Patient Guide: Study to Assess Change in Disease Activity and Adverse Events of Oral Upadacitinib Compared to Subcutaneous Adalimumab in Adult Participants With Moderate to Severe Rheumatoid Arthritis

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 218 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05814627
Status: ACTIVE_NOT_RECRUITING
Condition: Rheumatoid Arthritis
Phase: PHASE3

Where You Can Participate

This study is available at 218 locations across the country.

Top locations include:
  • • Flagstaff, Arizona
  • • Glendale, Arizona
  • • Peoria, Arizona
  • • And 215 more locations

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Study to Assess Change in Disease Activity and Adverse Events of Oral Upadacitinib Compared to Subcutaneous Adalimumab in Adult Participants With Moderate to Severe Rheumatoid Arthritis - Join Clinical Trial NCTNCT05814627

How to Join This Clinical Trial - NCTNCT05814627

Learn how to participate in this PHASE3 trial studying an investigational therapy for Rheumatoid Arthritis. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Rheumatoid Arthritis
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05814627 - 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 218 locations. Find a study site near you:

Clinical Research Site

Flagstaff, Arizona 86001-6299 - United States

Status: Contact for availability

Clinical Research Site

Glendale, Arizona 85306-9802 - United States

Status: Contact for availability

Clinical Research Site

Peoria, Arizona 85381 - United States

Status: Contact for availability

Clinical Research Site

Phoenix, Arizona 85032 - United States

Status: Contact for availability

Clinical Research Site

Phoenix, Arizona 85032 - United States

Status: Contact for availability

Clinical Research Site

Tucson, Arizona 85704 - United States

Status: Contact for availability

Clinical Research Site

Jonesboro, Arkansas 72401-6251 - 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 Mesa, California 91942 - United States

Status: Contact for availability

And 208 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 Rheumatoid 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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