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Study details
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A Study to Learn More About How Risankizumab Works in Young Participants With Ulcerative Colitis

AbbVie
NCT IDNCT07071519ClinicalTrials.gov data as of Apr 2026
Phase

Phase 3

Target enrollment

120

Study length

about 9 years

Ages

2–17

Locations

6 sites in AZ, FL, GA +3

About this study

Researchers are testing how well a treatment called risankizumab works in children with ulcerative colitis. The trial will also look at how safe and effective the treatment is, as well as any side effects that may occur. Around 120 children with UC will be enrolled at sites around the world.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Risankizumab
PhasePhase 3
DrugRisankizumab
Primary goalNumber of Participants With Adverse Events

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low8%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

risankizumab

Endpoints

Primary: Number of Participants With Adverse Events, PK Lead-In Cohort 1: Area Under the Serum Concentration-Time Curve Over the Dosing Interval (AUCtau), PK Lead-In Cohort 1: Maximum Observed Serum Concentration (Cmax), PK Lead-In Cohort 1: Time to Maximum Serum Concentration (Tmax), PK Lead-In Cohort 2: Area Under the Serum Concentration-Time Curve Over the Dosing Interval (AUCtau), PK Lead-In Cohort 2: Maximum Observed Serum Concentration (Cmax), PK Lead-In Cohort 2: Time to Maximum Serum Concentration (Tmax)

Secondary: PK Lead-In Cohort 1: Ability to discontinue corticosteroids prior to Week 64 (at least 90 days without corticosteroid exposure) and achievement of clinical remission per mMS among Week 12 responders per mMS, PK Lead-In Cohort 1: Achievement of clinical remission per mMS, PK Lead-In Cohort 1: Achievement of clinical remission per mMS among Week 12 responders per mMS, PK Lead-In Cohort 1: Achievement of clinical response per mMS, PK Lead-In Cohort 1: Achievement of clinical response per mMS among Week 12 responders per mMS, PK Lead-In Cohort 1: Achievement of endoscopic improvement, PK Lead-In Cohort 1: Achievement of endoscopic improvement among Week 12 responders per mMS, PK Lead-In Cohort 1: Symptomatic response per partial mMS

Body systems

Gastroenterology