Finland-based Biotie Therapies (Nasdaq-OMX: BTH1V) says that, as it had already expected following disappointing clinical trial results, Belgian drugmaker UCB (Euronext Brussels: UCB) has confirmed that it does not intend to exercise its option to license its hydroxyphenylpyruvate dioxygenase (HPPD) inhibitor SYN118, under development for the treatment of Parkinson’s disease.
Results presented earlier this year from an exploratory Phase IIa study of SYN118 did not show a significant improvement in measures of PD motor function when compared to placebo.
SYN118 has been subject to an option agreement with UCB as part of a broader partnership for the development of new treatments for neurological disorders. At the time of the original data announcement, Biotie indicated that it did not expect UCB to exercise its option to license the compound based on the results generated in the Phase IIa study, a decision confirmed this week. Biotie has already fully impaired the carrying value of this asset due to the unlikelihood of UCB exercising their option.
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