Sanofi (Euronext: SAN) has presented positive data from the Phase III ATLAS-PPX study of its once-monthly hemophilia therapy fitusiran.
People in the trial had severe hemophilia A or B and had previously been treated with prior factor or bypassing agent prophylaxis.
The results, presented in a late-breaking session at the annual meeting of the International Society on Thrombosis and Haemostasis (ISTH), show the trial met its primary endpoint, significantly reducing bleeding episodes.
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