Gilead Sciences (Nasdaq: GILD) has revealed promising five-year data from its Phase II ZUMA-5 trial of Yescarta (axicabtagene ciloleucel), at the American Society of Hematology meeting.
The study examines long-term survival in people with relapsed or refractory non-Hodgkin lymphomas. Data show an overall response rate of 90%, with 75% of patients achieving complete remission.
Lead investigator Sattva Neelapu said: “Relapsed or refractory non-Hodgkin lymphomas are generally considered incurable, with most patients ultimately relapsing,” adding: “These impressive results demonstrate the durable clinical benefit and manageable long-term safety profile of axi-cel and give us hope it may have a curative effect.”
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