Abstract |
This single-arm trial (n = 104) in western Cambodia showed high efficacy for 3-day treatment with pyronaridine-artesunate plus single-dose primaquine in Plasmodium falciparum malaria. Day 42 PCR-adjusted adequate clinical and parasitological response (ACPR) was 98.3% (58/59) (95% confidence interval [CI], 90.9 to 100.0) in Trapeng Chau in Kampong Speu and 100% (41/41) (95% CI, 91.4 to 100) in Veal Veng in Pursat; 80.6% (83/103) of the patients had P. falciparum with drug resistance molecular markers. For Plasmodium vivax malaria, pyronaridine-artesunate day 28 ACPR was 98.3% (59/60) (95% CI, 91.1 to 100) and 100% (60/60) (95% CI, 94.0 to 100), respectively. (This study is registered in the Australian New Zealand Clinical Trials Registry [ANZCTR] under reference no. ACTRN12618001999224.).
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Authors | Rithea Leang, Nimol Khim, Huch Chea, Rekol Huy, Melissa Mairet-Khedim, Denis Mey Bouth, Maria Dorina Bustos, Pascal Ringwald, Benoit Witkowski |
Journal | Antimicrobial agents and chemotherapy
(Antimicrob Agents Chemother)
Vol. 63
Issue 10
(10 2019)
ISSN: 1098-6596 [Electronic] United States |
PMID | 31358594
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
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Copyright | Copyright © 2019 American Society for Microbiology. |
Chemical References |
- Antimalarials
- Naphthyridines
- Artesunate
- Primaquine
- pyronaridine
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Topics |
- Adolescent
- Adult
- Antimalarials
(adverse effects, therapeutic use)
- Artesunate
(adverse effects, therapeutic use)
- Cambodia
- Child
- Drug Resistance
- Female
- Humans
- Malaria
(drug therapy)
- Male
- Middle Aged
- Naphthyridines
(adverse effects, therapeutic use)
- Plasmodium vivax
(drug effects, pathogenicity)
- Primaquine
(adverse effects, therapeutic use)
- Young Adult
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