USA-based Adventrx Pharmaceuticals, a specialist developer of anticancer and antiviral drugs, has announced positive efficacy and safety data from Phase II trials of its candidate compound CoFactor as a cancer treatment. The findings were presented at the 2006 Gastrointestinal Cancers Symposium in San Francisco, USA.
The results, which were confirmed by an independent radiology organization contracted by the firm to ensure objectivity, showed that the drug, in combination with 5-fluorouracil, yielded a clinical benefit of 85% in terms of objective response to treatment, defined as those patients having complete or partial tumor responses. The secondary study endpoint, time to tumor progression increased to 163 days. The drug was also well-tolerated with no grade three or four drug-related toxicity events recorded during the program.
Adventrx' executive vice president, Joan Robbins, said: "Cofactor plus 5-FU helped stabilize the overwhelming majority of these patients and did so with a minimum of serious hematological and gastrointestinal toxicity.
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