The US Food and Drug Administration’s (FDA) approval of Seqirus’ cell-based influenza vaccine manufacturing process at a US facility will allow the company to more than double production levels of Flucelvax Quadrivalent.
Seqirus, the second-largest vaccine company in the world and part of Australia’s CSL Limited (ASX: CSL), will be able to dramatically ramp up production for supply in the 2019/20 influenza season.
The announcement is the latest step forward for Seqirus, which has delivered on its pledge to reach profitability within just three years of being set up. The cell-based technology was acquired from Swiss pharma giant Novartis (NOVN: VX) in 2015.
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