UK drug major GlaxoSmithKline says that the European Commission has granted Marketing Authorization for Hycamtin (topotecan powder for concentrate for solution for infusion) for the treatment of patients with relapsed small cell lung cancer for whom re-treatment with the first-line regimen is not considered appropriate.
Hycamtin is the first product to be approved in Europe that is specifically indicated for the treatment of relapsed SCLC. Data from its clinical evaluations demonstrated prolonged survival and quality of life compared to best supportive care in patients battling the disease.
The topoisomerase I inhibitor, which is already familiar to oncologists as a treatment for relapsed ovarian cancer, works by inducing DNA damage which results in the death of dividing cells.
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 2025 | Headless Content Management with Blaze