Long‐Acting Therapeutics in Pediatric Health: Bridging Innovation and Access

Children have distinct therapeutic needs arising from age-dependent physiology, disease epidemiology, formulation requirements, dosing considerations, and safety vulnerabilities. Despite substantial reductions in childhood mortality over the past three decades, nearly 5 million children under five died in 2023, with infectious diseases continuing to contribute substantially to preventable morbidity and mortality. Long-acting therapeutics (LATs) may help address selected pediatric health priorities by sustaining therapeutic or prophylactic exposure, reducing dosing frequency, and improving adherence and implementation feasibility. This review synthesizes insights from the pediatric health session of the Community of Practice for Long-acting Therapeutics for Maternal and Paediatric Health workshop. The session considered priority pediatric conditions in which existing or emerging LAT approaches could have clinical or public health impact, including lower respiratory tract infections, malaria, tuberculosis, HIV, and syphilis, as well as selected noninfectious indications such as childhood cancer and growth hormone deficiency. We then examine clinical pharmacology and safety considerations central to pediatric LAT development, including developmental pharmacokinetics, absorption-limited disposition and flip-flop kinetics, pharmacokinetic tailing, dose selection, model-informed development, and injection-site tolerability. The review also discusses long-acting technology platforms with potential pediatric applications, route-of-administration considerations, excipient safety, formulation design, acceptability, and implementation challenges. Finally, we propose recommendations to support pediatric LAT development, including early integration of developmental pharmacology, age- and weight-informed dosing, standardized acceptability assessment, product-attribute frameworks, regulatory engagement, and equitable access planning. Realizing the potential of LATs for children will require coordinated, child-centered, and equity-driven approaches that address evidence generation, formulation suitability, implementation context, and affordability from the outset.

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Publication Details

Journal
Clinical Pharmacology & Therapeutics
Published
2026-08-28
DOI
https://doi.org/10.1002/cpt.70458
Primary Topic
Pharmaceutical studies and practices
Type
article
Field-Weighted Citation Impact
0.00

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article

Long‐Acting Therapeutics in Pediatric Health: Bridging Innovation and Access

Daniel B. Hawcutt, Adeniyi Olagunju, Edmund V. Capparelli, Moherndran Archary et al.
Clinical Pharmacology & Therapeutics
Pharmaceutical studies and practices
article

Long‐Acting Therapeutics in Pediatric Health: Bridging Innovation and Access

Daniel B. Hawcutt, Adeniyi Olagunju, Edmund V. Capparelli, Moherndran Archary, Prajith Venkatasubramanian, Rachel Daley
article en

Abstract

Children have distinct therapeutic needs arising from age-dependent physiology, disease epidemiology, formulation requirements, dosing considerations, and safety vulnerabilities. Despite substantial reductions in childhood mortality over the past three decades, nearly 5 million children under five died in 2023, with infectious diseases continuing to contribute substantially to preventable morbidity and mortality. Long-acting therapeutics (LATs) may help address selected pediatric health priorities by sustaining therapeutic or prophylactic exposure, reducing dosing frequency, and improving adherence and implementation feasibility. This review synthesizes insights from the pediatric health session of the Community of Practice for Long-acting Therapeutics for Maternal and Paediatric Health workshop. The session considered priority pediatric conditions in which existing or emerging LAT approaches could have clinical or public health impact, including lower respiratory tract infections, malaria, tuberculosis, HIV, and syphilis, as well as selected noninfectious indications such as childhood cancer and growth hormone deficiency. We then examine clinical pharmacology and safety considerations central to pediatric LAT development, including developmental pharmacokinetics, absorption-limited disposition and flip-flop kinetics, pharmacokinetic tailing, dose selection, model-informed development, and injection-site tolerability. The review also discusses long-acting technology platforms with potential pediatric applications, route-of-administration considerations, excipient safety, formulation design, acceptability, and implementation challenges. Finally, we propose recommendations to support pediatric LAT development, including early integration of developmental pharmacology, age- and weight-informed dosing, standardized acceptability assessment, product-attribute frameworks, regulatory engagement, and equitable access planning. Realizing the potential of LATs for children will require coordinated, child-centered, and equity-driven approaches that address evidence generation, formulation suitability, implementation context, and affordability from the outset.

Clinical Pharmacology & Therapeutics
University of Liverpool (GB), University of California San Diego (US), Rady Children's Hospital-San Diego (US), Liverpool Women's Hospital (GB), Alder Hey Children's NHS Foundation Trust (GB), Africa Health Research Institute (ZA), Centre of Excellence for Long-acting Therapeutics (GB), University of Montana (US)
Wellcome Trust, National Institute for Health and Care Research, National Institutes of Health
Industry, innovation and infrastructure
Openalex Percentile: Top 7%
Pharmaceutical studies and practices
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