Friday, October 23, 2026
WA
Home NorthEast Caravan Health & Lifestyle WHO lists 10th COVID-19 vaccine for emergency use: Nuvaxovid

WHO lists 10th COVID-19 vaccine for emergency use: Nuvaxovid

0
855
Vaccine
Vaccine

WHO lists 10th COVID-19 vaccine for emergency use: Nuvaxovid

21 December 2021 – Geneva, Switzerland – The World Health Organization issued an emergency use listing (EUL) for Nuvaxovid™, following its assessment and approval by the European Medicines Agency (EMA) earlier today.

The new vaccine was developed by Novavax and the Coalition for Epidemic Preparedness Innovations (CEPI), and is the originator product for the Covovax™ vaccine that received WHO emergency use listing on 17 December.

Both vaccines are made using the same technologies. They require two doses and are stable at 2 to 8 °C refrigerated temperatures.

WHO’s Strategic Advisory Group of Experts on Immunization has also issued policy recommendations for Nuvaxovid™ / Covovax™.

WHO emergency use listing

The emergency use listing (EUL) procedure assesses the suitability of novel health products during public health emergencies. The objective is to make medicines, vaccines and diagnostics available as rapidly as possible to address the emergency while adhering to stringent criteria of safety, efficacy and quality. The assessment weighs the threat posed by the emergency as well as the benefit that would accrue from the use of the product against any potential risks.

The EUL pathway involves a rigorous assessment of late phase II and phase III clinical trial data, as well as substantial additional data on safety, efficacy, quality and a risk management plan. These data are reviewed by independent experts and WHO teams who consider the current body of evidence on the vaccine under consideration, the plans for monitoring its use, and plans for further studies.

As part of the EUL process, the company producing the vaccine must commit to continue to generate data to enable full licensure and WHO prequalification of the vaccine. The WHO prequalification process will assess additional clinical data generated from vaccine trials and deployment on a rolling basis to ensure the vaccine meets the necessary standards of quality, safety and efficacy for broader availability.

LEAVE A REPLY

Please enter your comment!
Please enter your name here

Adblocker detected! Please consider reading this notice.

We've detected that you are using AdBlock Plus or some other adblocking software which is preventing the page from fully loading.

We don't have any banner, Flash, animation, obnoxious sound, or popup ad. We do not implement these annoying types of ads!

We need money to operate the site, and almost all of it comes from our online advertising.

Please add https://www.ibgnews.com to your ad blocking whitelist or disable your adblocking software.

×
Verified by MonsterInsights