The USA’s MEI Pharma (Nasdaq: MEIP) has announced the execution of a license agreement granting Japan’s Kyowa Hakko Kirin (TYO: 4151) exclusive rights to develop and commercialize ME-401 in Japan.
ME-401 is MEI's phosphatidylinositol 3-kinase (PI3K) delta inhibitor being developed by MEI for the treatment of patients with B-cell malignancies. MEI is planning to initiate a Phase II study to evaluate patients with follicular lymphoma that is intended to support an accelerated approval marketing application with the US Food and Drug Administration.
Financial terms of the collaboration
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