Viventia Biotech, a privately-held Canadian biopharmaceutical company focused on cancer, says that in vitro cytotoxicity and in vivo pharmacokinetic studies conducted to evaluate the potential for combining its lead anticancer drug, Proxinium (VB4-845), with first-line standard-of-care therapy for squamous cell carcinoma of the head and neck, were positive.
The data, which were presented at the annual meeting of the American Association for Cancer Research, held in Los Angeles, California, found that the combination of Proxinium with cisplatin, carboplatin, paclitaxel, 5-fluorouracil, and docetaxel resulted in a significant additive cytotoxic effect (p<0.05) as compared to the chemotherapeutic agents administered alone.
Proxinium is being developed to treat late-stage, locally-advanced head and neck cancer and is currently enrolling patients in the TARGET trial, a pivotal Phase III global evaluation that is expected to complete patient recreuitment by the end of the year.
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