← Eichor
Study identifier: NCT06100744 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study to Assess Adverse Events, Change in Disease Activity, and How the Drug Moves Through the Body in Children With Juvenile Psoriatic Arthritis (jPsA) Receiving Subcutaneously Injected Risankizumab or Adalimumab

Condition: Juvenile Psoriatic Arthritis  ·  Sponsor: AbbVie

PhasePhase 3
Planned participants40
Who can joinAll sexes, 5 Years to 17 Years
Healthy volunteersNo

About this study

Psoriatic arthritis (PsA) is a type of arthritis that happens when the body's immune system attacks healthy cells and tissues causing joint pain, stiffness, and swelling. Symptoms can get worse and go away for periods of time. PsA that begins before a patient's 16th birthday is called juvenile PsA (jPsA).This study will evaluate how safe risankizumab is for the treatment of psoriatic arthritis and to assess change in disease symptoms. Risankizumab is being studied for the treatment of jPsA and adalimumab is approved for the treatment of jPsA. Participants are placed in 1 of 2 groups, called treatment arms. Each group receives a different treatment. There is a 1 in 4 chance that participants will be assigned to receive adalimumab. Approximately 40 juvenile participants with jPsA will be enrolled at approximately 30 sites worldwide. Participants will receive risankizumab and adalimumab as subcutaneous (SC) injections based on body weight. At the start of Period 1, participants are randomized to receive risankizumab or adalimumab for 24 weeks. Participants who respond to the study treatment received in Period 1, will continue to receive the same treatment in Period 2 for another 100 weeks. Those with worsening jPsA symptoms in Period 2 will be withdrawn from the study. Participants who receive adalimumab are followed for safety for 70 days after the last study treatment. Participants who receive risankizumab are followed for 140 days after the last study treatment. There may …

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

Talk to the study team

ABBVIE CALL CENTER  ·  844-663-3742  ·  abbvieclinicaltrials@abbvie.com

Always discuss trial participation with your own doctor first.

Locations (33)

Arkansas Children's Hospital /ID# 258776Little Rock, Arkansas, United StatesRecruiting
Childrens National Medical Center /ID# 259284Washington D.C., District of Columbia, United StatesRecruiting
Joe Dimaggio Children's Hospital Hollywood /ID# 260634Hollywood, Florida, United StatesRecruiting
All X Ray Diagnostic Services Corp /ID# 278523Miami, Florida, United StatesRecruiting
Indiana University Health Riley Hospital for Children /ID# 259067Indianapolis, Indiana, United StatesRecruiting
M Health Fairview University of Minnesota Medical Center - West Bank /ID# 260111Minneapolis, Minnesota, United StatesRecruiting
Columbia University Medical Center /ID# 262587New York, New York, United StatesRecruiting
Boston Childrens Health Physicians /ID# 258061Valhalla, New York, United StatesRecruiting
University of North Carolina - Children's Hospital /ID# 259286Chapel Hill, North Carolina, United StatesRecruiting
MetroHealth Medical Center /ID# 262377Cleveland, Ohio, United StatesRecruiting
Child Neurology Consultants of Austin /ID# 260562Austin, Texas, United StatesRecruiting
Monash Health - Monash Medical Centre - Clayton /ID# 260255Clayton, Victoria, AustraliaRecruiting

+ 21 more locations — full list on the registry record.

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06100744