Given that the task of tackling the coronavirus pandemic is arguably the biggest – and certainly the highest profile – challenge that the pharmaceutical industry has faced this century, it is appropriate that the world’s largest pharma company is among the leaders of the race to find a vaccine.
Pfizer (NYSE: PFE) and Germany’s BioNTech (Nasdaq: BNTX) could file for US emergency use approval of their two-dose COVID-19 vaccine, known as BNT162b2, later this month.
Clinical data on BNT162b2 is currently being submitted to other regulatory agencies, including the European Medicines Agency and Health Canada, under a ‘rolling review’ procedure which is intended to speed up the process.
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