In a second deal with the company, Ligand Pharmaceuticals (Nasdaq: LGND) has entered into a global licensing agreement with Chiva Pharmaceuticals, a US affiliate of Hong Kong-based Hainan Kaihua Pharmaceutical, for Fablyn (lasofoxifene), a selective estrogen receptor modulator (SERM) that was approved in the European Union in 2009 for the treatment of osteoporosis in post-menopausal women at increased risk of fracture.
In return, Ligand will receive $4 million in licensing payments over the next eight months and is also eligible to receive milestones and royalties on worldwide sales of Fablyn, the US firm noted.
Fablyn was discovered through a research collaboration between Ligand and Pfizer that began in 1991. The drug was fully developed by Pfizer through regulatory approval in the EU. After Pfizer acquired a similar SERM program, Conbriza (bazedoxifene), through its acquisition of Wyeth, Fablyn reverted to Ligand earlier this year.
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