Novo Nordisk’s (NOV: N) once-weekly drug Ozempic (semaglutide) has had its label expanded by the US Food and Drug Administration (FDA).
The agency approved the Danish drugmaker’s supplemental New Drug Application to market the therapy for the indication of reducing the risk of major adverse cardiovascular (CV) events including CV death, non-fatal heart attack, or non-fatal stroke in adults with type 2 diabetes and established CV 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