Due to the US Food and Drug Administration's approval of the cosmetic filler Perlane (hyaluronic acid), Swedish biotechnology firm Q-Med has received $29.1 million from its local licensee Medicis. The payment is the last additional purchase sum from their 2006 agreement which has generated $160.0 million in total. Furthermore, Q-Med has exclusive manufacturing rights for the North American market for 10 years.
In connection with the payment, the previous provision of 34.5 Swedish kronor ($5.1 million) for R&D costs will be reversed. The first deliveries of Perlane will soon be made, according to Q-Med.
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