US FDA questions wisdom of relaxed vaccine dosing schedule

5 January 2021
lab_biotech_research_vaccine_big

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 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