Phase III Study of Efficacy and Safety of Secukinumab Versus Placebo, in Combination With Glucocorticoid Taper Regimen, in Patients With Giant Cell Arteritis (GCA)
Part of paid clinical trials in Los Angeles, California.
- Sponsor
- Novartis Pharmaceuticals
- Study ID
- NCT04930094
- Phase
- PHASE3
- Status
- Completed
Conditions
- Giant Cell Arteritis (GCA)
Eligibility Criteria
- Sex
- ALL
- Age
- 50 Years - 100 Years
- Healthy Volunteers
- Not accepted
Interventions
- Secukinumab 300 mg — BIOLOGICALSecukinumab 300 mg
- Placebo — OTHERPlacebo
- Secukinumab 150 mg — BIOLOGICALSecukinumab
Study Details
This is a phase III study of efficacy and safety of secukinumab versus placebo, in combination with glucocorticoid taper regimen, in patients with giant cell arteritis (GCA)
Key Dates
- Start date
- Oct 6, 2021
- Status verified
- Mar 2026
- Primary completion
- Apr 11, 2025
- Completion
- Feb 18, 2026
Study Design
- Enrollment
- 354 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Secukinumab 300 mgSecukinumab 300 mg s.c. at BSL, Weeks 1, 2, 3, followed by administration every four weeks starting at Week 4. Secukinumab will be given in combination with a specified 26-week prednisone taper regimen. After the 26-week prednisone taper, participants will continue to receive placebo to prednisone until Week 52.
- Placebo Comparator: PlaceboPlacebo to secukinumab s.c. at BSL, Weeks 1, 2, 3, followed by administration every four weeks starting at Week 4. Placebo will be given in combination with a specified 52-week prednisone taper regimen.
- Experimental: Secukinumab 150 mgSecukinumab 150 mg s.c. at BSL, Weeks 1, 2, 3, followed by administration every four weeks starting at Week 4. Secukinumab will be given in combination with a specified 26-week prednisone taper regimen. After the 26-week prednisone taper, participants will continue to receive placebo to prednisone until Week 52.
Primary Outcome Measure
Proportion of participants with sustained remission [ Time Frame: 52 weeks ]
Locations (10)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Cedars Sinai Medical Center | Los Angeles | California | 90048 | - |
| IRIS Research and Development | Plantation | Florida | 33324 | - |
| Sarasota Arthritis Res Ctr | Sarasota | Florida | 34239 | - |
| Novartis Investigative Site | Iowa City | Iowa | 52242 | - |
| University Of Iowa | Iowa City | Iowa | 52242 | - |
| Osteoporosis and Clinical Trial Ctr | Hagerstown | Maryland | 21740 | - |
| Massachusetts General Hospital | Boston | Massachusetts | 02114 | - |
| West Tennessee Research Institute | Jackson | Tennessee | 38305 | - |
| Precision Comp Clin Research | Grapevine | Texas | 76051 | - |
| Advanced Rheumatology of Houston | Spring | Texas | 77382 | - |
Related coverage on Hipa.ai
- Secukinumab Phase 3 GCA Trial Completes Primary Data CollectionSecukinumab · Apr 11, 2025 · ClinicalTrials.gov
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