<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>58(10)</volume><submitter>Manning J</submitter><pubmed_abstract>Dihydroartemisinin-piperaquine, the current first-line drug for uncomplicated malaria caused by Plasmodium falciparum and Plasmodium vivax in Cambodia, was previously shown to be of benefit as malaria chemoprophylaxis when administered as a monthly 3-day regimen. We sought to evaluate the protective efficacy of a compressed monthly 2-day treatment course in the Royal Cambodian Armed Forces. The safety and efficacy of a monthly 2-day dosing regimen of dihydroartemisinin-piperaquine were evaluated in a two-arm, randomized, double-blind, placebo-controlled cohort study with 2:1 treatment allocation. Healthy military volunteers in areas along the Thai-Cambodian border where there is a high risk of malaria were administered two consecutive daily doses of 180 mg dihydroartemisinin and 1,440 mg p</pubmed_abstract><journal>Antimicrobial agents and chemotherapy</journal><pagination>6056-67</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4187937</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Randomized, double-blind, placebo-controlled clinical trial of a two-day regimen of dihydroartemisinin-piperaquine for malaria prevention halted for concern over prolonged corrected QT interval.</pubmed_title><pmcid>PMC4187937</pmcid><pubmed_authors>Sriwichai S</pubmed_authors><pubmed_authors>Lanteri C</pubmed_authors><pubmed_authors>Chour CM</pubmed_authors><pubmed_authors>Vanachayangkul P</pubmed_authors><pubmed_authors>Tang D</pubmed_authors><pubmed_authors>Se Y</pubmed_authors><pubmed_authors>Prom S</pubmed_authors><pubmed_authors>So M</pubmed_authors><pubmed_authors>Siripokasupkul R</pubmed_authors><pubmed_authors>Sea D</pubmed_authors><pubmed_authors>Saunders D</pubmed_authors><pubmed_authors>Soh E</pubmed_authors><pubmed_authors>Teja-Isavadharm P</pubmed_authors><pubmed_authors>Manning J</pubmed_authors><pubmed_authors>Kaewkungwal J</pubmed_authors><pubmed_authors>Somethy S</pubmed_authors><pubmed_authors>Spring M</pubmed_authors><pubmed_authors>Cantilena L</pubmed_authors><pubmed_authors>Chann S</pubmed_authors><pubmed_authors>Lon C</pubmed_authors><pubmed_authors>Mitprasat M</pubmed_authors><pubmed_authors>Kuntawunginn W</pubmed_authors><pubmed_authors>Phann ST</pubmed_authors><pubmed_authors>Auayporn M</pubmed_authors><pubmed_authors>Buathong N</pubmed_authors><pubmed_authors>Haigney M</pubmed_authors><pubmed_authors>Timmermans A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Randomized, double-blind, placebo-controlled clinical trial of a two-day regimen of dihydroartemisinin-piperaquine for malaria prevention halted for concern over prolonged corrected QT interval.</name><description>Dihydroartemisinin-piperaquine, the current first-line drug for uncomplicated malaria caused by Plasmodium falciparum and Plasmodium vivax in Cambodia, was previously shown to be of benefit as malaria chemoprophylaxis when administered as a monthly 3-day regimen. We sought to evaluate the protective efficacy of a compressed monthly 2-day treatment course in the Royal Cambodian Armed Forces. The safety and efficacy of a monthly 2-day dosing regimen of dihydroartemisinin-piperaquine were evaluated in a two-arm, randomized, double-blind, placebo-controlled cohort study with 2:1 treatment allocation. Healthy military volunteers in areas along the Thai-Cambodian border where there is a high risk of malaria were administered two consecutive daily doses of 180 mg dihydroartemisinin and 1,440 mg p</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Oct</publication><modification>2026-04-29T19:37:53.872Z</modification><creation>2019-03-26T23:50:36Z</creation></dates><accession>S-EPMC4187937</accession><cross_references><pubmed>25092702</pubmed><doi>10.1128/aac.02667-14</doi><doi>10.1128/AAC.02667-14</doi></cross_references></HashMap>