The candidate vaccine called R21/Matrix-M showed up to 77 per cent efficacy in the year-long trial of 450 children
A potential new malaria vaccine has proved highly effective in a trial in babies in Africa, pointing to it one day possibly helping reduce the death toll from the mosquito-borne disease that kills up to half a million young children a year.
The candidate vaccine, developed by scientists at Britain’s University of Oxford and called R21/Matrix-M, showed up to 77 per cent efficacy in the year-long trial of 450 children in Burkina Faso, researchers leading the trial said in a statement.
The scientists, led by Adrian Hill, director of Oxford’s Jenner Institute and also one of the lead researchers behind the Oxford-AstraZeneca COVID-19 vaccine, said they now plan to conduct final stage trials in some 4,800 children aged between 5months and 3 years in four African Countries.
Hill said he had “high expectations for the potential of this vaccine” which he said would be the first against malaria to reach a World Health Organization (WHO) goal of a malaria shot with at least 75 per cent efficacy.
Scientists around the world have been working for decades to develop a vaccine to prevent malaria – a complex infection caused by a parasite carried in the saliva of mosquitoes.
Malaria infects millions of people every year and kills more than 400,000 – most of them babies and young children in the poorest parts of Africa.
The world’s first and only licensed malaria vaccine, Mosquirix, was developed by GlaxoSmithKline over many years of clinical trial across several African countries but is only partially effective at around 30%.
In the R21/Matrix-M trial in Burkina Faso, the 450 young children were divided into three groups. Two groups got three doses of the experimental vaccine along with either a low or a high dose of an adjuvant – an ingredient designed to super-charge the body’s response to a vaccine – while the third group was given a control vaccine.
Results, which researchers said would soon be published in The Lancet medical journal, showed the efficacy of 77 per cent in the high-dose adjuvant group and 74 per cent among those who got the vaccine with a low-dose of adjuvant.