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Efficacy of upadacitinib induction for pediatric inflammatory bowel disease
Evan Greenhall1, Nina Gautam2, Paula Prieto-Jimenez1
1Division of Pediatric Gastroenterology Phoenix Children's Hospital Phoenix Arizona USA.
Insights
Pediatric inflammatory bowel disease patients on upadacitinib experienced high relapse rates after dose reduction. Many regained response by increasing the dose, suggesting individualized maintenance strategies are crucial.
Area of Science:
- Pediatric Gastroenterology
- Immunology
- Pharmacology
Background:
- Upadacitinib, a JAK inhibitor, is approved for adult Crohn's disease and ulcerative colitis.
- Efficacy in pediatric inflammatory bowel disease (IBD) is not well-established.
- Early reports suggest potential benefits but also relapse risks with dose reduction.
Purpose of the Study:
- To evaluate the sustained efficacy of upadacitinib in pediatric IBD patients.
- To assess relapse rates during transition from induction to maintenance dosing.
- To determine the response to dose adjustments in pediatric IBD.
Main Methods:
- A case series of 16 pediatric IBD patients treated with upadacitinib.
- Analysis focused on 8 patients transitioning from 45 mg daily induction to 30 or 15 mg daily maintenance.
- Relapse rates and response to dose adjustments were assessed.
Main Results:
- Seven of 16 patients (43.8%) lost response after transitioning to maintenance dosing.
- Median time to relapse was 81.5 days.
- Six of these 7 patients (85.7%) regained response upon dose increase to induction levels.
Conclusions:
- Pediatric IBD patients may require higher maintenance doses or individualized upadacitinib dosing.
- High relapse rates necessitate close monitoring and tailored treatment strategies.
- Pharmacokinetic considerations may influence optimal dosing in this population.
Objectives:
Upadacitinib, a second-generation Janus kinase (JAK) inhibitor, is approved for moderate to severe Crohn's disease (CD) and ulcerative colitis (UC) in adults. Its efficacy in pediatric patients remains unclear, though early reports suggest benefits in refractory inflammatory bowel disease (IBD). However, data indicate potential relapse after dose reduction. This study evaluates upadacitinib's sustained efficacy in pediatric IBD, particularly when transitioning from induction to maintenance dosing.
Methods:
We conducted a case series of 16 pediatric patients (mean age 16.1 years) treated with upadacitinib for refractory IBD between 2023 and 2024. Treatment responses were analyzed in 8 patients who completed induction (45 mg daily) and transitioned to maintenance dosing (30 or 15 mg daily based on provider preference). Relapse rates and responses to dose adjustments were assessed.
Results:
Among the 16 patients, 8 had UC, 7 had CD, and 1 had IBD-unclassified. Seven (43.8%; 95% confidence interval [CI], 19.4%-68.1%) lost response after transitioning to maintenance, with a median time to relapse of 81.5 days. Of these, 6 (85.7%; 95% CI, 42%-99%) regained response after increasing the dose back to induction dosing.
Conclusion:
Our findings suggest that pediatric patients may require longer induction, higher maintenance doses, or individualized dosing due to pharmacokinetics. Given the high relapse rate in our small cohort, close monitoring and tailored treatment strategies are essential.
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