Novavax Inc.,confirms European Medicines Agency review of COVID-19 vaccine, Nuvaxovid, filed for conditional marketing authorization.
The company announced earlier this month that it had completed the submission of all data and modules required by EMA for regulatory evaluation of NVX-CoV2373, Novavax' recombinant nanoparticle protein-based COVID-19 vaccine with Matrix-M adjuvant. EMA has indicated that its assessment will proceed under an accelerated timeline, with an opinion issued potentially within weeks.
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