Combination of Biologic and Anti-obesity Therapies in Psoriatic Arthritis
- Sponsor
- NHS Greater Glasgow and Clyde
- Study ID
- NCT07443956
- Status
- Recruiting
Conditions
- Obesity & Overweight
- Psoriatic Arthritis (PsA)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Ixekizumab — DRUGanti-IL17A monoclonal antibody
- Tirzepatide — DRUGGLP-1 and GIP agonist
Study Details
This is a trial to find out how weight loss (achieved by the use of tirzepatide) or ixekizumab treatment affects the characteristics of skin, joint and fat tissues in patients with Psoriatic Arthritis, Psoriasis and obesity/overweight BMI \>=27. Participants will be allocated either Tirzepatide, Ixekizumab or both. Samples of joint tissue, fat and skin will be taken at the start of the study and week 12. Blood and urine samples will also be taken. The primary objective will be to assess the changes seen in the joint, fat and skin tissue samples 12 weeks after starting the medications (additional analysis will be done on the optional 36 week samples). Secondary objectives will be * To assess the changes seen in blood 4, 12, 36 and 52 weeks after starting the medication. * To compare the changes seen in tissue and blood between Ixekizumab and Tirzepatide/Weight loss. * To see how the changes seen in the tissue relate to weight loss.
Key Dates
- Start date
- Mar 9, 2026
- Status verified
- Apr 2026
- Primary completion
- Feb 29, 2028
- Completion
- May 31, 2030
Study Design
- Enrollment
- 45 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- BASIC_SCIENCE
Arms
- Active Comparator: Tirzepatide group
- Active Comparator: Ixekizumab group
- Active Comparator: Combined tirzepatide and ixekizumab
Primary Outcome Measure
Correlation of molecular changes in biopsies (skin, synovial and adipose) with weight loss [ Time Frame: 12 weeks ]
Central Contacts
- Stefan Siebert, MBBCh, FRCP, PhD+44 141 330 3375
- Project Manager+44 141 330 8408
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