Novartis has backed out of its collaboration with CoCensys over thedevelopment of ACEA 1021, the latters' compound for the treatment of stroke and traumatic brain injury. CoCensys said that "the decision was influenced by preliminary results of a recently-completed Phase I safety trial."
ACEA 1021 is a glycine site antagonist, a class of compounds which rely for their activity on the fact that simultaneous binding of glycine and glutamate are required for NMDA channel activation. Several NMDA antagonists have been developed for the treatment of stroke, but most have not proceeded too far in development due to central nervous system side effects, such as hallucinations, delirium or agitation, or cardiovascular effects.
ACEA 1021 has already been studied in a series of Phase I clinical trials, and there has been no evidence of any dose-limiting CNS effects. However, the results of the most recent trial have indicated that in some patients crystals of ACEA 1021 have appeared in the urine, which is a potentially dose-limiting effect.
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