UK specialist health care company BTG (LSE: BTG) and its partner, China-focused US specialty drugmaker SciClone Pharmaceuticals (Nasdaq: SCLN) have received approval for their DC Bead from the China Food and Drug Administration in the embolization of malignant hypervascularized tumors.
The two companies have an agreement whereby SciClone holds exclusive licensing and distribution rights for the therapy in China, which means SciClone will purchase product from BTG at a specified price for sale in the region.
Louise Makin, chief executive of BTG, said: “Approximately half of the world’s liver cancer patients are in China and there is a great interest among Chinese physicians to offer new, differentiated treatment options. Today’s news marks an important step toward bringing our first interventional oncology product, DC Bead, to the Chinese market where we can help address this need.”
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