Japanese drugmaker Daiichi Sankyo (TYO: 4568) yesterday announced that the US Patent and Trademark Office (US PTO) rendered a Final Written Decision invalidating all claims of Seagen’s US patent 10,808,039 (the ’039 patent) that were challenged by Daiichi Sankyo in a post-grant review proceeding (PGR).
Seagen, which is ow a subsidiary of US pharma giant Pfizer (NYSE: PFE), argues that the linker and other ADC technology used in Daiichi’s HER2-directed antibody-drug conjugate (ADC) Enhertu (trastuzumab deruxtecan) are only "improvements" to technology licensed by the Japanese drugmaker, but which Seagen says it still owns.
“We are pleased that the US PTO invalidated all challenged claims of the ’039 patent,” said Naoto Tsukaguchi, corporate officer and general counsel, Daiichi Sankyo.
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