French pharma major Sanofi (Euronext: SAN) and USA-based Regeneron Pharmaceuticals (Nasdaq: REGN) have announced that two Phase IIIb/IV trials of Praluent (alirocumab) successfully met their primary endpoints.
The companies are awaiting key data from the ODYSSEY OUTCOMES trial, which could establish whether they can outshine rival medication Repatha (evolocumab), which is being developed by Amgen (Nasdaq: AMGN), and has also had positive clinical results.
The firms are also locked in a lengthy patent dispute, which could result in Praluent being withdrawn from sale in the USA.
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