US drug major Eli Lilly has entered into a licensing and collaboration agreement with Transition Therapeutics granting the former exclusive worldwide rights to develop and commercialize its gastrin-based therapies, including the lead compound TT-223, which is currently in early Phase II testing. Gastrin based-therapies are an emerging class of potential disease-modifying agents for patients with diabetes, and have been shown to provide sustained improvement in glycemic control in preclinical models and early clinical studies.
Under the terms of the accord, Transition will get a $7.0 million upfront payment, and may also receive up to $130.0 million in potential development and sales milestones, as well as royalties on sales of gastrin-based therapies if any product is successfully commercialized. Transition and Lilly will both participate in the currently planned Phase II clinical trial with lead compound TT-223 in type 2 diabetes, after which Lilly will take responsibility. Other terms of the deal were not disclosed.
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 2025 | Headless Content Management with Blaze