The US regulator has agreed to review a filing for the investigational medicine tucatinib, in combination with trastuzumab and chemotherapy, under Priority Review.
The submission, from Seattle Genetics (Nasdaq:SGEN), is for the treatment of people with locally advanced unresectable or metastatic HER2-positive breast cancer, in a later-line setting.
Tucatinib, a tyrosine kinase inhibitor (TKI) that is highly selective for HER2, was brought on board through the firm’s $614 million acquisition of Cascadian Therapeutics in 2018, a deal which now looks to have been worth every penny.
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