Evidence map›Paper›PMID 42584807›Full record

ArticleJournal of clinical pharmacology2026

PBPK Modeling of Esomeprazole to Support Adolescent Pharmacokinetic Extrapolation and Label Extension in Chinese Patients With Gastroesophageal Reflux Disease (GERD).

Yuwen Jin, Junjie Ding, Xiaohan Hua, Wei Duan, Mo Chen, Zhaohui Zhou, Ramesh V Pandherpur, Jin Dong, Sharma Pradeep, Peiming Ma and 2 more

Abstract read
In one paragraph

Article in Journal of clinical pharmacology, 2026. 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

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Yuwen JinClinical Pharmacology, R&D China, AstraZeneca, Shanghai, China.ORCID https://orcid.org/0009-0003-0977-6921
Junjie DingClinical Pharmacology, R&D China, AstraZeneca, Shanghai, China.
Xiaohan HuaRespiratory & Immunology, R&D China, AstraZeneca, Shanghai, China.
Wei DuanBiometrics and Data Science, R&D China, AstraZeneca, Shanghai, China.
Mo ChenClinical Safety, R&D China, AstraZeneca, Shanghai, China.
Zhaohui ZhouRespiratory & Immunology, R&D China, AstraZeneca, Shanghai, China.
Ramesh V PandherpurClinical Development, BioPharmaceuticals R&D, AstraZeneca, Bengaluru, India.ORCID https://orcid.org/0009-0004-8716-707X
Jin DongClinical Pharmacology & Quantitative Pharmacology, Clinical Pharmacology and Safety Sciences, R&D, AstraZeneca, Gaithersburg, Maryland, USA.ORCID https://orcid.org/0000-0002-3317-0386
Sharma PradeepClinical Pharmacology & Quantitative Pharmacology, Clinical Pharmacology and Safety Sciences, R&D, AstraZeneca, Cambridge, UK.ORCID https://orcid.org/0000-0003-3415-8917
Peiming MaClinical Pharmacology, R&D China, AstraZeneca, Shanghai, China.ORCID https://orcid.org/0000-0003-0246-3132
Weifeng TangClinical Pharmacology & Quantitative Pharmacology, Clinical Pharmacology and Safety Sciences, R&D, AstraZeneca, Gaithersburg, Maryland, USA.ORCID https://orcid.org/0000-0002-8261-8116
Diansong ZhouClinical Pharmacology & Quantitative Pharmacology, Clinical Pharmacology and Safety Sciences, R&D, AstraZeneca, Waltham, Massachusetts, USA.ORCID https://orcid.org/0000-0002-2673-1069

Funding

AstraZeneca
6 · The paper itself

Abstract

Esomeprazole, a proton pump inhibitor (PPI), is widely approved for gastroesophageal reflux disease (GERD) in adults and pediatrics globally, but prior to December 2022, its oral tablets (20 and 40 mg) were approved only for adults in China. To address unmet needs in Chinese adolescents aged 12-17 years, physiologically based pharmacokinetic (PBPK) modeling was employed to extrapolate data and support label extension, leveraging similarities in GERD pathophysiology and PK/PD relationships across ages and ethnicities. A PBPK model was developed for esomeprazole to capture the enteric-coated formulation's pharmacokinetics. The model was validated against clinical PK studies in Caucasian, Japanese, and Chinese adults and/or adolescents, demonstrating good predictions of concentration-time profiles and area under the curve (AUC) for CYP2C19-specific genotypes as well as overall populations across these ethnic groups. All predicted-to-observed ratios for AUC fell within 0.5- to 2.0-fold, with 14 out of 18 predictions within the 0.67- to 1.5-fold. This robust validation enabled the model's application to predict PK in Chinese adolescents. PBPK predictions for Chinese adolescents indicated that steady-state AUC for 20- and 40-mg doses was comparable to that in Japanese adolescents and slightly higher than in Caucasian adolescents. By integrating an established PK/PD relationship between AUC and the percentage of time with intragastric pH >4, once-daily doses of 20 or 40 mg were justified, achieving adequate acid suppression with a favorable safety profile. This PBPK-informed extrapolation was accepted by China's National Medical Products Administration (NMPA), enabling GERD indication extension to adolescents.

Indexed as

EsomeprazoleGastroesophageal RefluxModels, BiologicalProton Pump InhibitorsAdolescentArea Under CurveChildChinaCytochrome P-450 CYP2C19East Asian PeopleFemaleGenotypeHumansMaleTablets, Enteric-CoatedWhite PeopleCYP2C19 protein, humanCytochrome P-450 CYP2C19EsomeprazoleProton Pump InhibitorsTablets, Enteric-CoatedCYP2C19 polymorphismsesomeprazolePBPKpediatric extrapolation

Identifiers

PMID42584807
PMCPMC13464514

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.