COVID-19 VACCINE LETHAL INJECTIONS

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Novavax
COVID-19 Vaccine

(Novavax, USA)

The Official Story

NOVAVAX COVID-19 VACCINE
(Novavax, USA)

The Novavax COVID-19 vaccine, sold under the brand names Nuvaxovid and Covovax, among others, is a subunit COVID-19 vaccine developed by Novavax and the Coalition for Epidemic Preparedness Innovations (CEPI). Full results from Nuvaxovid’s pivotal phase III trial were published in December 2021.

Technology

NVX-CoV2373 has been described as both a protein subunit vaccine and a virus-like particle vaccine, though the producers call it a “recombinant nanoparticle vaccine”.

The vaccine is produced by creating an engineered baculovirus containing a gene for a modified SARS-CoV-2 spike protein. The spike protein was modified by incorporating two proline amino acids in order to stabilize the pre-fusion form of the protein; this same 2P modification is being used in several other COVID 19 vaccines. The baculovirus is made to infect a culture of Sf9 moth cells, which then create the spike protein and display it on their cell membranes. The spike proteins are harvested and assembled onto a synthetic lipid nanoparticle about 50 nanometers across, each displaying up to 14 spike proteins.

The formulation includes a saponin-based adjuvant named Matrix-M.

Legal status

In February 2021, the European Medicines Agency (EMA) started a rolling review of the Novavax COVID-19 vaccine (NVX CoV2373). In November 2021, the EMA received application for conditional marketing authorization. On 20 December 2021, the European Commission granted a conditional marketing authorization across the EU, following a recommendation from the European Medicines Agency (EMA), for it to be sold under the brand name Nuvaxovid.

As of November 2021, it has been authorized for use in Indonesia, the Philippines, as of December in India, as of January 2022 in South Korea, Australia, as of February 2022 in the United Kingdom, Canada, Taiwan, and Singapore. As of December 2021 it was validated by the World Health Organization.

On 3 June 2022, the FDA’s advisory committee voted 21-0 with one abstention to recommend authorization of Novavax’s vaccine for use in adults in the United States. On 13 July 2022, the FDA authorized NVX-CoV2373 for emergency use as a primary immunization (not booster) in adults. making it the fourth COVID 19 vaccine authorized in the US. On 19 July 2022, the US Centers for Disease Control and Prevention (CDC) recommended the Novavax COVID 19 vaccine as a two-dose primary series for adults age 18 and older, thus endorsing the recommendation from the Advisory Committee on Immunization Practices (ACIP) regarding this vaccine. On 19 August 2022, the FDA granted Emergency Use Authorization for the Novavax COVID 19 vaccine in people aged 12-17 years. On 22 August 2022, the CDC recommended the Novavax COVID 19 vaccine for adolescents aged 12-17 years.

Source: Wikipedia

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Novavax COVID-19 Vaccine

The Novavax COVID-19 vaccine, codenamed NVX-CoV2373, is a subunit COVID-19 vaccine candidate developed by Novavax and the Coalition for Epidemic Preparedness Innovations, that is undergoing trials in India under the brand name Covovax. It requires two doses and is stable at 2 to 8 °C (36 to 46 °F) refrigerated temperatures.

NVX-CoV2373 has been described as both a protein subunit vaccine and a virus-like particle vaccine, though the producers call it a “recombinant nanoparticle vaccine”.

Novavax Worldwide Authorizations

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