Biotechnology company Novavax announced that it has made a modification to an existing contract with the U.S. Department of Health and Human Services (HHS) and the Department of Defense (DoD) to provide up to 1.5 million more doses of its Nuvaxovid COVID-19 vaccine (also known as “NVX-CoV2373” and “Covovax”), in addition to the 3.2 million doses of the shot sold to the government last year.
The modification stipulates that the government will increase public access to the vaccine and support the development of smaller dose vials, strain selection consistent with recommendations by the Food and Drug Administration (FDA), and an orderly transition for distribution to the commercial market.1
John C. Jacobs, president and CEO of Novavax, said:
This agreement acknowledges the need to offer the American people a diverse COVID-19 vaccine portfolio and underscores the importance of Novavax’ partnership with the U.S. government to ensure continuous access to a protein-based option as part of public health measures.2
Nuvaxovid has not been officially licensed by the FDA, but has been granted Emergency Use Authorization (EUA) by the agency for distribution to individuals 12 years of age and older.3
Nuvaxovid is a protein subunit COVID vaccine containing the SARS-CoV-2 spike protein and an adjuvant known as Matrix-M composed of saponin extracts, phospholipids and cholesterol, which is designed to trigger a very strong immune response.4 The spike protein in this vaccine is produced in baculovirus insect cells. The Matrix M-adjuvant contains saponin extracts from the bark of the Soapbark tree that is native to Chile.5 6
U.S. Public Health Officials Hope Novavax’s Vaccine Will Appeal to Americans Worried About mRNA Shots
The U.S. Centers for Disease Control and Prevention (CDC) conducted an opt-in Internet survey of 1,200 COVID–vaccinated adults to assess the reasons for receiving or not receiving Pfizer/BioNTech’s Comirnaty messenger RNA (mRNA) bivalent COVID booster shot. The results showed that 22.7 percent of respondents said that they had chosen not to get the mRNA booster due to concerns about adverse reactions. This concern was more prevalent among those who were over 60 years old.7
Guy Palmer, PhD, a professor of pathology and infectious diseases at Washington State University, said he believed that Nuvaxovid could appeal to Americans who are concerned about the safety of mRNA shots. “There’s a slight open door there for a non-mRNA vaccine like Novavax.” Dr. Palmer said.
Robert Schooley, MD, an infectious disease specialist at UC San Diego Health, noted:
Novavax essentially uses the same approach as mRNA vaccines, but they make the protein in a factory. So they’re giving you the protein itself, rather than instructions for your cells to make a protein.8
The Nuxaxovid vaccine has been shown to cause severe adverse reactions in Phase 1 part of a Phase 1/2 human clinical trials.9 Cases of myocarditis (inflammation of the heart muscle) or pericarditis (inflammation of the membrane around the heart) were detected in Novavax clinical trials.10
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Click here to view References:1 Novavax. U.S. Government and Novavax Extend Partnership, Securing Up to 1.5 Million Additional Doses of Novavax’ COVID-19 Vaccine. Feb. 13, 2023.
2 Ibid.
3 Ibid.
4 U.S. Centers for Disease Control and Prevention. Understanding How COVID-19 Vaccines Work. Feb. 3, 2023.
5 Creative Biolabs. Saponin.
6 U.S Food and Drug and Administration. Novavax COVID-19 Vaccine, Adjuvanted. Oct. 31, 2022.
7 Sinclair A et al. Reasons for Receiving or Not Receiving Bivalent COVID-19 Booster Vaccinations Among Adults — United States, November 1–December 10, 2022. The Morbidity and Mortality Weekly Report 2023; 72(3): 73–75.
8 Constantino AK. Novavax’s new Covid vaccine is perfect for people scared of mRNA tech—but it won’t win over the unvaccinated. CNBC Jul. 15, 2022.
9 Cáceres M. Novavax’s Adjuvanted COVID-19 Vaccine Caused Severe Adverse Reactions in Clinical Trials. The Vaccine Reaction Sept. 14, 2020.
10 Twentyman E et al. Interim Recommendation of the Advisory Committee on Immunization Practices for Use of the Novavax COVID-19 Vaccine in Persons Aged ≥18 years — United States, July 2022. The Morbidity and Mortality Weekly Report 2022: 71(31): 988–992.
8 Responses
I thought the Emergency is over and US won’t $ any more COVID ?.
The delivery system is the problem. A soup of chemicals, metal particles, adjuvants, foreign animal proteins, preservatives….injected straight into your bloodstream. You are putting toxins in a person’s body and expecting health? No one, to date, has shown the existence of the alleged covid19 virus. No one has isolated the alleged virus. You can’t make a vaccine for something you have no sample of.
They are shooting in the dark.
Just like but in new born babies and toddlers for their shots!! Compared to an adult.
The government can take those 1.5 million doses of clot shots and shove them where the sun don’t shine.
The problem isn’t the delivery system but rather the malicious intent of the mad scientists that are behind all that is c 19. c 19 is the trojan horse upon which all the authoritarianism and depopulation you can image rides to victory.
Feb 18, 2023 NEWS: 132 Canadian doctors have died suddenly or unexpectedly since COVID-19 vaccine rollout (Part 2/2)
Overall Canadian physician mortality in 2022 was 53% higher than 2019, however, as with all excess mortality data in highly COVID-19 vaccinated jurisdictions, this mortality is heavily skewed towards the younger age groups, with the youngest doctors – medical students or medical residents under age 30 dying at a 900% higher rate in 2022, compared to the 2019/2020 average.
https://makismd.substack.com/p/news-132-canadian-doctors-have-died-38e?utm_source=post-email-title&publication_id=1385328&post_id=103722804&isFreemail=true&utm_medium=email
https://substackcdn.com/image/fetch/f_auto,q_auto:good,fl_progressive:steep/https%3A%2F%2Fsubstack-post-media.s3.amazonaws.com%2Fpublic%2Fimages%2F2e3a0bb0-ad1c-4527-8750-e196c4779e41_1099x1111.jpeg
“Nanotechweapon” is the CORRECT TERM IN REFERENCE to the “AI Nanotechweapon” the DOD catagorized a ‘Countermeasure’ and the FDA, HHS, CDC, NIAID and other TREASONOUS Alphabet Minions defined ‘Vaccines’ after the word ‘Vaccine’ was REDEFINED TO INCLUDE INNOCUOUS LANGUAGE ALLOWING THIS POISONOUS SERUM TO BE DEFINED AS IT WAS.
Dr. Astrid Stuckelberger spoke at the Lakaruppropret in Stockholm, Sweden about Graphene Oxide being an ingredient inside these vials of serum which DO NOT CONTAIN Nitrogen or Phosphore WHICH MEANS THEY ARE NOT BIOLOGICAL. These serums; however do contain all kinds of metals and this includes SELF-ASSEMBLING NANOPARTICLES THAT BECOME BLUE TOOTH TECHNOLOGY which emits EMF RADIATION Signals allowing human beings to be SURVEILLED WHICH ITSELF IS POISONOUS.
STOP REFERENCING THESE “Nanotechweapons” as Vaccines WHEN THEY ARE NOT. About time we speak ACCURATELY AND CONCISELY TO FIX THE TYRANNY OF THE Globalist Death CULT’S POWER GRAB. TIME to indict, try and PUNISH PUBLICALY TO THE POINT THAT THESE CRIMINALS AGAINST HUMANITY torturing, enslaving and genociding the world’s population they define their ‘Human Herd’ throughout all time at will never happens again.