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A Study to Investigate Effectiveness of Tirzepatide Following Initiation of Ixekizumab in

The main purpose of this study is to assess the effectiveness of adding tirzepatide to ixekizumab therapy in standard clinical practice in participants with active PsA and obesity or overweight with at least 1 weight-related comorbidity. The study will last up to 12 months.

Condition(s)Psoriatic Arthritis, Overweight or Obesity
StatusRecruiting
PhasePhase 4
Study typeInterventional
SummaryThe main purpose of this study is to assess the effectiveness of adding tirzepatide to ixekizumab therapy in standard clinical practice in participants with active PsA and obesity or overweight with at least 1 weight-related comorbidity. The study will last up to 12 months.
Who can participateInclusion Criteria: * Have a diagnosis of active psoriatic arthritis (PsA) as defined by a rheumatologist or other healthcare professional (HCP) experienced in treating PsA. * Body Mass Index (BMI) of 30 kilograms per meter squared (kg/m²) or greater (obesity) or 27 kg/m2 to \<30 kg/m² (overweight) in the presence of at least 1 weight-related comorbid condition (hypertension, dyslipidemia, type 2 diabetes, obstructive sleep apnea, or cardiovascular disease). * Who have been treated with ixekizumab for approximately 3 months (±1 month) prior to decision to add tirzepatide. * Must be able to initiate tirzepatide (Day 0) within 30 days of treatment decision (baseline or screening). Exclusion Criteria: * Have currently received ixekizumab for more than 4 months or less than 2 months. * Had any
Ages18 Years
SexAll
Lead sponsorEli Lilly and Company
LocationsAvondale, Arizona, United States; Chandler, Arizona, United States; Flagstaff, Arizona, United States; Gilbert, Arizona, United States; Glendale, Arizona, United States; Mesa, Arizona, United States (+49 more sites)
Start date2025-03-06
NCT IDNCT06864026
Official listinghttps://clinicaltrials.gov/study/NCT06864026

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