Patient Guide: 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

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 28 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06100744
Status: 🟢 Enrolling Now
Condition: Juvenile Psoriatic Arthritis
Phase: PHASE3

Where You Can Participate

This study is available at 28 locations across the country.

Top locations include:
  • • Little Rock, Arkansas
  • • Washington, District of Columbia
  • • Hollywood, Florida
  • • And 25 more locations

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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 - Join Clinical Trial NCTNCT06100744

How to Join This Clinical Trial - NCTNCT06100744

Learn how to participate in this PHASE3 trial studying an investigational therapy for Juvenile Psoriatic Arthritis. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Juvenile Psoriatic Arthritis. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Juvenile Psoriatic Arthritis
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06100744 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 28 locations. Find a study site near you:

Clinical Research Site

Little Rock, Arkansas 72202 - United States

Status: RECRUITING

Clinical Research Site

Washington, District of Columbia 20010-2916 - United States

Status: RECRUITING

Clinical Research Site

Hollywood, Florida 33021 - United States

Status: RECRUITING

Clinical Research Site

Indianapolis, Indiana 46202 - United States

Status: RECRUITING

Clinical Research Site

Minneapolis, Minnesota 55454 - United States

Status: RECRUITING

Clinical Research Site

Valhalla, New York 10595 - United States

Status: RECRUITING

Clinical Research Site

Chapel Hill, North Carolina 27514 - United States

Status: RECRUITING

Clinical Research Site

Cleveland, Ohio 44109 - United States

Status: RECRUITING

Clinical Research Site

Austin, Texas 78757-7571 - United States

Status: RECRUITING

Clinical Research Site

Clayton, Victoria 3168 - Australia

Status: RECRUITING

And 18 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Juvenile Psoriatic Arthritis:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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