Abstract

BackgroundThe World Health Organization (WHO) recommends artemisinin combination therapy (ACT) for the treatment of uncomplicated Plasmodium falciparum malaria. The present study investigated the efficacy and safety of fixed dose combination (FDC) of arterolane maleate 37.5 mg and piperaquine phosphate (PQP) 187.5 mg dispersible tablets in paediatric patients aged 6 months to 12 years.MethodsMale and female patients aged 6 months to 12 years who were confirmed cases of P. falciparum mono-infection with fever or documented history of fever in the previous 24 h were included. The patients were administered FDC of arterolane maleate and PQP as single daily doses for three consecutive days based on their age. The primary efficacy outcome was proportion of patients with polymerase chain reaction (PCR)-corrected adequate clinical and parasitological response (ACPR) on day 28. Safety was analysed based on adverse events (AE), laboratory abnormalities and abnormalities on electrocardiograph.ResultsA total of 141 eligible paediatric patients received FDC of arterolane maleate and PQP in a 42-day follow-up study. All the enrolled patients (141) were included in intention to treat (ITT) and safety analyses, and 126 patients were considered in per protocol (PP) population. The PCR-corrected ACPR on day 28 was achieved in all patients (100 %; 95 % CI 97.11–100) included in PP population. The median parasite clearance time (PCT) and fever clearance time (FCT) were 24 h (95 % CI 18.0–24.0) and 10 h (95 % CI 4.0–18.0), respectively. The most frequently reported clinical AE was vomiting. Majority of the AEs were mild to moderate in severity and resolved without sequelae. No patient was discontinued for any QTc (corrected QT interval) prolongation. No deaths or serious AEs were reported during the study.ConclusionThe findings from this study showed that FDC of arterolane maleate and PQP effectively cures P. falciparum malaria and attains acceptable level of cure by day 28 in paediatric patients. The efficacy and safety results observed in children warrants further studies on FDC of arterolane maleate and PQP dispersible tablets.Trial Registration: Clinical Trial Registry India: CTRI/2009/091/000531

Highlights

  • The World Health Organization (WHO) recommends artemisinin combination therapy (ACT) for the treatment of uncomplicated Plasmodium falciparum malaria

  • All the secondary endpoint (ACPR uncorrected at day 28, Adequate clinical and parasitological response (ACPR) uncorrected/corrected at day 42, parasite clearance time (PCT), and fever clearance time (FCT)) analyses were done on intention to treat (ITT) population, which included all patients who received at least one dose of study medication

  • Demographics and baseline characteristics A total of 141 patients were enrolled in the study to receive fixed dose combination (FDC) of arterolane maleate and piperaquine phosphate dispersible tablets

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Summary

Introduction

The World Health Organization (WHO) recommends artemisinin combination therapy (ACT) for the treatment of uncomplicated Plasmodium falciparum malaria. Artemisinin combination therapy (ACT) is the WHO-recommended first-line treatment for uncomplicated falciparum malaria in all endemic regions [2, 3]. Artemisinin derivatives are derived from plant source, so harvesting and extraction costs remain variable. Piperaquine phosphate is a proven effective and well-tolerated anti-malarial drug. The tolerability, efficacy and pharmacokinetic profile and low cost of piperaquine phosphate make it a promising partner drug for use as part of ACT [4, 7, 8]. Arterolane maleate has been combined with piperaquine phosphate (long-acting anti-malarial) in a fixed dose combination

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