Patient Guide: An Observational Study to Assess Change in Disease Activity and Treatment Patterns of Upadacitinib When Given Alone or Co-Administered With Methotrexate in Adult Participants With Active Psoriatic Arthritis

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 88 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05616871
Status: ACTIVE_NOT_RECRUITING
Condition: Psoriatic Arthritis
Phase: Research Study

Where You Can Participate

This study is available at 88 locations across the country.

Top locations include:
  • • Nice CEDEX 1, Alpes-Maritimes
  • • Troyes, Aube
  • • Besancon, Doubs
  • • And 85 more locations

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An Observational Study to Assess Change in Disease Activity and Treatment Patterns of Upadacitinib When Given Alone or Co-Administered With Methotrexate in Adult Participants With Active Psoriatic Arthritis - Join Clinical Trial NCTNCT05616871

How to Join This Clinical Trial - NCTNCT05616871

Learn how to participate in this clinical trial studying an investigational therapy for Psoriatic Arthritis. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with 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
Psoriatic Arthritis
Treatment Being Tested
Investigational treatment
Study Phase
Clinical trial phase - Research study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05616871 - 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 88 locations. Find a study site near you:

Clinical Research Site

Nice CEDEX 1, Alpes-Maritimes 06001 - France

Status: Contact for availability

Clinical Research Site

Troyes, Aube 10000 - France

Status: Contact for availability

Clinical Research Site

Besancon, Doubs 25030 - France

Status: Contact for availability

Clinical Research Site

Limoges CEDEX 1, Franche-Comte 87042 - France

Status: Contact for availability

Clinical Research Site

TOULOUSE Cedex 9, Haute-Garonne 31059 - France

Status: Contact for availability

Clinical Research Site

Montpellier Cedex 5, Herault 34295 - France

Status: Contact for availability

Clinical Research Site

La Tronche, Isere 38700 - France

Status: Contact for availability

Clinical Research Site

Bordeaux, Nouvelle-Aquitaine 33076 - France

Status: Contact for availability

Clinical Research Site

Beauvais CEDEX, Oise 60021 - France

Status: Contact for availability

Clinical Research Site

Creteil, Paris 94010 - France

Status: Contact for availability

And 78 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this clinical trial for 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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