TY - JOUR
T1 - Extended follow-up of children in a phase2b trial of the GMZ2 malaria vaccine
AU - Dassah, Sylvester
AU - Adu, Bright
AU - Sirima, Sodiomon B.
AU - Mordmüller, Benjamin
AU - Ngoa, Ulysse Ateba
AU - Atuguba, Frank
AU - Arthur, Fareed K.N.
AU - Mensah, Benedicta A.
AU - Kaddumukasa, Mark
AU - Bang, Peter
AU - Kremsner, Peter G.
AU - Mategula, Donnie
AU - Flach, Clare
AU - Milligan, Paul
AU - Theisen, Michael
N1 - Publisher Copyright:
© 2021 The Authors
PY - 2021/7/13
Y1 - 2021/7/13
N2 - Background: The GMZ2/alum candidate malaria vaccine had an efficacy of 14% (95% confidence interval [CI]: 3.6%, 23%) against clinical malaria over 6 months of follow-up in a phase2b multicentre trial in children 1–5 years of age. Here we report the extended follow up of safety and efficacy over 2 years. Methods: A total of 1849 (GMZ2 = 926, rabies = 923) children aged 12–60 months were randomized to receive intramuscularly, either 3 doses of 100 μg GMZ2/alum or 3 doses of rabies vaccine as control 28 days apart. The children were followed-up for 24 months for clinical malaria episodes and adverse events. The primary endpoint was documented fever with parasitaemia of at least 5000/μL. Results: There were 2,062 malaria episodes in the GMZ2/alum group and 2,115 in the rabies vaccine group in the intention-to-treat analysis, vaccine efficacy (VE) of 6.5% (95%: CI −1.6%, 14.0%). In children aged 1–2 years at enrolment, VE was 3.6% (95 %CI: −9.1%, 14.8%) in the first year and −4.1% (95 %CI: −18.7%, 87%) in the second year. In children aged 3–5 years at enrolment VE was 19.9% (95 %CI: 7.7%, 30.4%) in the first year and 6.3% (95 %CI: −10.2%, 20.3%) in the second year (interaction by year, P = 0.025, and by age group, P = 0.085). A total of 187 (GMZ2 = 91, rabies = 96) serious adverse events were recorded in 167 individuals over the entire period of the study. There were no GMZ2 vaccine related serious adverse events. Conclusions: GMZ2/alum was well tolerated. Follow-up over 2 years confirmed a low level of vaccine efficacy with slightly higher efficacy in older children, which suggests GMZ2 may act in concert with naturally acquired immunity.
AB - Background: The GMZ2/alum candidate malaria vaccine had an efficacy of 14% (95% confidence interval [CI]: 3.6%, 23%) against clinical malaria over 6 months of follow-up in a phase2b multicentre trial in children 1–5 years of age. Here we report the extended follow up of safety and efficacy over 2 years. Methods: A total of 1849 (GMZ2 = 926, rabies = 923) children aged 12–60 months were randomized to receive intramuscularly, either 3 doses of 100 μg GMZ2/alum or 3 doses of rabies vaccine as control 28 days apart. The children were followed-up for 24 months for clinical malaria episodes and adverse events. The primary endpoint was documented fever with parasitaemia of at least 5000/μL. Results: There were 2,062 malaria episodes in the GMZ2/alum group and 2,115 in the rabies vaccine group in the intention-to-treat analysis, vaccine efficacy (VE) of 6.5% (95%: CI −1.6%, 14.0%). In children aged 1–2 years at enrolment, VE was 3.6% (95 %CI: −9.1%, 14.8%) in the first year and −4.1% (95 %CI: −18.7%, 87%) in the second year. In children aged 3–5 years at enrolment VE was 19.9% (95 %CI: 7.7%, 30.4%) in the first year and 6.3% (95 %CI: −10.2%, 20.3%) in the second year (interaction by year, P = 0.025, and by age group, P = 0.085). A total of 187 (GMZ2 = 91, rabies = 96) serious adverse events were recorded in 167 individuals over the entire period of the study. There were no GMZ2 vaccine related serious adverse events. Conclusions: GMZ2/alum was well tolerated. Follow-up over 2 years confirmed a low level of vaccine efficacy with slightly higher efficacy in older children, which suggests GMZ2 may act in concert with naturally acquired immunity.
KW - Africa
KW - Children
KW - Efficacy
KW - GMZ2
KW - Malaria
KW - Plasmodium falciparum
KW - Vaccine
UR - http://www.scopus.com/inward/record.url?scp=85108514063&partnerID=8YFLogxK
U2 - 10.1016/j.vaccine.2021.06.024
DO - 10.1016/j.vaccine.2021.06.024
M3 - Article
C2 - 34175127
AN - SCOPUS:85108514063
SN - 0264-410X
VL - 39
SP - 4314
EP - 4319
JO - Vaccine
JF - Vaccine
IS - 31
ER -