With stocks reeling over safety concerns for blindness medicine Beovu (brolucizumab), Swiss pharma giant Novartis (NOV: NX) has begun an external review into the product.
Shares have fallen an astonishing 9% since the American Society of Retinal Specialists (ASRS) issued a communication to its members that could alter the risk/benefit profile for the macular degeneration drug.
Intended as a replacement for aging blockbuster Lucentis (ranibizumab), Novartis won approval from the US Food and Drug Administration in October 2019 and in Europe in February 2020.
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