Sanofi, GSK Seek FDA Clearance for New Vaccine Offering Strong Protection Against Severe Infection

Sanofi and GlaxoSmithKline (GSK) are releasing a new COVID-19 vaccine, which looks to be one of the most successful vaccinations yet.

The vaccination shot developed by pharmaceutical companies in France and the United Kingdom is now seeking FDA clearance for its vaccine, which aims to better protect against severe diseases.

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A lab technician dedicated to the vaccines formulation, wearing Personal Protective Equipment (PPE), prepares stainless steel tanks for manufacturing vaccines preparations before the syringe filling phase, at a French pharmaceutical company Sanofi's world distribution centre in Val-de-Reuil on July 10, 2020. JOEL SAGET/AFP via Getty Images

Sanofi and GSK Bring Their Best COVID-19 Vaccine Shot for Approval

Sanofi stated in a statement that its vaccine has so far applied for approval to European health regulations and committees after completing its testing phase.

The French pharmaceutical business collaborated with GSK of the United Kingdom with the vaccination shot.

After a rigorous testing process and stage, the companies are ready to present their injections to the general public.

Sanofi and GSK further pointed out in a document that their vaccine has 100%* efficacy against the virus's severe illnesses, but that efficacy diminishes as the case worsens.

For moderate instances of COVID-19, the shot provides 75 percent protection, and for symptomatic or light cases, it provides 57.9% protection.

Along with the vaccine doses, a booster from Sanofi and GSK will be available to the public.

Previous vaccines concentrated on the original COVID-19 version, which was the source of all of the world's ills.

The new vaccine, on the other hand, is designed to combat severe infections caused by the coronavirus and has a different focus for people who will receive the shot.

Nonetheless, European officials questioned the Sanofi and GSK vaccine's distribution and availability.

COVID-19 Vaccine from Sanofi-GSK Might Lag For Symptomatic Case

While the Sanofi-GSK treatment appears to be on pace with mRNA shots to prevent severe disease and hospitalization, Sam Fazeli, a Bloomberg Intelligence analyst said the COVID-19 vaccine from the said pharmaceutical company may lag in terms of symptomatic case.

"The vaccine will find a place among people reticent to take mRNA vaccines and in lower-income countries, making for a modest commercial impact on Sanofi and Glaxo," Fazeli said per Live Mint.

COVID-19 vaccinations have already been provided in over 10 billion doses worldwide, indicating that demand increases from poorer countries and booster programs.

Sanofi-inoculation Glaxo's may have some advantages over other Covid vaccines. It can be stored and transported at refrigerator temperatures, making it more convenient than existing mRNA shots.

The product also uses Sanofi's recombinant protein technology for flu vaccinations and a Glaxo adjuvant to boost immune response.

However, Sanofi and Glaxo are now up against a new set of competitors with Covid injections. For example, Novavax Inc. has had a recombinant-protein product that the European Medicines Agency and the World Health Organization authorized since December.

After erroneously giving participants in an early-stage trial smaller doses than expected, Sanofi and Glaxo's candidate was delayed for months.

Check out more news and information on COVID-19 in Science Times.

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