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Fosmidomycin plus clindamycin for treatment of pediatric patients aged 1 to 14 years with Plasmodium falciparum malaria
Authors:Borrmann Steffen  Lundgren Ingrid  Oyakhirome Sunny  Impouma Bénido  Matsiegui Pierre-Blaise  Adegnika Ayola A  Issifou Saadou  Kun Jürgen F J  Hutchinson David  Wiesner Jochen  Jomaa Hassan  Kremsner Peter G
Affiliation:Steffen Borrmann, Ingrid Lundgren, Sunny Oyakhirome, Bénido Impouma, Pierre-Blaise Matsiegui, Ayola A. Adegnika, Saadou Issifou, Jürgen F. J. Kun, David Hutchinson, Jochen Wiesner, Hassan Jomaa, and Peter G. Kremsner
Abstract:Fosmidomycin plus clindamycin was shown to be efficacious in the treatment of uncomplicated Plasmodium falciparum malaria in a small cohort of pediatric patients aged 7 to 14 years, but more data, including data on younger children with less antiparasitic immunity, are needed to determine the potential value of this new antimalarial combination. We conducted a single-arm study to improve the precision of efficacy estimates for an oral 3-day fixed-ratio combination of fosmidomycin and clindamycin at 30 and 10 mg/kg of body weight, respectively, every 12 hours for the treatment of uncomplicated P. falciparum malaria in 51 pediatric outpatients aged 1 to 14 years. Fosmidomycin plus clindamycin was generally well tolerated, but relatively high rates of treatment-associated neutropenia (8/51 [16%]) and falls of hemoglobin concentrations of ≥2 g/dl (7/51 [14%]) are of concern. Asexual parasites and fever were cleared within median periods of 42 h and 38 h, respectively. All patients who could be evaluated were parasitologically and clinically cured by day 14 (49/49; 95% confidence interval [CI], 93 to 100%). The per-protocol, PCR-adjusted day 28 cure rate was 89% (42/47; 95% CI, 77 to 96%). Efficacy appeared to be significantly reduced in children aged 1 to 2 years, with a day 28 cure rate of only 62% for this small subgroup (5/8). The inadequate efficacy in children of <3 years highlights the need for continued systematic studies of the current dosing regimen, which should include randomized trial designs.
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