Patient Guide: A Study to Investigate the Effectiveness of Tirzepatide (LY3298176) Following Initiation of Ixekizumab (LY2439821) in Participants With Moderate-to-Severe Plaque PsO and Obesity or Overweight in Clinical Practice (TOGETHER AMPLIFY-PsO)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 45 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06857942
Status: 🟢 Enrolling Now
Condition: Psoriasis, Overweight or Obesity
Phase: PHASE4

Where You Can Participate

This study is available at 45 locations across the country.

Top locations include:
  • • Phoenix, Arizona
  • • Fountain Valley, California
  • • Fremont, California
  • • And 42 more locations

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A Study to Investigate the Effectiveness of Tirzepatide (LY3298176) Following Initiation of Ixekizumab (LY2439821) in Participants With Moderate-to-Severe Plaque PsO and Obesity or Overweight in Clinical Practice (TOGETHER AMPLIFY-PsO) - Join Clinical Trial NCTNCT06857942

How to Join This Clinical Trial - NCTNCT06857942

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

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Psoriasis, Overweight or Obesity
Treatment Being Tested
Investigational treatment
Study Phase
PHASE4 - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06857942 - 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 45 locations. Find a study site near you:

Clinical Research Site

Phoenix, Arizona 85006 - United States

Status: RECRUITING

Clinical Research Site

Fountain Valley, California 92708 - United States

Status: RECRUITING

Clinical Research Site

Fremont, California 94538 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Los Angeles, California 90017 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Northridge, California 91325 - United States

Status: RECRUITING

Clinical Research Site

Fort Myers, Florida 33912 - United States

Status: RECRUITING

Clinical Research Site

Hialeah, Florida 33016 - United States

Status: RECRUITING

Clinical Research Site

Hollywood, Florida 33021 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Hollywood, Florida 33024 - United States

Status: RECRUITING

Clinical Research Site

Tampa, Florida 33609 - United States

Status: RECRUITING

And 35 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 Psoriasis, Overweight or Obesity:

  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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