Short-Course Regimens of Artesunate-Fosmidomycin in Treatment of Uncomplicated Plasmodium falciparum Malaria

Author:

Borrmann Steffen12,Adegnika Ayola A.12,Moussavou Félicien13,Oyakhirome Sunny1,Esser Gilbert12,Matsiegui Pierre-Blaise12,Ramharter Michael4,Lundgren Ingrid15,Kombila Maryvonne3,Issifou Saadou12,Hutchinson David6,Wiesner Jochen7,Jomaa Hassan7,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. Département de Parasitologie-Mycologie, Faculté de Médecine, Université des Sciences de la Santé, Libreville, Gabon

4. Division of Infectious Diseases, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria

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

6. Jomaa Pharma GmbH, Hamburg, Germany

7. Institute of Biochemistry, University of Giessen, Giessen, Germany

Abstract

ABSTRACT Fosmidomycin is effective against malaria, but it needs to be given for ≥4 days when used alone. We conducted a study of 50 children with Plasmodium falciparum malaria to evaluate the safety and efficacy of consecutively shortened regimens of artesunate-fosmidomycin (1 to 2 mg/kg of body weight and 30 mg/kg of body weight, respectively; doses given every 12 hours). All dosing regimens were well tolerated. Artesunate-fosmidomycin acted rapidly, resulting in consolidated geometric mean parasite and fever clearance times of 24 h and 15 h, respectively. Treatment regimens of ≥2 days led to cure ratios of 100% by day 14 (39/39; 95% confidence interval [95% CI], 91% to 100%). Most importantly, the 3-day regimen achieved 100% cure on day 28 (10/10; 95% CI, 69% to 100%). Treatment with artesunate-fosmidomycin was associated with transient grade I or II neutropenia (absolute neutrophil counts of 750 to 1,200/μl and 400 to 749/μl, respectively) in six or two patients, respectively. Artesunate-fosmidomycin demonstrates the feasibility and potential value of short-course artemisinin-based combination chemotherapy with rapidly eliminated combination partners.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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