- A clinical trial with a polysaccharide conjugate vaccine for the prevention of group B streptococcus disease in newborns, young infants and adults, has demonstrated that the vaccine was well-tolerated with minimal reactogenicity and no serious side effects. Antibodies transported across the placenta may also be able to offer protection to premature babies. The technology has been licensed to North American Vaccine from Brigham and Women's Hospital and Harvard University in the USA.
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