Rhone-Poulenc Rorer's taxoid compound Taxotere (docetaxel) has been approved in its first market, Mexico, for the treatment of untreated and previously-treated breast and non-small cell lung cancer. The company intends to launch the drug in Mexico by April, 1995. Taxotere is the second taxoid to reach the market after Bristol-Myers Squibb's Taxol (paclitaxel), which was first launched in the USA for ovarian cancer in 1993.
Taxotere is suitable for use on an outpatient basis, notes R-PR, with the recommended dose in the Mexican application being 100mg/m2 given intravenously for one hour every three weeks. Like Taxol, Taxotere requires a premedication regimen to reduce some of the side effects of the drug which are thought to arise from the medium in which it is suspended.
Applications for approval of Taxotere are pending with regulatory authorities around the world, notes R-PR, and the US Food and Drug Administration's Oncologic Drugs Advisory Committee will be reviewing the agent at its meeting tomorrow (December 13).
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