Copenhagen, Denmark-based drugmaker H Lundbeck says that new data further demonstrate the effectiveness of its drug Ebixa (memantine) in the treatment of moderate-to-severe Alzheimer's disease.
In the meta-analysis of 1,826 subjects from six international Phase III placebo-controlled six-month studies, patients with moderate to severe AD showed statistically-significant benefit in favour of Ebixa treatment over placebo for key AD domains including function, cognition and global performance.
The firm noted that its N-methyl-D-aspartate receptor antagonist also significantly prevented clinical worsening of symptoms compared to placebo, which can be seen as a clinically-meaningful treatment goal.
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