Fosmidomycin plus Clindamycin for Treatment of Pediatric Patients Aged 1 to 14 Years with Plasmodium falciparum Malaria

Author:

Borrmann Steffen123,Lundgren Ingrid14,Oyakhirome Sunny1,Impouma Bénido1,Matsiegui Pierre-Blaise12,Adegnika Ayola A.12,Issifou Saadou12,Kun Jürgen F. J.2,Hutchinson David5,Wiesner Jochen6,Jomaa Hassan6,Kremsner Peter G.12

Affiliation:

1. Medical Research Unit, Albert Schweitzer Hospital, Lambaréné, Gabon

2. Department of Parasitology, Institute of Tropical Medicine, University of Tübingen, Tübingen, Germany

3. Otto Meyerhof Centre, Heidelberg University School of Medicine, Heidelberg, Germany

4. Mayo Medical School, Mayo Clinic, Rochester, Minnesota

5. Jomaa Pharma GmbH, Hamburg, Germany

6. Institut für Klinische Chemie und Pathobiochemie, Labor Jomaa, Universitätsklinikum Giessen und Marburg, Marburg, Germany

Abstract

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.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference32 articles.

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