The global treatment market for Fabry disease will expand in value from $683 million in 2014 to approximately $1.25 billion by 2024, driven primarily by rising physician awareness of the condition and consequently higher diagnosis rates, a new study finds.
According to research and consulting firm GlobalData’s latest report, this value increase, which will occur across the seven major markets (7MM) of the USA, France, Germany, Italy, Spain, UK, and Japan, represents a moderate compound annual growth rate (CAGR) of 6.3%.
Valentina Gburcik, GlobalData’s director of cardiovascular and metabolic disorders, says that alongside increasing diagnosed cases, the market entry of the first pharmacological chaperone for the treatment of Fabry disease, namely Amicus Therapeutics’ (Nasdaq: FOLD) migalastat, will also boost growth.
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