Novavax COVID-19 vaccine submitted for regulatory approval to Health Canada
Global News
The Novavax COVID-19 vaccine is the first protein-based vaccine candidate of its kind.
Another COVID-19 vaccine could soon be on the market as Novavax has officially filed for regulatory approval of its vaccine to Health Canada.
The Novavax COVID-19 vaccine is the first protein-based vaccine candidate of its kind. The vaccine was created using recombinant nanoparticulate technology from the first strain of SARS-Cov-2.
“Novavax continues to deliver regulatory filings that we expect will bring the first protein-based COVID-19 vaccine based on Phase 3 data to the world,” said Stanley C. Erck, president and chief executive of Novavax in a press release. “We thank the Government of Canada and the European Commission for their ongoing partnership and confidence in our COVID-19 vaccine program.”
Novavax has released data from vaccine trials conducted in June 2021 in U.S. and Mexico. With 30,000 participants in the trials, the U.S.-based company saw a 100 per cent protection against moderate and severe cases of COVID-19 with an overall efficacy of 90.4 per cent. Earlier trials in the U.K. saw the efficiency of the vaccine at 89.3 per cent.
In June, Novavax wrote that it was prepared to be “on track to reach manufacturing capacity of 100 million doses per month by the end of the third quarter and 150 million doses per month by the end of the fourth quarter of 2021,” if it received regulatory approval.
A spokesperson for the company said the submission to Canadian health authorities comes as Novavax received recent approval for use in Indonesia. It also intends to follow up and do a “completion of data submission in the European Union.” The company has been busy across the globe with another provisional approval application made for the vaccine in Australia on Oct. 30.
The vaccine manufacturer said it plans to deliver COVID-19 vaccines to developing countries and is committed to the COVAX program, a global initiative aimed at increasing global vaccine accessibility.
“The approval and submissions this week — bring us closer to helping fill these important global needs,” wrote a spokesperson in an email.
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