Development of Pediatric Dosing for Mepolizumab in Severe Asthma Based on Extrapolation of Data From Adult Patients and a Phase II Open‐Label Pediatric Trial.

The benefit–risk profile of mepolizumab in severe asthma was established through clinical trials in adults, leading to EU and US approvals in 2015. To support a pediatric indication (≥6 years), an extrapolation approach was implemented. This extrapolation and its validation were informed by data fro...

Descripción completa

Detalles Bibliográficos
Publicado en:Journal of Clinical Pharmacology Vol. 66; no. 2; pp. 1 - 11
Autores principales: Gupta, Atul, Pouliquen, Isabelle J., Phipatanakul, Wanda, Austin, Daren, Whelan, Glenn, Price, Robert G., Finney‐Hayward, Tricia, Derey, Sabine, Steinfeld, Jonathan
Formato: research tables/charts Journal Article
Publicado: Wiley-Blackwell Feb2026
Acceso en línea:Ver este registro en EBSCOhost
fields @attributes:
  recordID: 1
pdfLink:
plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=194233221&site=ehost-live
header:
  @attributes:
    shortDbName: ccm
    uiTerm: 194233221
    longDbName: CINAHL Complete
    uiTag: AN
  controlInfo:
    bkinfo:
    dissinfo:
    jinfo:
      jid:
        00912700
        5WH
      jtl: Journal of Clinical Pharmacology
      issn: 00912700
      maglogo: Y
    pubinfo:
      dt: Feb2026
      vid: 66
      iid: 2
      pid: 480
      pub: Wiley-Blackwell
      place: Malden, Massachusetts
    artinfo:
      ui:
        194233221
        194233221
        194233221
        10.1002/jcph.70155
        194233221
      ppf: 1
      ppct: 10
      formats:
      tig:
        atl: Development of Pediatric Dosing for Mepolizumab in Severe Asthma Based on Extrapolation of Data From Adult Patients and a Phase II Open‐Label Pediatric Trial.
      aug:
        au:
          Gupta, Atul
          Pouliquen, Isabelle J.
          Phipatanakul, Wanda
          Austin, Daren
          Whelan, Glenn
          Price, Robert G.
          Finney‐Hayward, Tricia
          Derey, Sabine
          Steinfeld, Jonathan
        affil: Paediatric Respiratory Department, King's College Hospital, Department of Women and Children's Health, London, UK
      sug:
        subj:
          Antibodies, Monoclonal Administration and Dosage
          Severity of Illness
          Asthma Drug Therapy
          Treatment Outcomes
          Antibodies, Monoclonal Pharmacokinetics
          Antibodies, Monoclonal Pharmacodynamics
          Child
          Eosinophilic Esophagitis Drug Therapy
          Eosinophils
          Body Weight
          Disease Exacerbation
          Patient Safety
          Adult
          Middle Age
          Aged
          Aged, 80 and Over
          Adolescence
          Drug Efficacy
          Dose-Response Relationship, Drug
          Human
          Child: 6-12 years
          Adult: 19-44 years
          Middle Aged: 45-64 years
          Aged: 65+ years
          Aged, 80 & over
          Adolescent: 13-18 years
      ab: The benefit–risk profile of mepolizumab in severe asthma was established through clinical trials in adults, leading to EU and US approvals in 2015. To support a pediatric indication (≥6 years), an extrapolation approach was implemented. This extrapolation and its validation were informed by data from Phase III trials in adults (N = 1841) and adolescents aged 12‐17 years (N = 37) with severe asthma, an open‐label trial in children aged 6‐11 years (N = 36), and a trial in children aged 2‐11 years (N = 32) and adolescents aged 12‐17 years (N = 27) with eosinophilic esophagitis. Population pharmacokinetic and pharmacokinetic/pharmacodynamic meta‐analyses demonstrated consistent mepolizumab pharmacokinetic and blood eosinophil reduction across age groups and diseases, with bodyweight the only covariate of exposure and absolute bioavailability also a covariate in children aged 6‐11 years. Baseline blood eosinophil count and disease type were the only covariates of response. In severe asthma, mepolizumab reduced the annualized rate of clinically significant exacerbations by 40% in adolescents and 54% in adults versus placebo. Bootstrap resampling and Bayesian analyses supported similar efficacy between adolescents and adults, and responses in children aged 6‐11 years were consistent with older groups. Safety evaluations revealed no unique safety concerns in pediatric patients with severe asthma. This extrapolation strategy, implemented as an innovative approach to pediatric clinical development of mepolizumab in severe asthma, was validated and provided the scientific basis for dosing recommendations and for EU regulatory approval in patients aged ≥6 years in 2018.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
    refInfo:
    holdings:
      @attributes:
        islocal: N