Study of Targeted Therapies for the Treatment of Adult Participants With Active Psoriatic Arthritis
Purpose
Psoriatic arthritis (PsA) is a type of arthritis that happens when the body's immune system attacks healthy cells and tissues causing joint pain, stiffness, and swelling. Symptoms can get worse and go away for periods of time. This study will evaluate the efficacy and safety of targeted therapies through a series of substudies, for the treatment of active psoriatic arthritis and to assess the changes in disease symptoms. The therapies being assessed in this sub-study are risankizumab and lutikizumab. Participants will be randomized in a 1:1:1 ratio to one of the three treatment arms: lutikizumab monotherapy, risankizumab monotherapy or a combination therapy of lutikizumab and risankizumab. Around 120 participants will be enrolled in the study at approximately 40 sites worldwide. There may be higher treatment burden for participants in this trial compared to their standard of care (due to study procedures). Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, checking for side effects and completing questionnaires.
Condition
- Psoriatic Arthritis
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Participant is willing and able to comply with procedures required in the Master Protocol and substudies. - Participant has a documented clinical diagnosis of PsA with symptom onset at least 6 months prior to the Screening Visit and fulfillment of the Classification Criteria for Psoriatic Arthritis (CASPAR) at Screening Visit. - Participant has active disease defined as greater than or equal to 3 tender joints (based on 68 joint count) and greater than or equal to 3 swollen joints (based on 66 joint count) at both the Screening Visit and Baseline. - Participant has active plaque PsO and/or a documented history of plaque PsO. - Participant must demonstrate intolerance or inadequate response to 1 to 2 targeted therapies (biologic or targeted synthetic disease-modifying antirheumatic drugs) approved for the treatment of PsA
Exclusion Criteria
- Participants who have had major surgery performed within 12 weeks prior to randomization or plan to have a major surgery during conduct of the study (e.g., aneurysm removal, stomach ligation). - Participants with the following chronic or active infections: Are infected with human immunodeficiency virus (HIV), active hepatitis B virus (HBV) or hepatitis C virus(HCV) infection, active tuberculosis(TB) - Active skin disease other than psoriasis (PsO) which could interfere with the assessment of PsO. - History of fibromyalgia, any arthritis with onset prior to age 17 years, or current diagnosis of inflammatory joint disease other than psoriatic arthritis (PsA) (including but not limited to rheumatoid arthritis, gout, overlap connective tissue diseases, scleroderma, polymyositis, dermatomyositis, systemic lupus erythematosus).
Study Design
- Phase
- Phase 2
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Treatment
- Masking
- None (Open Label)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Sub-Study 1: Risankizumab Monotherapy |
Participants will receive Risankizumab |
|
|
Experimental Sub-Study 1: Lutikizumab Monotherapy |
Participants will initially receive Lutikizumab Dose A followed by Lutikizumab Dose B every other week. |
|
|
Experimental SubStudy 1: Lutikizumab and Risankizumab Combination Therapy |
Participants will be administered Lutikizumab and Risankizumab at the same time following the same dosing regimen as the monotherapy arms. |
|
Recruiting Locations
Huntington Beach 5358705, California 5332921 92648-5994
Site Coordinator
714-923-7112
Avon Park 4146440, Florida 4155751 33825
Site Coordinator
863-314-8555
Clearwater 4151316, Florida 4155751 33765
Orlando 4167147, Florida 4155751 32819
Tamarac 4174738, Florida 4155751 33321
Tampa 4174757, Florida 4155751 33606
Site Coordinator
(813) 870-1292
Skokie 4911600, Illinois 4896861 60076
Site Coordinator
847-599-2492
Willowbrook 4916709, Illinois 4896861 60527
Middleburg Heights 5162851, Ohio 5165418 44130
Duncansville 5187508, Pennsylvania 6254927 16635
Site Coordinator
814-296-6108
Memphis 4641239, Tennessee 4662168 38119
Austin 4671654, Texas 4736286 78745
Houston 4699066, Texas 4736286 77089-6142
Site Coordinator
281-481-8557
San Antonio 4726206, Texas 4736286 78251
Tomball 4737094, Texas 4736286 77375
More Details
- NCT ID
- NCT06865105
- Status
- Recruiting
- Sponsor
- AbbVie