US drugmaker MedImmune says that data from a pivotal Phase III study of its next-generation, investigational influenza vaccine, CAIV-T (cold adapted influenza vaccine, trivalent), showed it to be 55% more effective than the trivalent injectable inactivated influenza vaccine in reducing illness caused by any influenza strain in children six months to 59 months of age.
According to the San Francisco-headquartered company, the study also showed that CAIV-T provided statistically-significant improvements in reducing influenza illness caused by both matched and mismatched A strains as compared to the flu shot. MedImmune says it will submit the data to domestic regulators in June, seeking an expanded label for the product to include children aged from five years to as young as six months.
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