The leading developer of vaccines and therapeutics for coronavirus disease, Pfizer (NYSE: PFE), is to build new facilities in France as part of a near-$600 million investment in production of Paxlovid (nirmatrelvir/ritonavir).
While the antiviral is not approved in the European Union, it has been authorized for emergency use, and the European Medicines Agency is currently reviewing an application for conditional marketing approval.
The USA and the UK have both approved the treatment, which is a combination of two pills, for people who are at risk of developing severe disease.
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