Anglo-Swedish drug major AstraZeneca (LSE: AZN) has entered into a settlement agreement in its US patent infringement litigation against USA-based Watson Laboratories, Actavis (NYSE: ACT; formerly known as Watson Pharmaceuticals but changed its trading name after acquiring Actavis), and Hungarian drugmaker EGIS Pharmaceuticals regarding Watson’s proposed rosuvastatin zinc product.
Watson, a successor of Cobalt, also agreed not to further appeal a decision by the US Court of Appeals for the Federal Circuit that upheld the validity and enforceability of the AstraZeneca’s blockbuster cholesterol lowerer Crestor (rosuvastatin calcium) substance patent. Japan’s Shionogi, AstraZeneca’s partner, is also a party to the settlement agreement.
Under the accord, Watson and EGIS concede that the Crestor substance patent is valid, enforceable and would be infringed by Watson’s rosuvastatin zinc product and its rosuvastatin calcium product. Crestor, for which patents were recently invalidated in Australia (The Pharma Letter March 5), is expected to generate global revenues of some $6 billion this year, having hit $6.25 billion in 2012, around half of which comes from the USA.
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