US drug developer Akebia Therapeutics (Nasdaq: AKBA) has entered into an exclusive agreement with Janssen Pharmaceutica, a subsidiary of Johnson & Johnson (NYSE: LNL), to license hypoxia inducible factor (HIF)-targeting product candidates.
The portfolio includes AKB-5169 (formerly JNJ5169), a differentiated preclinical compound in development as an oral treatment for inflammatory bowel disease (IBD). The agreement, facilitated by Johnson & Johnson Innovation, also provides Akebia with access to an extensive proprietary library of well-characterized HIF pathway compounds with potential applications across multiple therapeutic areas.
Under the terms of the multi-year research agreement, Akebia will pay Janssen $1.0 million in cash to access their collection of hundreds of HIF-targeted compounds and associated intellectual property. Importantly, Akebia obtains worldwide rights to AKB-5169, a non-absorbed oral HIF stabilizer in preclinical development for the treatment of IBD. Preclinical data have shown that AKB-5169 may be highly differentiated from standard of care systemic therapies in its potential to reduce inflammation and promote mucosal healing at the site of disease.
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