US-based Alza Corp and US Bioscience Inc have been granted marketing approval in the USA for expanded labelling for Ethyol (amifostine) to include use in patients with non-small cell lung cancer for the reduction of cumulative renal damage associated with repeated administration of cisplatin-based chemotherapy. Initial approval was given to US Bioscience in December 1995 to market Ethyol to reduce the cumulative kidney toxicity associated with cisplatin administration in patients with advanced ovarian cancer.
Ethyol will be marketed by Alza for an initial period of five years, during which time the US Bioscience sales force will co-promote the product. After this time, marketing rights on Ethyol will revert to US Bioscience. The product will be commercially available early this year.
According to the American Cancer Society, there will be an estimated 177,000 new cases of lung cancer in the USA this year. Non-small cell lung cancer accounts for approximately 75% of all lung cancers, and cisplatin is among the most frequently prescribed chemotherapeutic agents for this disease. Ethyol is given at the initiation of cisplatin-based therapy. By reducing kidney toxicity, Ethyol reduces the likelihood of delays or discontinuation of chemotherapy.
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 2025 | Headless Content Management with Blaze