Innovations in Pediatric Therapeutics Development: Principles for the Use of Bridging Biomarkers in Pediatric Extrapolation

Even with recent substantive improvements in health care in pediatric populations, considerable need remains for additional safe and effective interventions for the prevention and treatment of diseases in children. The approval of prescription drugs and biological products for use in pediatric setti...

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Veröffentlicht in:Therapeutic innovation & regulatory science 2023-01, Vol.57 (1), p.109-120
Hauptverfasser: Fleming, Thomas R., Garnett, Christine E., Conklin, Laurie S., Corriol-Rohou, Solange, Hariharan, Sudharshan, Hsu, Daphne, Mueller-Velten, Guenther, Mulugeta, Yeruk, Portman, Ronald, Rothmann, Mark D., Stockbridge, Norman L., Wandel, Simon, Zhang, Jialu, Yao, Lynne
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container_end_page 120
container_issue 1
container_start_page 109
container_title Therapeutic innovation & regulatory science
container_volume 57
creator Fleming, Thomas R.
Garnett, Christine E.
Conklin, Laurie S.
Corriol-Rohou, Solange
Hariharan, Sudharshan
Hsu, Daphne
Mueller-Velten, Guenther
Mulugeta, Yeruk
Portman, Ronald
Rothmann, Mark D.
Stockbridge, Norman L.
Wandel, Simon
Zhang, Jialu
Yao, Lynne
description Even with recent substantive improvements in health care in pediatric populations, considerable need remains for additional safe and effective interventions for the prevention and treatment of diseases in children. The approval of prescription drugs and biological products for use in pediatric settings, as in adults, requires demonstration of substantial evidence of effectiveness and favorable benefit-to-risk. For diseases primarily affecting children, such evidence predominantly would be obtained in the pediatric setting. However, for conditions affecting both adults and children, pediatric extrapolation uses scientific evidence in adults to enable more efficiently obtaining a reliable evaluation of an intervention’s effects in pediatric populations. Bridging biomarkers potentially have an integral role in pediatric extrapolation. In a setting where an intervention reliably has been established to be safe and effective in adults, and where there is substantive evidence that disease processes in pediatric and adult settings are biologically similar, a ‘bridging biomarker’ should satisfy three additional criteria: effects on the bridging biomarker should capture effects on the principal causal pathway through which the disease process meaningfully influences ‘feels, functions, survives’ measures; secondly, the experimental intervention should not have important unintended effects on ‘feels, functions, survives’ measures not captured by the bridging biomarker; and thirdly, in statistical analyses in adults, the intervention’s net effect on ‘feels, functions, survives’ measures should be consistent with what would be predicted by its level of effect on the bridging biomarker. A validated bridging biomarker has considerable potential utility, since an intervention’s efficacy could be extrapolated from adult to pediatric populations if evidence in children establishes the intervention not only to be safe but also to have substantive effects on that bridging biomarker. Proper use of bridging biomarkers could increase availability of reliably evaluated therapies approved for use in pediatric settings, enabling children and their caregivers to make informed choices about health care.
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subjects Adult
Adults
Biomarkers
Caregivers
Child
Children
Drug development
Drug Safety and Pharmacovigilance
Evaluation
Extrapolation
Health care
Health risks
Humans
Intervention
Medical innovations
Medical treatment
Medicine
Original Research
Pediatrics
Pharmacotherapy
Pharmacy
Populations
Risk Assessment
Statistical analysis
Survival
title Innovations in Pediatric Therapeutics Development: Principles for the Use of Bridging Biomarkers in Pediatric Extrapolation
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