Canadian biopharmaceutical firm Bioniche Life Sciences has enrolled the first patient in a Phase III trial of its drug candidate Urocidin (mycobacterial cell wall-DNA complex) in refractory bladder cancer. The US Food and Drug Administration approved the company's refractory, open-label study in February of this year, and subsequently granted it Fast Track designation in April.
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