Artesunate-Clindamycin versus Quinine-Clindamycin in the Treatment ofPlasmodium falciparum Malaria: A Randomized Controlled Trial
Author(s) -
P. G. Kremsner,
Michael Ramharter,
Sunny Oyakhirome,
P. K. Klouwenberg,
Ayôla Akim Adégnika,
S. T. Agnandji,
Michel A. Missinou,
P.-B. Matsiegui,
Benjamin Mordmüller,
Steffen Borrmann,
J. F. Kun,
B. Lell,
Sanjeev Krishna,
W. Graninger,
S. Issifou
Publication year - 2005
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1086/430309
Subject(s) - artesunate , medicine , clindamycin , tolerability , artemisinin , quinine , malaria , plasmodium falciparum , population , regimen , adverse effect , pharmacology , antibiotics , immunology , biology , microbiology and biotechnology , environmental health
Artemisinin-based drug combinations are the mainstay in the fight against drug-resistant malaria in Africa. Currently available antimalarial drug combinations that include artemisinins are pharmacokinetically unmatched and are therefore potentially increasing the risk of selection of resistant mutants in areas in which the rate of transmission of malaria is high. We tested the potential value of artemisinin-based combination therapy with a short elimination half-life for the treatment of uncomplicated Plasmodium falciparum malaria in sub-Saharan Africa.
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