UCB of Belgium has been granted marketing approval across the EuropeanUnion for Xyzal/Xusal (levocetirizine), its new-generation non-sedating antihistamine product which was first registered in Germany earlier this year (Marketletter January 22). As in Germany, the drug has been approved in the EU for all three target indications, ie seasonal allergic rhinitis, perennial allergic rhinitis and chronic idiopathic urticaria.
Xyzal has already been launched in Germany and Switzerland, where reportedly strong initial sales helped UCB's antihistamine franchise, spearheaded by parent drug Zyrtec (cetirizine), rise 12% to 188 million euros ($171 million) in the first half of this year. Xyzal can be taken once-daily, as opposed to twice-daily dosing with Zyrtec, and boasts a "rapid onset of action, outstanding efficacy and an excellent safety profile," according to UCB.
Further EU launches in October
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 2025 | Headless Content Management with Blaze