US biotech Moderna (Nasdaq: MRNA) has reported encouraging early-stage results from a trial of its experimental vaccine for avian influenza, just as a significant federal funding agreement was unexpectedly withdrawn.
The investigational shot, known as mRNA-1018, is being developed as a countermeasure against H5 avian flu viruses. In a Phase I/II trial involving around 300 healthy adults, the vaccine prompted a strong immune response. According to Moderna, nearly all participants had protective levels of antibodies following the two-dose regimen, with a substantial rise in antibody titers from baseline. Reported side effects were generally mild or moderate.
Moderna chief executive Stéphane Bancel said the data “underscore the critical role mRNA technology has played as a countermeasure to emerging health threats.” He acknowledged that the loss of government backing introduces uncertainty but said the company would consider other options to continue the program.
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