BOOM, small victory but one nonetheless as Trump's RFK Jr. (Robert Kennedy Jr.) stops (pauses) METHODOLOGICALLY flawed Vaxart oral COVID tablet DNA vectored vaccine trial involving 10,000 subjects;
"Kennedy Jr. suspended the Biden administration's multimillion-dollar contract to create a new COVID-19 vaccine...IMO, major methodological flaws with the Vaxart study that warrants it be terminated!
Excellent move by Kennedy Jr.!
Why? Because
1)the Vaxart research methods appear very sub-optimal
2)the methods are not clearly outlined for a proper track of steps for oversight
3)the trial arms seek to compare the oral COVID tablet to an active existing comparator (mRNA vaccine) and not against placebo which is optimal to assess if it works e.g. ‘Vaxart, Inc. (Nasdaq: VXRT) today announced completion of enrollment of the sentinel cohort of a Phase 2b clinical trial evaluating Vaxart’s oral pill COVID-19 vaccine candidate against an approved mRNA vaccine comparator. The sentinel cohort comprised of 400 participants, with 200 receiving Vaxart’s COVID-19 vaccine candidate and 200 receiving an approved mRNA vaccine comparator.’
4)a classical vaccine can never be produced via use of mRNA or DNA, this has always been a lie
5)using antibody titers, surges in vaccine-induced antibodies is worthless as a measure of efficacy or effectiveness; we need hard objective patient-important outcomes like death, severity, hospitalization; immuno-bridging is not a proper method
6) the baseline risk today for COVID or whatever this was, is basically ZERO…near none exists in the population…that means that once randomized, it will be impossible to randomize cases that could benefit (or even be harmed) by the agents under study for there is no pathogen circulating at levels to even be detected or to eve have an effect for the then agents to work. If the baseline risk is ZERO in the population of the illness, then how would you be able to detect MEANINGFUL differences between the two comparative arms? It is a useless study. It will find nothing, and the results will be NO difference. Again, you cannot get meaningful results if the comparator is an active vaccine. This again makes this methodologically flawed.
7)All of the COVID injections end in the spike protein that is a deadly toxic molecule e.g. endothelial pathogen, highly inflammatory, excessive auto-immunity risk and trajectory, immune attack on cells via cytotoxic, cytolytic immune cells, on cells that make the spike protein from injected mRNA (packaged in the LNP transport vessel) and express it on its surface, damages the immune system e.g. Toll-like receptors 7, 8, subverts the P53 tumor suppressor gene guardian of the genome, and whether the Malone Bourla Bancel et al. mRNA-LNP platform or the DNA viral vector platform e.g. may deliver DNA for spike protein that is then transcribed to mRNA then to protein synthesis etc. All result in the spike protein as part of the immune response, that is deadly.
Great move by Kennedy Jr.!
"While it is crucial that the Department [of] Health and Human Services (HHS) support pandemic preparedness, four years of the Biden administration’s failed oversight have made it necessary to review agreements for vaccine production, including Vaxart’s," Kennedy said in comments provided to Fox News Digital on Tuesday.
‘Kennedy issued a 90-day stop-work order on Friday related to the HHS contract with American biotech company Vaxart Inc., which is working to develop a new COVID-19 vaccine that can be taken orally. The stop-work order comes as 10,000 individuals were slated to begin clinical trials on Monday.’
‘Kennedy and other health officials set to examine the study's initial findings over the next 90 days before deciding on next steps.’
The creation of a new COVID-19 vaccine was part of the Biden administration's $4.7 billion Project NextGen initiative, which was launched in 2023 and works to streamline the development of new vaccines. The Vaxart vaccine was specifically funded through an agreement with the Biomedical Advanced Research and Development Authority (BARDA), which is a department within the Administration for Strategic Preparedness and Response under the HHS umbrella.’
HHS pauses $240 million Biden-era project to create new COVID vax | Fox News
A recent modification to the contract would have allowed Vaxart to invoice BARDA for the remaining roughly $230 million for clinical trials (240 of ~460 already obligated), but the stop-work order prevents the biotech company from invoicing BARDA until further notice. Vaxart, however, can still invoice HHS related to medical monitoring of individuals who took part in an initial round of trials, Fox Digital learned.’
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you cannot run a study like this when the baseline population risk is zero...how could you detect a difference less than zero? you would need to randomized the entire US population and still will not detect a difference. this study is bull shit, methodologically impossible, this is just grift
Now halt the rest! DO IT! I know someone who works in organ transplant and MANY donors have flu and have had flu shots or the combo flu and CV and whatever-else-they-can-stick-in-them shots. It’s all a FRAUD!