US biopharma company Ardelyx (Nasdaq: ARDX) says it has entered into a termination agreement with Anglo-Swedish pharma major AstraZeneca (LSE: AZN), such that all the rights to Ardelyx' portfolio of NHE3 inhibitors, including its lead product candidate, tenapanor, are returned to Ardelyx.
The decision comes about a month after Ardelyx announced that tenapanor failed to meet the primary endpoint of a Phase IIa clinical trial in patients with Stage 3 chronic kidney disease with type 2 diabetes mellitus and albuminuria (The Pharma Letter May 6). Under the terms of the agreement, AstraZeneca was obliged to communicate to Ardelyx on or before June 29, whether it will continue the development of tenapanor.
Ardelyx will pay AstraZeneca $25 million under termination terms
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