US pharma giant Pfizer (NYSE: PFE) today announced further positive data for its recently acquired Adcetris (brentuximab vedotin).
A Phase III study of the antibody-drug conjugate Adcetris in combination with lenalidomide and rituximab for the treatment of patients with relapsed/refractory diffuse large B-cell lymphoma (DLBCL) showed a statistically-significant and clinically-meaningful improvement in overall survival (OS) compared to lenalidomide and rituximab plus placebo. Positive outcomes were also observed in key secondary endpoints, including progression free survival (PFS) and overall response rate (ORR).
Adcetris was developed by US biotech Seagen, and was one of the main attractions for Pfizer’s recent acquisition of the company, notching up sales of around $751 million in the last nine months of 2023 under Seagen’s stewardship. Also included in the buy was Padcev (enfortumab vedotin).
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