While much hope was attached to the possible use of Gilead Sciences’ (Nasdaq: GILD) investigational antiviral remdesivir in the fight against the COVID-19 pandemic, last week early data from a study of the drug in China, published in error by the World Health Organization (WHO), seemed to kill off this idea, even though the company itself has yet to release results from its own research.
Responding to the situation, Gilead’s chief medical officer Dr Merdad Parsey noted that this information has since been removed, as the study investigators did not provide permission for the publication of the results.
Dr Parsey stated: “Furthermore, we believe the post included inappropriate characterizations of the study. The study was terminated early due to low enrollment and, as a result, it was underpowered to enable statistically-meaningful conclusions. As such, the study results are inconclusive, though trends in the data suggest a potential benefit for remdesivir, particularly among patients treated early in disease. We understand the available data have been submitted for peer-reviewed publication, which will provide more detailed information from this study in the near future.”
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