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A phase 2b randomized, controlled trial of the efficacy of the GMZ2 malaria vaccine in African children

Journal Article
Published: March 10, 2025
Authors
Tiono AB
Sirima SB
GMZ2 Trial Study Grp
Mordmuller B
Milligan P
Ngoa UA
Kironde F
Atuguba F
Issifou S
Kaddumukasa M
Bangre O
Flach C
Christiansen M
Bang P
Chilengi R
Jepsen S
Kremsner PG
Theisen M
Abstract

Background: GMZ2 is a recombinant protein malaria vaccine, comprising two blood-stage antigens of Plasmodium falciparum, glutamate-rich protein and merozoite surface protein 3. We assessed efficacy of GMZ2 in children in Burkina Faso, Gabon, Ghana and Uganda.Methods: Children 12-60 months old were randomized to receive three injections of either 100 mu g GMZ2 adjuvanted with aluminum hydroxide or a control vaccine (rabies) four weeks apart and were followed up for six months to measure the incidence of malaria defined as fever or history of fever and a parasite density >= 5000/mu L.Results: A cohort of 1849 children were randomized, 1735 received three doses of vaccine (868 GMZ2, 867 control-vaccine). There were 641 malaria episodes in the GMZ2/Alum group and 720 in the control group. In the ATP analysis, vaccine efficacy (VE), adjusted for age and site was 14% (95% confidence interval [CI]: 3.6%, 23%, p-value = 0.009). In the ITT analysis, age-adjusted VE was 11.3% (95% CI 2.5%, 19%, p-value = 0.013). VE was higher in older children. In GMZ2-vaccinated children, the incidence of malaria decreased with increasing vaccine-induced anti-GMZ2 IgG concentration. There were 32 cases of severe malaria (18 in the rabies vaccine group and 14 in the GMZ2 group), VE 27% (95% CI -44%, 63%).Conclusions: GMZ2 is the first blood-stage malaria vaccine to be evaluated in a large multicenter trial. GMZ2 was well tolerated and immunogenic, and reduced the incidence of malaria, but efficacy would need to be substantially improved, using a more immunogenic formulation, for the vaccine to have a public health role. (C) 2016 Elsevier Ltd. All rights reserved.

Details
DOI
10.1016/j.vaccine.2016.07.041
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