More real-world safety data, especially in patients with a high risk of cardiovascular disease, could potentially address the issue of under-dosing and under-treatment with novel oral anticoagulants (NOACs) in global practice, says an analyst.
According to Dr Lakshmi Dharmarajan, research and consulting firm GlobalData's senior analyst covering cardiovascular and metabolic disorders, while the underutilization of NOACs is a commonly acknowledged issue due to the approved lower doses of these drugs in the US, this could change with the launch of new NOAC antidotes in the near future.
Antidotes under development
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