Study design

BA Bayode R. Adegbite
JE Jean R. Edoa
YH Yabo J. Honkpehedji
FZ Frejus J. Zinsou
JD Jean C. Dejon-Agobe
MM Mirabeau Mbong-Ngwese
FL Fabrice Lotola-Mougueni
EK Erik Koehne
AL Albert Lalremruata
AK Andrea Kreidenweiss
TN The T. Nguyen
JK Jutta Kun
SA Selidji T. Agnandji
BL Bertrand Lell
AS Abdou R. Safiou
FA Fridia A. Obone Atome
GM Ghyslain Mombo-Ngoma
MR Michael Ramharter
TV Thirumalaisamy P. Velavan
BM Benjamin Mordmüller
PK Peter G. Kremsner
AA Ayola A. Adegnika
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The study was an open-label clinical trial with a sequential enrolment of patients treated with AL or AS–AQ. After 50 children were treated with AL, another 50 children received AS–AQ. The primary objective was to assess the PCR corrected cure rates at day 28; the secondary objectives were to assess patterns of fever and parasite clearance; changes in haemoglobin levels after treatment by AL or AS–AQ as well as their safety and tolerability; and investigate the presence of artemisinin resistance molecular markers.

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