<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ali AM</submitter><funding>NIAID NIH HHS</funding><funding>Bill and Melinda Gates Foundation</funding><pagination>e02193-17</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6153844</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>62(10)</volume><pubmed_abstract>Amodiaquine plus artesunate is the recommended antimalarial treatment in many countries where malaria is endemic. However, pediatric doses are largely based on a linear extrapolation from adult doses. We pooled data from previously published studies on the pharmacokinetics of amodiaquine, to optimize the dose across all age groups. Adults and children with uncomplicated malaria received daily weight-based doses of amodiaquine or artesunate-amodiaquine over 3 days. Plasma concentration-time profiles for both the parent drug and the metabolite were characterized using nonlinear mixed-effects modeling. Amodiaquine pharmacokinetics were adequately described by a two-compartment disposition model, with first-order elimination leading to the formation of desethylamodiaquine, which was best descr</pubmed_abstract><journal>Antimicrobial agents and chemotherapy</journal><pubmed_title>Population Pharmacokinetics of the Antimalarial Amodiaquine: a Pooled Analysis To Optimize Dosing.</pubmed_title><pmcid>PMC6153844</pmcid><funding_grant_id>OPP1099191</funding_grant_id><funding_grant_id>R01 AI117001</funding_grant_id><pubmed_authors>Carn G</pubmed_authors><pubmed_authors>Adjei GO</pubmed_authors><pubmed_authors>Smith TA</pubmed_authors><pubmed_authors>Ali AM</pubmed_authors><pubmed_authors>Goka BQ</pubmed_authors><pubmed_authors>Taylor W</pubmed_authors><pubmed_authors>Jones JJ</pubmed_authors><pubmed_authors>Alegre SS</pubmed_authors><pubmed_authors>Ouedraogo EB</pubmed_authors><pubmed_authors>WWARN Amodiaquine PK Study Group</pubmed_authors><pubmed_authors>Lwango R</pubmed_authors><pubmed_authors>Chotsiri P</pubmed_authors><pubmed_authors>Bruneel A</pubmed_authors><pubmed_authors>Aubouy A</pubmed_authors><pubmed_authors>Ouedraogo A</pubmed_authors><pubmed_authors>Ogutu B</pubmed_authors><pubmed_authors>Morgan CC</pubmed_authors><pubmed_authors>Denti P</pubmed_authors><pubmed_authors>Pinoges L</pubmed_authors><pubmed_authors>Gansane A</pubmed_authors><pubmed_authors>Obonyo C</pubmed_authors><pubmed_authors>Baudin E</pubmed_authors><pubmed_authors>Houze P</pubmed_authors><pubmed_authors>Penny MA</pubmed_authors><pubmed_authors>Faucher JF</pubmed_authors><pubmed_authors>Benakis A</pubmed_authors><pubmed_authors>Cammas M</pubmed_authors><pubmed_authors>Rodrigues OP</pubmed_authors><pubmed_authors>Sirima SB</pubmed_authors><pubmed_authors>Phyo AP</pubmed_authors><pubmed_authors>Jullien V</pubmed_authors><pubmed_authors>Alifrangis M</pubmed_authors><pubmed_authors>German P</pubmed_authors><pubmed_authors>Bertaux L</pubmed_authors><pubmed_authors>Kristensen K</pubmed_authors><pubmed_authors>Amedome H</pubmed_authors><pubmed_authors>Nosten F</pubmed_authors><pubmed_authors>Clark TD</pubmed_authors><pubmed_authors>Mwesigwa J</pubmed_authors><pubmed_authors>Branger M</pubmed_authors><pubmed_authors>Drysdale T</pubmed_authors><pubmed_authors>Schramm B</pubmed_authors><pubmed_authors>Dorsey G</pubmed_authors><pubmed_authors>Kiechel JR</pubmed_authors><pubmed_authors>Aweeka F</pubmed_authors><pubmed_authors>Hoegberg LCG</pubmed_authors><pubmed_authors>Sundaygar T</pubmed_authors><pubmed_authors>Sinou V</pubmed_authors><pubmed_authors>Day NPJ</pubmed_authors><pubmed_authors>McGready R</pubmed_authors><pubmed_authors>Parikh S</pubmed_authors><pubmed_authors>Guerin PJ</pubmed_authors><pubmed_authors>Mazinda CS</pubmed_authors><pubmed_authors>Juma E</pubmed_authors><pubmed_authors>Taudon N</pubmed_authors><pubmed_authors>Ashley EA</pubmed_authors><pubmed_authors>McGee B</pubmed_authors><pubmed_authors>Deloron P</pubmed_authors><pubmed_authors>Massougbodji A</pubmed_authors><pubmed_authors>Comte E</pubmed_authors><pubmed_authors>Doritchamou J</pubmed_authors><pubmed_authors>Simpson JA</pubmed_authors><pubmed_authors>Sasi P</pubmed_authors><pubmed_authors>Bergstrand M</pubmed_authors><pubmed_authors>Workman L</pubmed_authors><pubmed_authors>Parzy D</pubmed_authors><pubmed_authors>Tarning J</pubmed_authors><pubmed_authors>Sugnaux F</pubmed_authors><pubmed_authors>Win AK</pubmed_authors><pubmed_authors>Malaika LTM</pubmed_authors><pubmed_authors>Hsi P</pubmed_authors><pubmed_authors>Barnes KI</pubmed_authors><pubmed_authors>Annerberg A</pubmed_authors><pubmed_authors>Kossou H</pubmed_authors><pubmed_authors>Singhasivanon P</pubmed_authors><pubmed_authors>Valeh P</pubmed_authors><pubmed_authors>Cottrell G</pubmed_authors><pubmed_authors>Kamya MR</pubmed_authors><pubmed_authors>Rijken MJ</pubmed_authors><pubmed_authors>Adeothy A</pubmed_authors><pubmed_authors>Cot M</pubmed_authors><pubmed_authors>Kurtzhals JAL</pubmed_authors><pubmed_authors>Smith R</pubmed_authors><pubmed_authors>Zolia YM</pubmed_authors><pubmed_authors>Kalyango JN</pubmed_authors><pubmed_authors>Stepniewska K</pubmed_authors><pubmed_authors>Rosenthal PJ</pubmed_authors><pubmed_authors>Gourmel B</pubmed_authors><pubmed_authors>White NJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Population Pharmacokinetics of the Antimalarial Amodiaquine: a Pooled Analysis To Optimize Dosing.</name><description>Amodiaquine plus artesunate is the recommended antimalarial treatment in many countries where malaria is endemic. However, pediatric doses are largely based on a linear extrapolation from adult doses. We pooled data from previously published studies on the pharmacokinetics of amodiaquine, to optimize the dose across all age groups. Adults and children with uncomplicated malaria received daily weight-based doses of amodiaquine or artesunate-amodiaquine over 3 days. Plasma concentration-time profiles for both the parent drug and the metabolite were characterized using nonlinear mixed-effects modeling. Amodiaquine pharmacokinetics were adequately described by a two-compartment disposition model, with first-order elimination leading to the formation of desethylamodiaquine, which was best descr</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Oct</publication><modification>2026-06-14T04:20:38.649Z</modification><creation>2026-06-14T03:09:12.641Z</creation></dates><accession>S-EPMC6153844</accession><cross_references><pubmed>30038039</pubmed><doi>10.1128/AAC.02193-17</doi></cross_references></HashMap>