The US Food and Drug Administration has approved Jemperli (dostarlimab-gxly), a checkpoint blocker developed by UK drugmaker GlaxoSmithKline (LSE: GSK).
The therapy has been approved for the treatment of certain adults with recurrent or advanced endometrial cancer, as a second-line option after chemotherapy.
Chief scientific officer Hal Barron said the decision “has the potential to transform the treatment landscape for these women and demonstrates our continued commitment to helping patients with gynecologic cancers.”
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