The US Food and Drug Administration has weighed in on the question of coronavirus vaccine dosing, as health experts and the general public alike discuss the best way to optimize limited supplies.
Two innovative mRNA-based vaccines for COVID-19 disease have been approved by regulators, including in the USA, and both require two doses, given several weeks apart.
In the UK, public health authorities have taken the unusual step of recommending that doctors deviate from the dosing schedule which was shown to be safe and effective in Phase III trials.
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 accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
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
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze