The marketing drive for Shire’s (LSE: SHP) Takhzyro (lanadelumab) has had a boost as the company seeks to convince payers that its hefty price tag is worth paying.
Takhzyro this year became the first monoclonal antibody of its kind to be approved to treat hereditary angioedema (HAE) in the USA and Canada, but it does face competition from CSL Behring’s Haegarda (C1 esterase inhibitor).
Both therapies were found to exceed commonly cited thresholds for cost-effectiveness by the Institute for Clinical and Economic Review (ICER), so the Ireland-headquartered company needs to convince physicians of the benefits of treatment with Takhzyro.
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