Still playing catch-up, Novavax gains booster nod in USA

20 October 2022
vaccine_shot_jab_booster_big

An alternative to mRNA-based coronavirus vaccines has received an Emergency Use Authorization (EUA) in the USA, providing a new option for a first booster dose.

Developed by US biotech Novavax (Nasdaq: NVAX) and marketed elsewhere as Nuvaxovid, the recombinant, adjuvanted jab has been created using a more traditional vaccine technology.

While rates of vaccination are high in the USA, interest in booster jabs has waned as the first waves of the pandemic recede. Novavax may hope to access part of the market which is skeptical about newer, mRNA-based vaccine technologies.

This article is accessible to registered users, to continue reading please register for free.  A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.

Login to your account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed

Chairman, Sanofi Aventis UK

Companies featured in this story

More ones to watch >


Today's issue

Company Spotlight





More Features in Biotechnology