Just days after agreeing acquisition terms with takeover suitor Sanofi-Aventis (Euronext: SAN; The Pharma Letter February 16), US biotech firm Genzyme (Nasdaq: GENZ) announced three-year follow-up data from patients enrolled in the Phase II clinical trial for its investigational oral therapy for Gaucher disease type 1, eliglustat tartrate, raising hope for a second treatment to add to its rare disease portfolio, which already includes Cerezyme (imiglucerase for injection) for Gaucher and Fabry disease agent Fabrazyme (agalsidase beta).
Sustained or further improvements were observed across all endpoints, including bone disease, at the three-year timepoint. The results were presented for the first time last week at the Lysosomal Disease Network WORLD Symposium in Las Vegas, Nevada, USA.
Could help restore lost sales
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