In an announcement that has been widely anticipated, Maryland, USA-based biotechnology firm GenVec presented encouraging clinical and preclinical malaria vaccine data at the Keystone Symposium - Malaria: New Approaches to Understanding Host-Parasite Interactions taking place this week in Copper Mountain, Colorado.
Data from the Phase I/IIa malaria trial using GenVec technology indicate malaria vaccines given to malaria-naive adults were found to be safe and well-tolerated with minimal local or systemic reactions and no serious vaccine-related adverse reactions. Sterile protection, a complete absence of parasites in the blood, was seen in four out of 15 volunteers that had been inoculated with the vaccine and subsequently challenged with the malaria parasite.
This clinical trial is being conducted under sponsorship from the US Army Medical Materiel Development Activity and with financial support from the US Agency for International Development, the Congressionally Directed Peer Review Medical Program and the Military Infectious Diseases Research 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 2024 | Headless Content Management with Blaze