Boehringer Ingelheim today announced that it has decided to discontinue treatment in the Phase II trial of a novel, first-in-class compound for reducing the risk or severity of acute respiratory distress syndrome (ARDS) in patients hospitalized for COVID-19 and requiring non-invasive oxygen support.
This decision by the German family-owned is based on the recommendation of the trial’s independent Data Monitoring Committee after an interim look at unblinded safety and efficacy data showing a clear lack of benefit for use of BI 764198 in patients hospitalized for COVID-19 and needing oxygen support.
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