A combination of Imbruvica (ibrutinib) and Rituxan/MabThera (Rituxan) has shown greater efficacy than the latter drug alone in patients with Waldenström’s macroglobulinemia (WM), a rare and incurable form of non-Hodgkin’s lymphoma (NHL).
The Phase III data featured as an oral presentation at the 2018 American Society of Clinical Oncology (ASCO) Annual Meeting, was selected for the Best of ASCO 2018 and simultaneously published in the New England Journal of Medicine.
Ibrutinib, a first-in-class Bruton's tyrosine kinase (BTK) inhibitor, is jointly developed and commercialized by Janssen Biotech, part of the Johnson & Johnson (NYSE: JNJ) group, and Pharmacyclics, an AbbVie (NYSE: ABBV) company. It is already approved as a monotherapy in WM.
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