Related Experiment Video
Updated: May 15, 2026

An Affordable HIV-1 Drug Resistance Monitoring Method for Resource Limited Settings
Published on: March 30, 2014
Individual patient data meta-analysis: a cost-effective and efficient tool to advance paediatric research in low- and
Frederick McElwee1, Andrew Farlow2, Philippe J Guerin3,4,5
1Economics of Population Health Research Centre, University of Oxford, Oxford, England, UK frederick.mcelwee@dph.ox.ac.uk.
Insights
Paediatric clinical research in low- and middle-income countries (LMICs) is insufficient due to commercial barriers. Individual patient data meta-analysis (IPD-MA) offers a cost-effective solution to bridge this gap, as demonstrated in antimalarial drug studies.
Area of Science:
- Global Health
- Clinical Research
- Pharmacovigilance
Background:
- Significant deficit in pediatric clinical research in low- and middle-income countries (LMICs) compared to disease burden.
- Commercial barriers including lack of market protections and pricing issues hinder industry-funded pediatric research and access to therapeutics in LMICs.
Purpose of the Study:
- To address the research gap in pediatric clinical research in LMICs.
- To explore the potential of individual patient data meta-analysis (IPD-MA) as a cost-effective research tool.
Main Methods:
- Leveraging existing clinical trials through data sharing.
- Utilizing individual patient data meta-analysis (IPD-MA).
- Case study of recent IPD-MAs on pediatric antimalarial drug safety and efficacy.
Main Results:
- Demonstrated feasibility of IPD-MA for pediatric research in LMICs.
- Successful application of IPD-MA in antimalarial drug safety and efficacy studies.
- Highlighted the efficiency and cost-effectiveness of data sharing for research.
Conclusions:
- IPD-MA is a viable and efficient strategy to bridge the pediatric research gap in LMICs.
- Data sharing initiatives like WWARN and IDDO are crucial for enabling IPD-MA.
- Further adoption of IPD-MA can improve pediatric health outcomes in resource-limited settings.
Abstract:
There is a deficit between existing levels of paediatric clinical research in low- and middle-income countries (LMICs) and what is warranted based on the disease burden in children in these countries. Lack of market protections, low ability to pay and cost-based pricing are key commercial barriers to industry-funded paediatric research and access to paediatric formulations of therapeutics in LMICs. Individual patient data meta-analysis (IPD-MA) taking advantage of existing clinical trials, enabled by data sharing, is one potential tool to bridge the research gap in a cost-effective and efficient way. Recent IPD-MAs of paediatric antimalarial drug safety and efficacy enabled by the WorldWide Antimalarial Resistance Network (WWARN), part of the Infectious Diseases Data Observatory (IDDO), demonstrate the feasibility of this approach.
Related Concept Videos
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Analysis of Population Pharmacokinetic Data
Pharmacokinetics in Pediatric Patients: Drug Excretion
Pharmacokinetics in Pediatric Patients: Drug Distribution
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption
Dosage Regimens: Partial Pharmacokinetic Parameters
