Novavax COVID-19 vaccine shows 90.4% efficacy in late stage trial

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Novavax Inc said on Monday its COVID-19 vaccine candidate showed 90.4% overall efficacy against the disease in a late-stage trial.

The American biotechnology company Novavax announced on Monday that its coronavirus vaccine candidate was found to have an overall efficacy of 90.4% in a Phase 3 trial conducted across the United States and Mexico.

Additional analyses of the trial are ongoing, according to the company, and will be submitted to peer-reviewed journals for publication.

The trial results appear consistent with the efficacy and safety profile the vaccine previously showed in a Phase 3 trial conducted in the United Kingdom, Dr. Gregory Glenn, president of research and development for Novavax, told CNN.

“Different continent, different population, different viruses floating around, and yet, we still see really good efficacy,” Glenn said. “This is what you want to have.”

The study launched in December and enrolled 29,960 adults across 113 sites in the United States and six sites in Mexico. Some of the participants were given a placebo and some were administered two doses of the Novavax vaccine 21 days apart.

The company said the vaccine was “generally well-tolerated” and common side effects included pain at the injection site, lasting less than three days, and fatigue, headache and muscle pain, lasting less than two days.

Novavax’s coronavirus vaccine, called NVX-CoV2373, differs from the three vaccines already in use in the United States. The vaccine relies on what is called recombinant nanoparticle technology and Novavax’s adjuvant, called Matrix-M, to stimulate an immune response.

The two mRNA vaccines that were authorized last year in the United States — from Pfizer/BioNTech and Moderna — both use genetic material to stimulate an immune response. Johnson & Johnson’s single-shot vaccine, which was authorized in February, uses a weakened common cold virus as a vector to carry the genetic instructions.

Novavax said on Monday it plans to apply in the US for emergency use authorization of its vaccine in the third quarter of this year and is “on track” to manufacture about 100 million doses per month by the end of the third quarter.