The USA's Atrix Laboratories has reported that its licensee for Eligard (leuprolide acetate for injection), Sanofi-Synthelabo Canada, received notice of compliance from the Therapeutics Products Directorate of Health Canada, thereby permitting the product to be sold there. The notice refers to Eligard 30mg, a four-month sustained release treatment for prostate cancer. Sanofi is working to launch one-, three- and four-month products by May, notes the company. Eligard 7.5mg and 22.5mg one- and three-month prostate cancer products were approved in Canada last year (Marketletter November 17, 2003).
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