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Published on: April 25, 2025
Antiparasitic drugs for paediatrics: systematic review, formulations, pharmacokinetics, safety, efficacy and
Jennifer Keiser1, Katrin Ingram, Jürg Utzinger
1Department of Medical Parasitology and Infection Biology, Swiss Tropical and Public Health Institute, P.O. Box, CH-4002 Basel, Switzerland. jennifer.keiser@unibas.ch
Insights
This review found that antiparasitic drugs, particularly antimalarials, have been studied in children, but more research is needed to ensure their safety and efficacy across all pediatric age groups and for various parasitic infections.
Area of Science:
- Paediatric Pharmacology
- Infectious Diseases
- Drug Development
Background:
- Children represent a vulnerable population disproportionately affected by parasitic diseases.
- Drug efficacy and safety in pediatric populations are influenced by developmental changes.
- There is a need to ensure antiparasitic drugs are adequately studied for pediatric use.
Purpose of the Study:
- To systematically review the extent of research on antiparasitic drugs for pediatric applications.
- To assess the available data on efficacy, safety, and pharmacokinetics of these drugs in children.
- To evaluate drug formulations and inform strategies for preventive chemotherapy in young children.
Main Methods:
- Systematic review of clinical trials and pharmacokinetic studies from PubMed and Cochrane Central Register of Trials.
- Inclusion criteria focused on studies investigating efficacy, safety, and PK parameters of antiparasitic drugs in pediatric populations.
- Data collection covered a period of 10 years and 8 months until August 2010.
Main Results:
- 269 clinical trials and 17 PK studies met the inclusion criteria.
- Antimalarial drugs were the most frequently studied class (82.6%).
- Most trials were conducted in Africa, with children aged 2-11 years being the most studied group. Shortcomings in anthelminthic formulations were identified.
Conclusions:
- While some antiparasitic drugs, notably antimalarials, have undergone pediatric investigation, significant gaps remain.
- Further research, including risk-benefit analyses, is crucial before expanding preventive chemotherapy strategies to younger children.
- Improved drug formulations and targeted research are necessary to optimize antiparasitic treatment in diverse pediatric populations.
Abstract:
Drug development for paediatric applications entails a number of challenges, such as the wide age spectrum covered - from birth to adolescence - and developmental changes in physiology during biological maturation that influence the efficacy and toxicity of drugs. Safe and efficacious antiparasitic drugs for children are of pivotal importance given the large proportion of burden attributable to parasitic diseases in this age group, and growing efforts to administer, as widely as possible, antiparasitic drugs to at-risk populations, such as infants and school-aged children, often without prior diagnosis. The purpose of this review is to investigate whether antiparasitic drugs have been adequately studied for use in paediatrics. We approached this issue through a systematic review using PubMed and the Cochrane Central Register of Trials covering a period of 10 years and 8 months until the end of August 2010 to identify trials that investigated efficacy, safety and pharmacokinetic (PK) parameters of antiparasitic drugs for paediatrics. Overall, 269 clinical drug trials and 17 PK studies met our inclusion criteria. Antimalarial drugs were the most commonly studied medicines (82·6%). Most trials were carried out in Africa and children aged 2-11 years were the age group most often investigated. Additionally, we critically examined available drug formulations for anthelminthics and identified a number of shortcomings that are discussed. Finally, we shed new light on current proposals to expand 'preventive chemotherapy' to preschool-aged children and emphasise that new research, including risk-benefit analyses, are needed before such a strategy can be adopted more widely.
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