A monoclonal antibody therapeutic drug, a novel approach to treating patients with influenza, will advance in development with funding from the US Department of Health and Human Services’ Office of the Assistant Secretary for Preparedness and Response (ASPR).
No monoclonal antibody antiviral drugs to treat patients with influenza have been approved by the US Food and Drug Administration. Monoclonal antibodies bind to specific parts of the virus, neutralizing the virus and decreasing the amount of virus in the body.
VIS410 being developed by Visterra
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 2025 | Headless Content Management with Blaze