The recent European Medicine Agency advisory committee, CHMP, positive opinion for French drug major Sanofi’s diabetes drug candidate Lyxumia (lixisenatide; The Pharma Letter November 19), its expected US New Drug Application filing next month and the potential European Union approval in first-quarter 2013, create a likely hat trick of positive catalysts for Denmark’s Zealand Pharma (Nasdaq OMX: ZEAL), which discover the GLP-1 receptor agonist, say analysts at Edison Equity Research.
However, a focus on monotherapy overlooks the fact that Zealand’s prospects rely more heavily on the “Fixflex” Lyxumia/Lantus combination. This is falling behind Novo Nordisk’s competing pairing of Tresiba (insulin degludec) – itself newly launched as monontherapy – with Victoza (liraglutide). This, combined with the relative advantages of Tresiba over Lantus, may constrain its commercial potential, the analysts note.
GetGoal data now in the net…
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