By Barbara Obstoj-Cardwell. Editor
Notable news last week including the UK’s GSK on Monday announcing it is withdrawing the US marketing authorization for its multiple myeloma drug Blenrep. The same day, the US Food and Drug Administration (FDA) approved the first one-time hemophilia B treatment, Hemgenix, developed by Dutch firm uniQure and to be marketed in the USA by CSL Behring. Last Wednesday, US biotech Arvinas released data from a Phase III trial of its breast cancer candidate ARV-471. Also of note, BioMarin had some good news, when it revealed that the FDA had done a U-turn on its review of hemophilia A candidate Roctavian, saying it would not after all hold an advisory committee evaluation of the product.
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