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

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A phase 2b randomized, controlled trial of the efficacy of the GMZ2 malaria vaccine in African children. / Sirima, Sodiomon B; Mordmüller, Benjamin; Milligan, Paul; Ngoa, Ulysse Ateba; Kironde, Fred; Atuguba, Frank; Tiono, Alfred B; Issifou, Saadou; Kaddumukasa, Mark; Bangre, Oscar; Flach, Clare; Christiansen, Michael; Bang, Peter; Chilengi, Roma; Jepsen, Søren; Kremsner, Peter G; Theisen, Michael.

In: Vaccine, Vol. 34, No. 38, 08.2016, p. 4536-4542.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Sirima, SB, Mordmüller, B, Milligan, P, Ngoa, UA, Kironde, F, Atuguba, F, Tiono, AB, Issifou, S, Kaddumukasa, M, Bangre, O, Flach, C, Christiansen, M, Bang, P, Chilengi, R, Jepsen, S, Kremsner, PG & Theisen, M 2016, 'A phase 2b randomized, controlled trial of the efficacy of the GMZ2 malaria vaccine in African children', Vaccine, vol. 34, no. 38, pp. 4536-4542. https://doi.org/10.1016/j.vaccine.2016.07.041

APA

Sirima, S. B., Mordmüller, B., Milligan, P., Ngoa, U. A., Kironde, F., Atuguba, F., Tiono, A. B., Issifou, S., Kaddumukasa, M., Bangre, O., Flach, C., Christiansen, M., Bang, P., Chilengi, R., Jepsen, S., Kremsner, P. G., & Theisen, M. (2016). A phase 2b randomized, controlled trial of the efficacy of the GMZ2 malaria vaccine in African children. Vaccine, 34(38), 4536-4542. https://doi.org/10.1016/j.vaccine.2016.07.041

Vancouver

Sirima SB, Mordmüller B, Milligan P, Ngoa UA, Kironde F, Atuguba F et al. A phase 2b randomized, controlled trial of the efficacy of the GMZ2 malaria vaccine in African children. Vaccine. 2016 Aug;34(38):4536-4542. https://doi.org/10.1016/j.vaccine.2016.07.041

Author

Sirima, Sodiomon B ; Mordmüller, Benjamin ; Milligan, Paul ; Ngoa, Ulysse Ateba ; Kironde, Fred ; Atuguba, Frank ; Tiono, Alfred B ; Issifou, Saadou ; Kaddumukasa, Mark ; Bangre, Oscar ; Flach, Clare ; Christiansen, Michael ; Bang, Peter ; Chilengi, Roma ; Jepsen, Søren ; Kremsner, Peter G ; Theisen, Michael. / A phase 2b randomized, controlled trial of the efficacy of the GMZ2 malaria vaccine in African children. In: Vaccine. 2016 ; Vol. 34, No. 38. pp. 4536-4542.

Bibtex

@article{1585affe2bd14560ae22a5c96648a991,
title = "A phase 2b randomized, controlled trial of the efficacy of the GMZ2 malaria vaccine in African children",
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 12-60months old were randomized to receive three injections of either 100μg 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/μL.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.",
author = "Sirima, {Sodiomon B} and Benjamin Mordm{\"u}ller and Paul Milligan and Ngoa, {Ulysse Ateba} and Fred Kironde and Frank Atuguba and Tiono, {Alfred B} and Saadou Issifou and Mark Kaddumukasa and Oscar Bangre and Clare Flach and Michael Christiansen and Peter Bang and Roma Chilengi and S{\o}ren Jepsen and Kremsner, {Peter G} and Michael Theisen",
note = "Copyright {\textcopyright} 2016 Elsevier Ltd. All rights reserved.",
year = "2016",
month = aug,
doi = "10.1016/j.vaccine.2016.07.041",
language = "English",
volume = "34",
pages = "4536--4542",
journal = "Vaccine",
issn = "0264-410X",
publisher = "Elsevier",
number = "38",

}

RIS

TY - JOUR

T1 - A phase 2b randomized, controlled trial of the efficacy of the GMZ2 malaria vaccine in African children

AU - Sirima, Sodiomon B

AU - Mordmüller, Benjamin

AU - Milligan, Paul

AU - Ngoa, Ulysse Ateba

AU - Kironde, Fred

AU - Atuguba, Frank

AU - Tiono, Alfred B

AU - Issifou, Saadou

AU - Kaddumukasa, Mark

AU - Bangre, Oscar

AU - Flach, Clare

AU - Christiansen, Michael

AU - Bang, Peter

AU - Chilengi, Roma

AU - Jepsen, Søren

AU - Kremsner, Peter G

AU - Theisen, Michael

N1 - Copyright © 2016 Elsevier Ltd. All rights reserved.

PY - 2016/8

Y1 - 2016/8

N2 - 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 12-60months old were randomized to receive three injections of either 100μg 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/μL.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.

AB - 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 12-60months old were randomized to receive three injections of either 100μg 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/μL.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.

U2 - 10.1016/j.vaccine.2016.07.041

DO - 10.1016/j.vaccine.2016.07.041

M3 - Journal article

C2 - 27477844

VL - 34

SP - 4536

EP - 4542

JO - Vaccine

JF - Vaccine

SN - 0264-410X

IS - 38

ER -

ID: 165010179