US drugmaker AbbVie (NYSE: ABBV) presented data at the American Society of Hematology’s annual meeting, demonstrating the efficacy of its investigational compound venetoclax in acute myelogenous leukemia.
The venetoclax group in the Phase II study showed an overall response rate of 15.5%, with one patient achieving a complete response (also called complete remission), and four achieving complete response with incomplete blood count recovery.
Gary Gordon, vice president, oncology clinical development at AbbVie, said: “This is the first time we have reported results from the venetoclax Phase II clinical trial in AML. We believe venetoclax’s potential in this indication warrants further investigation. The results from this study and AbbVie’s other abstracts presented during ASH represent the continued progress of our strong blood cancer development program and demonstrate our commitment to discovering innovative treatment options.”
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