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)
Purpose
The main purpose of this study is to assess the effectiveness of adding tirzepatide to ixekizumab therapy in standard clinical practice in participants with moderate-to-severe PsA and obesity or overweight with at least 1 weight-related comorbidity. The study will last up to 12 months.
Conditions
- Psoriatic Arthritis
- Overweight or Obesity
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion 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 exposure to tirzepatide or other glucagon-like peptide-1 (GLP-1) receptor agonist (for example, dulaglutide, liraglutide, or semaglutide). - Are currently enrolled in any other clinical study. - Have a known hypersensitivity to any component of tirzepatide. - Have a personal or family history of medullary thyroid cancer. - Have multiple endocrine neoplasia type 2. - Have type 1 diabetes mellitus. - Have a history of chronic or acute pancreatitis at any time before screening. - Have a history of proliferative diabetic retinopathy, diabetic maculopathy, or nonproliferative diabetic retinopathy that requires acute treatment. - Have a history of ketoacidosis or hyperosmolar state/coma. - Have a history of severe hypoglycemia unawareness within the 6 months before screening. - Have a history of severe gastrointestinal complications, including gastroparesis, gastroesophageal reflux disease, dyspepsia, chronic nausea/vomiting.
Study Design
- Phase
- Phase 4
- Study Type
- Interventional
- Allocation
- N/A
- Intervention Model
- Single Group Assignment
- Primary Purpose
- Treatment
- Masking
- None (Open Label)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Tirzepatide |
Participants will continue on ixekizumab and take tirzepatide administered subcutaneously (SC) as per label. |
|
Recruiting Locations
Avondale 5552301, Arizona 5551752 85392
602-386-4971
Chandler 5289282, Arizona 5551752 85225
480-443-8400
Flagstaff 5294810, Arizona 5551752 86001
928-666-3772
Gilbert 5295903, Arizona 5551752 85297
480-443-8400
Glendale 5295985, Arizona 5551752 85306
602-386-4969
Mesa 5304391, Arizona 5551752 85210
480-626-6637
Phoenix 5308655, Arizona 5551752 85032
480-626-6637
Sun City 5316201, Arizona 5551752 85351
602-386-4970
Tucson 5318313, Arizona 5551752 85704
520-867-6906
Tucson 5318313, Arizona 5551752 85748
520-849-8753
Apple Valley 5324363, California 5332921 92307
909-581-8477
Covina 5340175, California 5332921 91722
626-869-5730
Huntington Beach 5358705, California 5332921 92648
714-378-2440
La Mesa 5363990, California 5332921 91942
619-229-1995 x208
Riverside 5387877, California 5332921 92508
951-672-1866
San Diego 5391811, California 5332921 92128
Santa Monica 5393212, California 5332921 90404
Temecula 5401395, California 5332921 92592
951-652-5000
Tujunga 5403767, California 5332921 91042
818-265-2250
Whittier 5409059, California 5332921 90602
562-758-6600
Kissimmee 4160983, Florida 4155751 34741
Margate 4163407, Florida 4155751 33063
Miami Beach 4164143, Florida 4155751 33140
Palm Beach Gardens 4167519, Florida 4155751 33410
561-559-1110
Tampa 4174757, Florida 4155751 33614
Marietta 4207783, Georgia 4197000 30060
770-372-3962
Waycross 4229763, Georgia 4197000 31501
912-548-0710
Chicago 4887398, Illinois 4896861 60640
773-275-3500
Schaumburg 4910713, Illinois 4896861 60195
847-599-2492
Skokie 4911600, Illinois 4896861 60076
Willowbrook 4916709, Illinois 4896861 60527
434-962-8466
New Albany 4262045, Indiana 4921868 47150
502-495-3665
Lake Charles 4330236, Louisiana 4331987 70605
337-312-8018
Cumberland 4352681, Maryland 4361885 21502
301-724-4337
Hagerstown 4357141, Maryland 4361885 21740
301-791-6680
Saint Clair Shores 5010978, Michigan 5001836 48081
Kalispell 5660340, Montana 5667009 59901
406-752-2010
Rochester 5134086, New York 5128638 14642
Salisbury 4489985, North Carolina 4482348 28144
800-785-3150
Middleburg Heights 5162851, Ohio 5165418 44130
440-826-0742
Tulsa 4553433, Oklahoma 4544379 74137
Jackson 4632595, Tennessee 4662168 38305
731-633-0145
Murfreesboro 4644312, Tennessee 4662168 37128
480-626-6650
Colleyville 4682478, Texas 4736286 76034
972-299-8399
Fort Worth 4691930, Texas 4736286 76109
817-789-6770
Houston 4699066, Texas 4736286 77089
281-481-8557
Houston 4699066, Texas 4736286 77089
281-944-3610
Irving 4700168, Texas 4736286 75039
Katy 4702732, Texas 4736286 77494
281-944-3610
The Woodlands 4736476, Texas 4736286 77382
936-681-4882
Tomball 4737094, Texas 4736286 77375
281-517-0550
Seattle 5809844, Washington 5815135 98104
Spokane Valley 5811729, Washington 5815135 99216
Guaynabo 4565119, Puerto Rico 00968
939-599-0382
San Juan 4568127, Puerto Rico 00918
More Details
- NCT ID
- NCT06864026
- Status
- Recruiting
- Sponsor
- Eli Lilly and Company
Study Contact
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or1-317-615-4559
LillyTrials@Lilly.com