Corvas International has completed the planned enrollment of its PhaseIIa safety trial for the propriety injectable anticoagulant, recombinant Nematode Anticoagulant Protein c2, in patients undergoing elective percutaneous transluminal coronary angioplasty. Previous studies of the anticoagulant have shown it to be safe and effective in the prevention of deep vein thrombosis following unilateral knee replacement (Marketletter June 26, 2000). The data obtained from the current trial will be used in future studies to evaluate rNAPc2 in patients with acute coronary syndromes, such as unstable angina, and the company also intends to initiate two Phase III trials later this year which will compare rNAPc2 to low molecular weight heparin for the prevention of DVT in patients undergoing major orthopedic surgery.
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