Italian Medicines Agency Agenzia Italiana del Farmaco

EMA recommends Nuvaxovid for authorisation in the EU - EMA recommends Nuvaxovid for authorisation in the EU

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EMA recommends Nuvaxovid for authorisation in the EU

EMA has recommended granting a conditional marketing authorisation for Novavax’s COVID-19 vaccine Nuvaxovid (also known as NVX-CoV2373) to prevent COVID-19 in people from 18 years of age.

Nuvaxovid is the fifth vaccine recommended in the EU for preventing COVID-19. It is a protein-based vaccine and, together with the already authorised vaccines, will support vaccination campaigns in EU Member States during a crucial phase of the pandemic.

After a thorough evaluation, EMA’s human medicines committee (CHMP) concluded by consensus that the data on the vaccine were robust and met the EU criteria for efficacy, safety and quality.


Published on: 23 December 2021

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