The Commission has authorised the Nuvaxovid XBB.1.5-adapted COVID-19 vaccine, developed by Novavax. This is another important step in the fight against the disease. It is the first protein-based adapted vaccine authorised for this autumn and winter season.
The European Medicines Agency (EMA) carried out an in-depth evaluation of the vaccine. Following this evaluation, the Commission authorised the adapted vaccine under an expedited procedure so that Member States have sufficient time to prepare for their autumn-winter vaccination campaigns.
In line with previous recommendations by the EMA and the European Centre for Disease Prevention and Control (ECDC), adults and adolescents from 12 years of age who require vaccination are invited to get a single dose, irrespective of their COVID-19 vaccination history.
Commission approves new contract for a potential COVID-19 vaccine with Novavax |
Background
With the EU Vaccines Strategy, the Commission continues to ensure that Member States have access to the latest authorised COVID-19 vaccines to protect the vulnerable members of their population and deal with the epidemiological evolution of the virus.
Novavax has adapted its COVID-19 vaccine to target the SARS-CoV-2 Omicron strain XBB.1.5. This is in line with ECDC-EMA statement on updating COVID-19 vaccines composition for new SARS-CoV-2 variants. The adapted vaccine is also expected to increase the breadth of immunity against current dominant and emerging variants.
More information: European Commission
Publicaciones relacionadas:
Global regulators discuss data requirements for phase 3 trials of COVID-19 vaccines
European Commission unveils EU vaccines strategy
First COVID-19 treatment recommended for EU authorization
Commission lists key steps for effective vaccination strategies and vaccines deployment
Commission approves contract with Moderna to ensure access to a potential vaccine
Leave a Reply