Patient Guide: A Study to Investigate Effectiveness of Tirzepatide Following Initiation of Ixekizumab in Participants With Active Psoriatic Arthritis and Overweight or Obesity in Clinical Practice (TOGETHER AMPLIFY-PsA)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 57 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06864026
Status: 🟢 Enrolling Now
Condition: Arthritis, Arthritis, Psoriatic, Obesity, Overweight
Phase: PHASE4

Where You Can Participate

This study is available at 57 locations across the country.

Top locations include:
  • • Avondale, Arizona
  • • Chandler, Arizona
  • • Flagstaff, Arizona
  • • And 54 more locations

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A Study to Investigate Effectiveness of Tirzepatide Following Initiation of Ixekizumab in Participants With Active Psoriatic Arthritis and Overweight or Obesity in Clinical Practice (TOGETHER AMPLIFY-PsA) - Join Clinical Trial NCTNCT06864026

How to Join This Clinical Trial - NCTNCT06864026

Learn how to participate in this PHASE4 trial studying an investigational therapy for Arthritis, Arthritis, Psoriatic, Obesity, Overweight. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Arthritis, Arthritis, Psoriatic, Obesity, Overweight
Treatment Being Tested
Investigational treatment
Study Phase
PHASE4 - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06864026 - 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 57 locations. Find a study site near you:

Clinical Research Site

Avondale, Arizona 85392 - United States

Status: RECRUITING

Clinical Research Site

Chandler, Arizona 85225 - United States

Status: RECRUITING

Clinical Research Site

Flagstaff, Arizona 86001 - United States

Status: RECRUITING

Clinical Research Site

Gilbert, Arizona 85297 - United States

Status: RECRUITING

Clinical Research Site

Glendale, Arizona 85306 - United States

Status: RECRUITING

Clinical Research Site

Mesa, Arizona 85210 - United States

Status: RECRUITING

Clinical Research Site

Phoenix, Arizona 85032 - United States

Status: RECRUITING

Clinical Research Site

Sun City, Arizona 85351 - United States

Status: RECRUITING

Clinical Research Site

Tucson, Arizona 85704 - United States

Status: RECRUITING

Clinical Research Site

Tucson, Arizona 85748 - United States

Status: RECRUITING

And 47 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE4 clinical trial for Arthritis, Arthritis, Psoriatic, Obesity, Overweight:

  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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