Novavax COVID-19 vaccine receives backing from European Medicines Agency
The European Medicines Agency has backed the Nuvaxovid COVID-19 vaccine for adults as a booster shot to other COVID-19 vaccines.
Novavax’s COVID-19 vaccine, Nuvaxovid, has been backed by the European Medicines Agency for use as a booster shot for adults ahead of the winter season.
Nuvaxovid, designed to target the original viral strain that emerged in Wuhan, China in December 2019, is being recommended by the EMA for individuals who had been previously inoculated with either Nuvaxovid or another COVID-19 vaccine. Though developed and debuted long after the mRNA vaccines, the Novavax vaccine was developed with the hope that individuals skeptical of the newer mRNA technology would be incentivized to get vaccinated with more familiar technologies.
The EMA’s recommendation of Nuvaxovid comes on the heels of their backing of two separate COVID-19 vaccine boosters designed to target the Omicron variant of SARS-CoV-2. The bivalent shots, targeting both the BA.1 Omicron variant and the original viral strain, were developed by Moderna and the Pfizer/BioNTech teams.
Though uptake of Nuvaxovid has been tepid in the United States, where the vaccine has been available since February of this year, the hope is that it may still offer a booster option for those who have previously received other vaccines, broadening the spectrum of potential COVID-19 protection.
Source: EU regulator backs use of Novavax COVID shot as a booster | Reuters
Related News
-
News Swiss pharma industry warns US tariffs could harm global patient care
The Swiss pharmaceutical sector has raised alarms over new US tariffs on medicines, warning of disrupted supply chains, increased costs, and delayed innovation, all of which could jeopardise patient access to essential treatments worldwide.
-
News Women in Pharma: CPHI India – India’s Pharmaceutical Industry and Gender Inclusion Challenges
India’s pharmaceutical industry has emerged as a significant player in the global market, valued at USD 50 billion in FY 2023-2024, according to Frost & Sullivan’s analysis. This sector encompasses a diverse portfolio, including drugs, vacc... -
News Biogen acquires Apellis Pharmaceuticals to boost immunology and rare disease profile
Biogen Inc. has announced its acquisition of Apellis Pharmaceuticals, Inc., a move that is set to significantly enhance its growth portfolio in immunology and rare diseases. The agreement, valued at approximately US$5.6 billion, will see Biogen purchas... -
News Gilead Sciences acquires Ouro Medicines for over US$2 billion
Gilead Sciences confirms a deal to take over Ouro Medicines, adding to a portfolio of therapies for autoimmune diseases.
-
News Women in Pharma: Advancing Women's Health
Discover the latest innovations in technologies and therapeutics that are revolutionising women's health in our latest CPHI Online Women in Pharma infographic.
-
News CPHI Pharma Awards 2026: Recognising Excellence in an Evolving Industry
Submissions now open — deadline May 16
-
News Dr Reddy's to launch generic semaglutide in India
Dr Reddy’s Laboratories, one of India’s leading pharmaceutical companies, is preparing to launch a generic version of semaglutide, branded as Obeda, in March. Obeda is expected to provide a more affordable alternative to Ozempic a... -
News Frontier Biotech and GSK Forge RNA Therapy Partnership
Frontier Biotechnologies and GSK have entered a global licensing agreement to advance small interfering RNA (siRNA) therapeutics. This collaboration grants GSK exclusive rights to develop and commercialise two promising siRNA candidates, marking a mile...