California, USA-based Valentis suffered a serious setback on July 11, when the company revealed that there were no statistically-significant differences between the primary or secondary endpoints in a Phase IIb clinical trial of its peripheral arterial disease drug candidate VLTS 934. The news sent the firm's share price tumbling nearly 80% to $0.70. Commenting on the situation, chief executive Benjamin McGraw said: "the company has no plans for further development of the product and is assessing strategic opportunities, which include the sale or merger of the business, the sale of certain assets or other actions."
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