Since taking over as chief executive in July 2016, David Meek has overseen a period of near-seamless growth at French drugmaker Ipsen (Euronext: IPN), but he was hit by his first major setback on Friday.
The US Food and Drug Administration (FDA) has placed a partial clinical hold on studies of palovarotene for the chronic treatment of fibrodysplasia ossificans progressiva (FOP) and multiple osteochondromas (MO) in pediatric patients, news that led Ipsen to lose $2 billion in market capitalization in Friday’s trading.
On Friday, shares in Ipsen looked set to close more than 18% down on Thursday’s close, as markets digested the announcement. The hold applies to patients under the age of 14 years who are currently participating in the Phase II and III trials. The FDA is allowing the studies to continue to treat older patients.
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