The German Institute for Quality and Efficiency in Health Care (IQWiG) has assessed Vyndaqel (tafamidis), a treatment for a rate neurological disorder the pharma behemoth Pfizer (NYSE: PFE), at the request of the Federal Joint Committee (G-BA), saying that it has found “a hint of a positive effect” of tafamidis on neurological degeneration.
Vyndaqel was approved by the European Commission last year for the treatment of transthyretin amyloidosis in adults (The Pharma Letter November 18, 2011). This rare disorder (orphan disease) is caused by a defective gene and is associated with progressive nerve damage (neurological degeneration) that tafamidis is supposed to delay, the IQWiG noted.
Tafamidis compared with "best supportive care"
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