US biotech firm Dendreon (Nasdaq: DNDN) has released positive preliminary data from a long-term analysis of the Phase II STAND study with its prostate cancer drug Provenge (sipuleucel-T).
The study demonstrated that tumor-specific T-cell responses appear to be enhanced and sustained when Provenge is given after androgen deprivation therapy (ADT) in patients with biochemically-recurrent prostate cancer (BRPC) at high risk for metastases. These data will be presented at the 29th Annual European Association of Urology (EAU) Congress taking place from April 11-15, 2014 in Stockholm, Sweden.
“The presentation of these data at EAU highlights Dendreon’s commitment to expanding awareness and understanding of immunotherapy and Provenge in Europe as we prepare to make Provenge available to advanced prostate cancer patients beyond the United States.”
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