Population pharmacokinetics of artemether–lumefantrine plus amodiaquine in patients with uncomplicated Plasmodium falciparum malaria
6
Issued Date
2025-01-01
Resource Type
ISSN
03065251
eISSN
13652125
Scopus ID
2-s2.0-105018482339
Pubmed ID
41052792
Journal Title
British Journal of Clinical Pharmacology
Rights Holder(s)
SCOPUS
Bibliographic Citation
British Journal of Clinical Pharmacology (2025)
Suggested Citation
Ding J., Hoglund R.M., van der Pluijm R.W., Callery J.J., Peto T.J., Tripura R., Das S., Châu N.H., Promnarate C., Mukaka M., Dysoley L., Fanello C., Onyamboko M.A., Anvikar A.R., Mayxay M., Smithuis F., von Seidlein L., Dhorda M., Amaratunga C., Faiz M.A., Nghia H.D.T., White N.J., Day N.P.J., Dondorp A.M., Tarning J. Population pharmacokinetics of artemether–lumefantrine plus amodiaquine in patients with uncomplicated Plasmodium falciparum malaria. British Journal of Clinical Pharmacology (2025). doi:10.1002/bcp.70301 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/112674
Title
Population pharmacokinetics of artemether–lumefantrine plus amodiaquine in patients with uncomplicated Plasmodium falciparum malaria
Author(s)
Author's Affiliation
Nuffield Department of Medicine
Mahidol Oxford Tropical Medicine Research Unit
Université de Kinshasa
Oxford University Clinical Research Unit
National Institute of Malaria Research India
Ministry of Health Laos
National Center for Parasitology
Myanmar Oxford Clinical Research Unit
Pham Ngoc Thach University of Medicine
Dev Care Foundation
Mahidol Oxford Tropical Medicine Research Unit
Université de Kinshasa
Oxford University Clinical Research Unit
National Institute of Malaria Research India
Ministry of Health Laos
National Center for Parasitology
Myanmar Oxford Clinical Research Unit
Pham Ngoc Thach University of Medicine
Dev Care Foundation
Corresponding Author(s)
Other Contributor(s)
Abstract
Aims: Resistance to the artemisinins and the artemisinin-based combination therapy (ACT) partner drugs has developed in Southeast Asia, and artemisinin resistance has also emerged in eastern Africa. Triple ACTs (triple artemisinin-based combination therapies, TACT), consisting of two partner drugs with different mechanisms of action and similar pharmacokinetic profiles, combined with an artemisinin derivative can help to delay or prevent artemisinin resistance and prolong the useful lifetime of the partner drugs. This study aims to characterize the pharmacokinetic properties of a recommended TACT, artemether-lumefantrine plus amodiaquine, using data from two large clinical trials. Methods: We analysed data from two randomized, controlled intervention trials conducted between 2015 and 2020 in one African country and two Southeast Asian countries, in which artemether-lumefantrine was administered alone (n = 443) or together with amodiaquine (n = 442) to patients with uncomplicated P. falciparum malaria. Both studies included a sub-cohort with dense pharmacokinetic sampling, combined with sparse data in the other patients. Concentration–time data of artemether, dihydroartemisinin, lumefantrine, desbutyllumefantrine, amodiaquine and desethylamodiaquine were analysed using nonlinear mixed-effects modelling. Results: Pharmacokinetic models were developed for all drugs and demonstrated good predictive performance and goodness-of-fit diagnostics. Coadministered amodiaquine was not a significant covariate on pharmacokinetic properties of artemether-lumefantrine. Model-predicted C<inf>max</inf> and AUC (median [95% confidence interval, CI]) for artemether were 256 (159–407) ng/mL and 2850 (1820-4920) h·ng/mL for artemether-lumefantrine alone, and 230 (123–391) ng/mL and 2800 (1570-4570) h·ng/mL for artemether-lumefantrine-amodiaquine. For dihydroartemisinin, values were 135 (54.5–214) ng/mL and 1870 (813–3015) h·ng/mL for artemether-lumefantrine alone, and 116 (40.8–186) ng/mL and 1580 (547–2680) h·ng/mL for artemether-lumefantrine-amodiaquine. For lumefantrine, values were 15.2 (2.90–31.3) μg/mL and 600 (275–1230) h·μg/mL for artemether-lumefantrine alone, and 14.1 (2.72–31.4) μg/mL and 586 (269–1070) h·μg/mL for artemether-lumefantrine-amodiaquine. Day 7 concentrations of lumefantrine were 452 (215–1240) and 438 (204–1030) μg/mL for artemether-lumefantrine alone and artemether-lumefantrine-amodiaquine, respectively. All geometric mean ratios (GMRs) for the drug–drug interaction (DDI) effect on key pharmacokinetic parameters of artemether, dihydroartemisinin and lumefantrine fell within the 0.80–1.25 range, with the majority of the corresponding 90% CI also contained within this range. This indicates no clinically relevant DDIs between artemether-lumefantrine and amodiaquine. Conclusions: The DDI effect of amodiaquine on the pharmacokinetics of artemether-lumefantrine is expected to be minimal, the based on the current analysis. However, further large-scale clinical trials are needed to confirm this finding.