German life sciences group Bayer (BAYN: DE) had a welcome opportunity on Friday to talk about some news that did not involve potential problems with its takeover of the US agro-chemicals company Monsanto.
The group’s pharma unit was able to boast that the European Commission had approved a new indication of the non-vitamin K antagonist oral anticoagulant Xarelto (rivaroxaban).
A 2.5mg twice-daily regimen has been approved, to be taken with acetylsalicylic acid once a day, for the prevention of atherothrombotic events in adult patients with coronary artery disease (CAD) or symptomatic peripheral artery disease (PAD) at high risk for ischemic events.
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