Belgian cell therapy company TiGenix (Euronext Brussels: EBR) has appointed Marie Paule Richard as chief medical officer, and Mary Carmen Diez as its vice president of medical affairs and new product commercialization.
Dr Richard has previously held the same position at Aicuris in Germany, as well as high-level medical officer positions at Crucell in Switzerland and France’s Sanofi Pasteur, leading development and regulatory approval of several products in Europe and the USA. At TiGenix, she will head the development of Cx611 in early rheumatoid arthritis and severe sepsis, as well as completing ongoing European Phase III studies for Cx601 in Crohn’s disease, and its preparation of an American developmental plan for the drug.
Dr Diez has more than 20 years’ experience in the biopharma industry, and joins TiGenix from Meda Pharma, where she was an international medical marketing director for nine years, during which time she launched several products in Europe. She has also worked at Asta Medica, Pfizer and Dupont. She will now be responsible for preparing the launch of Cx601 in Europe.
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