The US subsidiary of Japanese drug major Astellas Pharma (TYO: 4503) and USA-based privately held firm Ambit Biosciences announced that they will end their collaboration for the joint development and commercialization of FMS-like tyrosine kinase-3 (FLT3) inhibitors, including quizartinib, effective September 3, 2013.
Astellas gained access to the program under a $390 million deal signed in 2009 (The Pharma Letter December 18, 2009). It has now exercised its right to terminate the worldwide license agreement, citing “strategic reasons,” and, over the months ahead, the companies will work together to transfer current development activities to Ambit. On the effective date of termination, Ambit will regain all rights granted to Astellas and continue with the quizartinib clinical trial program.
Michael Martino, president and chief executive of Ambit, said: “With the Phase II study results for quizartinib that were presented at the ASH Annual Meeting last year [TPL December 18, 2012], we and members of the medical community continue to be excited about quizartinib and its potential to meet a significant, unmet need in acute myeloid leukemia (AML) patients. We are fully committed to moving forward with the Phase III clinical trial plan and look forward to advancing this important drug candidate toward approval.”
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