Patient Guide: A Study Comparing Risankizumab to Placebo in Participants With Active Psoriatic Arthritis Including Those Who Have a History of Inadequate Response or Intolerance to Biologic Therapy(Ies)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 138 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT03671148
Status: ACTIVE_NOT_RECRUITING
Condition: Psoriatic Arthritis (PsA)
Phase: PHASE3

Where You Can Participate

This study is available at 138 locations across the country.

Top locations include:
  • • Anniston, Alabama
  • • Fullerton, California
  • • Huntington Beach, California
  • • And 135 more locations

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A Study Comparing Risankizumab to Placebo in Participants With Active Psoriatic Arthritis Including Those Who Have a History of Inadequate Response or Intolerance to Biologic Therapy(Ies) - Join Clinical Trial NCTNCT03671148

How to Join This Clinical Trial - NCTNCT03671148

Learn how to participate in this PHASE3 trial studying an investigational therapy for Psoriatic Arthritis (PsA). Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Psoriatic Arthritis (PsA)
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT03671148 - 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 138 locations. Find a study site near you:

Clinical Research Site

Anniston, Alabama 36207 - United States

Status: Contact for availability

Clinical Research Site

Fullerton, California 92835 - United States

Status: Contact for availability

Clinical Research Site

Huntington Beach, California 92648-5994 - United States

Status: Contact for availability

Clinical Research Site

La Palma, California 90623-1728 - United States

Status: Contact for availability

Clinical Research Site

San Leandro, California 94578 - United States

Status: Contact for availability

Clinical Research Site

Upland, California 91786 - United States

Status: Contact for availability

Clinical Research Site

Denver, Colorado 80230 - United States

Status: Contact for availability

Clinical Research Site

Bridgeport, Connecticut 06606-1827 - United States

Status: Contact for availability

Clinical Research Site

New Haven, Connecticut 06510 - United States

Status: Contact for availability

Clinical Research Site

Aventura, Florida 33180 - United States

Status: Contact for availability

And 128 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 Psoriatic Arthritis (PsA):

  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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