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Study identifier: NCT05552287 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Pharmacokinetic Infliximab Data in Pediatric Crohn's Disease

Condition: Crohn Disease · Child, Only · Biologic; Inadequate  ·  Sponsor: Erasmus Medical Center

PhasePhase 4
Planned participants50
Who can joinAll sexes, 1 Year to 15 Years
Healthy volunteersNo

About this study

Rationale: Crohn's disease (CD) is a chronic, debilitating inflammatory bowel disease (IBD) which is diagnosed during childhood in up to one in ten patients. The use of anti-tumor necrosis factor (TNF)-α agents has significantly ameliorated CD management. Infliximab (IFX) is the first anti-TNF-α agent registered for pediatric CD. The current dosing recommendation of IFX is extrapolated from adult studies, and it is a weight-based dose (5 mg/kg) delivered during induction (infusion at weeks 0, 2, and 6) and maintenance (every 8 weeks). However, pediatric patients have a 25-40% lower drug exposure compared to adults, particularly children under 10 years of age, resulting in diminished efficacy and an increased risk of developing a complicated disease course. The investigators hypothesize that an intensified IFX induction scheme (instead of the current dosing recommendation) is more effective in the treatment of pediatric CD patients. Objective: The primary study objective of our study is to assess the efficacy of an IFX intensified induction scheme vs. a standard dosing schedule in improving drug exposure without treatment escalation in pediatric CD patients. Secondary objectives are clinical and biochemical remission without treatment escalation, development of antibodies to IFX (ATI) and adverse reactions. Study design: An international, multicenter, prospective, open-label trial. Study population: Anti-TNF-α naïve children (age 1-15 years) with CD and an indication to star…

This description comes directly from the study's public registry record.

Talk to the study team

Lissy de Ridder, PhD  ·  0107036076  ·  l.deridder@erasmusmc.nl

Always discuss trial participation with your own doctor first.

Locations (1)

Erasmus Medical CenterRotterdam, NetherlandsRecruiting

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Source record: clinicaltrials.gov/study/NCT05552287