mRNA/DNA technology is an open question and a distinct possibility. DOD-Pharma contracts for vaccines specify this technology as dual-use, specifically having both "civilian and military applications". This presentation pulls together various sources of data and evidence. I discuss how these technologies can be weaponized, the mechanisms and possible impact. Let's start connecting the dots. The letter to Australian TGA and explanation of the FOIA request about miRNAs is here: https://covidmedicalnetwork.com/open-letters/open-letter-to-atagi.aspx

Join The Conversation! | https://trialsitenews.com/ The disaster that has been the U.S. Centers for Disease Control and Prevention (CDC), the Food and Drug Administration (FDA), and the National Institutes of Health (NIH) continues to unfold with fallout on all fronts and serious ramifications for the trio’s credibility moving forward. From the CDC acknowledging its bungled much of the pandemic response to high-profile departures in the FDA—due to a series of questionable high-profile decisions, such as authorizing the COVID-19 vaccines for babies as young as 6 months old—to proactive wars on doctors who prescribe generic repurposed drugs for COVID-19 and clear industry capture in at least parts of the NIH, TrialSite News has chronicled wild crony capitalism run amok, including regulatory capture throughout the pandemic at high levels of the U.S. Health and Human Services (HHS) as well as even the White House. Early on, few in the media, health care sector or government responded to TrialSite News articles chronicling these problems, but the desire to reform these badly hurt, one-time Gold Standard agencies, picks up momentum. Soon the pressure will build for serious reform.

Arcturus Therapeutics obtained a 63 million-dollar grant from the Biomedical Advanced Research and Development Authority (better known as the government program, BARDA). This will support the development of a self-amplifying mRNA vaccine for influenza. The award provides the funding over three years to support preclinical, manufacturing, nonclinical safety studies, along with development and regulatory support for Arcturus’ vaccine platform technology through Phase 1 clinical studies.

Join The Conversation! | https://trialsitenews.com/ Although small, not yet peer reviewed, and barely mentioned by any media when it first was uploaded to a preprint server three months ago, a National Institutes of Health (NIH)-sponsored observational study in the form of a clinical evaluation involved patients with new onset paresthesia’s (abnormal sensations often caused by pressure or damage to peripheral nerves) with or without autonomic symptoms incident to SARS-CoV-2 vaccination and response to immunotherapy with corticosteroids or intravenous immunoglobulin (IVI). This study was led by Principal Investigators affiliated with the National Institute of Neurological Disorders and Stroke, part of the National Institutes of Health, along with a group of respected neurologists employed with Thomas Jefferson University, Icahn School of Medicine at Mt. Sinai, Johns Hopkins University School of Medicine, and Massachusetts General Hospital (Department of Neurology and Pathology/Neuropathology).

Join The Conversation! | https://trialsitenews.com/ The Founder of Trial Site News speaks candidly about the need for transparent clinical research information, the rise of unprecedented censorship & how Trial Site News is fighting back against the Trusted News Initiative TrialSite News Crowdfunding Link | https://www.picmiicrowdfunding.com/deal/TrialSite%20News/

Windtree Therapeutics is advancing multiple late-stage interventions for acute cardiovascular and pulmonary syndromes to support patients. Their goal is to develop unique therapies that significantly improve upon the treatment of severe, acute conditions such as heart failure and lung injury.

We discuss the history of seasonal flu vaccines, how the CDC and FDA make decisions on selecting the new strains each season, the failures of the 1976 and 2009 swine flu vaccine campaigns, and ponder how the CDC and FDA make a giant leap to novel mRNA/DNA technologies and absolve them of any clinical trials requirements, without any relevant laws amended by the US Congress.

In this episode of Lawctivist with Shabnam Palesa Mohamed, attorney Bobbie Ann Cox and advocate Sabelo Sibanda share explosive information and parallels about attempts by both New York State and the South African Government to enforce testing, treatments, isolation and quarantine camps. In both situations, the law is being used to achieve dystopian socio-economic agendas. The call to action is for international solidarity to take power back and to restore informed consent and inalienable human rights.

Mike Totterman is a successful entrepreneur in medical devices, pharmaceutical clinical trials and commercialization of academic inventions in several fields of medicine. He explains the process of due diligence as it is applied by early stage investors to the evaluation of new technologies in medicine, understanding the risks, evaluation of scalability and reliability in manufacturing. We look at Moderna investor presentation from 2018 as an example of lack of disclosure or due diligence.

Join The Conversation! | https://trialsitenews.com/ Dr. Ron Brown has written over a dozen research articles published on Pub Med investigating novel causes of diseases and their prevention through dietary modification. Dr. Brown's research articles are available on his Google Scholar profile, under Ronald B. Brown.

We discuss the history of seasonal flu vaccines, how the CDC and FDA make decisions on selecting the new strains each season, the failures of the 1976 and 2009 swine flu vaccine campaigns, and ponder how the CDC and FDA make a giant leap to novel mRNA/DNA technologies and absolve them of any clinical trials requirements, without any relevant laws amended by the US Congress.

This financing is to accelerate the development of new therapies to treat severe blood cancers and solid tumors, including further clinical development of the flagship project RVU120. RVU120 is a selective CDK8 kinase inhibitor in clinical development for the treatment of acute myeloid leukemia and high-risk myelodysplastic syndromes, as well as solid tumors.

Join The Conversation! | https://trialsitenews.com/ Dr. Denise Faustman, MD, PhD heads the Faustman Lab, an Immunobiology Laboratory at the Massachusetts General Hospital, affiliated with Harvard Medical School. Her focus is on understanding the role the immune system plays in autoimmune diseases, cancer and transplantation. Her most recent research discussed in this podcast is titled "Multiple BCG vaccinations for prevention of COVID-19 and Other Infectious Diseases in Type 1 Diabetes" and published in Cell Reports Medicine. Link | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376308/ Faustman Lab | https://www.faustmanlab.org/