Evidence map›Paper›PMID 40820139›Full record

ArticleJournal of clinical pharmacology2025

Recent Utilization of Pediatric Extrapolation and Modeling and Simulation Approaches in Pediatric Drug Development in Japan.

Akinori Nakashima, Akihide Tsujimoto, Masako Saito, Jun Takeda, Makiko Natori, Satoshi Shoji

Abstract read
In one paragraph

Article in Journal of clinical pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Akinori NakashimaJapan Pharmaceutical Manufacturers Association Clinical Evaluation Expert Committee, Drug Evaluation Committee, Tokyo, Japan.
Akihide TsujimotoJapan Pharmaceutical Manufacturers Association Clinical Evaluation Expert Committee, Drug Evaluation Committee, Tokyo, Japan.ORCID 0000-0002-1539-6306
Masako SaitoJapan Pharmaceutical Manufacturers Association Clinical Evaluation Expert Committee, Drug Evaluation Committee, Tokyo, Japan.
Jun TakedaJapan Pharmaceutical Manufacturers Association Clinical Evaluation Expert Committee, Drug Evaluation Committee, Tokyo, Japan.
Makiko NatoriJapan Pharmaceutical Manufacturers Association Clinical Evaluation Expert Committee, Drug Evaluation Committee, Tokyo, Japan.
Satoshi ShojiJapan Pharmaceutical Manufacturers Association Clinical Evaluation Expert Committee, Drug Evaluation Committee, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In Japan, the percentage of approved drugs with pediatric indications increased to 30% in 2010-2015, but no further increase was observed through 2020. The Ministry of Health, Labor, and Welfare in Japan presented draft future directions to promote pediatric drug development, where the modeling and simulation (M&S) approach was introduced as a tool to support efficacy and safety, utilizing existing data when building a flexible data package for pediatric drug approval. M&S is considered a powerful scientific tool in pediatric drug development using the pediatric extrapolation approach. We examined approval application data packages for pediatric drugs approved in Japan from January 2019 to March 2023, where 95 drug products were identified as pediatric drugs for this survey. Drugs with complete, partial, or no extrapolation accounted for 43.2%, 30.5%, and 26.3% of the total drugs, respectively. M&S was widely used as the major rationale in dose selection for pediatric clinical trials and/or the recommended dosing regimen in drug approval applications for the pediatric population (60.0%). Further use of existing data with extrapolation strategies may lead to the development of flexible and efficient data packages for pediatric drug approval. Since safety profiles may be different between pediatric and adult populations due to age-related factors, pediatric developmental safety should be incorporated into M&S in future assessments. The pharmaceutical industry, regulatory authorities, and academia need to discuss development strategies from an early stage and share lessons learned, thereby facilitating further discussions on efficient pediatric drug development and delivering drugs for children without delay in Japan.

Indexed as

Drug DevelopmentModels, BiologicalChildComputer SimulationDrug ApprovalHumansJapanPediatricsclinical data packageclinical pharmacologydrug developmentextrapolationmodel informed drug developmentmodeling and simulationpediatricspharmaceutical R&Dpharmacometrics

Identifiers

PMID40820139
PMCPMC12649297

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