Vertex Pharmaceuticals (Nasdaq: VRTX) is another step closer to realizing its ambitious goal of treating every person with cystic fibrosis (CF) and to ensuring healthy revenue figures for the year ahead.
The Boston-based biotech has received approval from the US Food and Drug Administration (FDA) for another of its CF drugs, the third that it can sell in the USA. Vertex already has approval for Kalydeco (ivacaftor) and Orkambi (lumacaftor/ivacaftor), and its newly-approved treatment, called Symdeko, is a combination of Kalydeco and a new medicine called tezacaftor.
Symdeko, which has been approved for treating the underlying cause of CF in people ages 12 and older who have two copies of the F508del mutation in the cystic fibrosis transmembrane conductance regulator gene or who have at least one mutation that is responsive to tezacaftor/ivacaftor, will have a list price of $292,000 per year, a level between Kalydeco and Orkambi.
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