US firm Acucela and Japan's Otsuka Pharmaceutical have entered into a definitive agreement to co-develop rebamipide ophthalmic suspension, the latter's proprietary compound for the treatment of dry eye which is currently in Phase III clinical development in the USA.
Under the accord, the parties will collaborate in the clinical development efforts for rebamipide in the USA, with Acucela spearheading the regulatory strategy to gain approval for the product in America. On the grant of this, the parties may negotiate the terms under which Acucela may co-promote the product.
Otsuka will make an undisclosed cash upfront payment to Acucela, as well as clinical development milestones and a royalty on sales of the product. Otsuka will be responsible for all clinical development and commercialization expenses.
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