A Study of RoActemra/Actemra (Tocilizumab) Given Subcutaneously in Combination With Traditional DMARDs in Patients With Moderate to Severe Active Rheumatoid Arthritis
Part of paid clinical trials in Peoria, Arizona.
- Sponsor
- Hoffmann-La Roche
- Study ID
- NCT01232569
- Phase
- PHASE3
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Tocilizumab 162 mg — DRUGTocilizumab will be supplied in a ready-to-use, single-use, pre-filled syringe. Patients and/or caregivers will be trained to administer the injection.
- Placebo — DRUGPlacebo will be supplied in a ready-to-use, single-use, pre-filled syringe. Patients and/or caregivers will be trained to administer the injection.
Study Details
This randomized, parallel-group, placebo-controlled, multicenter study will evaluate the reduction in disease activity and the safety of tocilizumab (RoActemra/Actemra) in combination with traditional disease-modifying anti-rheumatic drugs (DMARDs) in patients with active, moderate to severe rheumatoid arthritis. In the double-blind part of the study, patients will be randomized to receive either 162 mg tocilizumab or placebo subcutaneously every 2 weeks for 24 weeks using a pre-filled syringe. In the open-label part of the study, patients will be randomized to receive 162 mg tocilizumab subcutaneously every 2 weeks from Week 24 to Week 96 using a pre-filled syringe or an auto-injector.
Key Dates
- Start date
- Mar 31, 2011
- Status verified
- Jul 2015
- Primary completion
- May 31, 2012
- Completion
- Nov 30, 2013
Study Design
- Enrollment
- 656 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Tocilizumab 162 mg scPatients will receive tocilizumab 162 mg subcutaneously (sc) every 2 weeks for 24 weeks.
- Placebo Comparator: Placebo scPatients will receive placebo subcutaneously (sc) every 2 weeks for 24 weeks.
Primary Outcome Measure
Percentage of Patients With an American College of Rheumatology 20 (ACR20) Response at Week 24 [ Time Frame: Baseline to Week 24 ]
Locations (44)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| - | Peoria | Arizona | 85381 | - |
| - | Scottsdale | Arizona | 85258 | - |
| - | Tucson | Arizona | 85723 | - |
| - | Tucson | Arizona | 85724 | - |
| - | Fullerton | California | 92835 | - |
| - | San Diego | California | 92108 | - |
| - | San Leandro | California | 94578 | - |
| - | West Hills | California | 91307 | - |
| - | Trumbull | Connecticut | 06611 | - |
| - | Boca Raton | Florida | 33486 | - |
| - | Jupiter | Florida | 33458 | - |
| - | Ormond Beach | Florida | 32174 | - |
| - | Sarasota | Florida | 34292 | - |
| - | Gainesville | Georgia | 30501 | - |
| - | Idaho Falls | Idaho | 83404 | - |
| - | Meridan | Idaho | 83642 | - |
| - | Springfield | Illinois | 62704 | - |
| - | Vernon Hills | Illinois | 60061 | - |
| - | Crofton | Maryland | 21114 | - |
| - | Hagerstown | Maryland | 21740 | - |
| - | Wheaton | Maryland | 20902 | - |
| - | Flowood | Mississippi | 39232 | - |
| - | Jackson | Mississippi | 39202 | - |
| - | St Louis | Missouri | 63128 | - |
| - | St Louis | Missouri | 63141 | - |
| - | Lincoln | Nebraska | 68516 | - |
| - | Brooklyn | New York | 11201 | - |
| - | Belmont | North Carolina | 28012 | - |
| - | Charlotte | North Carolina | 28204 | - |
| - | Charlotte | North Carolina | 28207 | - |
| - | Charlotte | North Carolina | 28211 | - |
| - | Oklahoma City | Oklahoma | 73104 | - |
| - | Allentown | Pennsylvania | 18103 | - |
| - | Bethlehem | Pennsylvania | 18015 | - |
| - | Duncansville | Pennsylvania | 16635 | - |
| - | Wexford | Pennsylvania | 15090 | - |
| - | Wyomissing | Pennsylvania | 19610 | - |
| - | Memphis | Tennessee | 38104 | - |
| - | Dallas | Texas | 75246 | - |
| - | Fort Worth | Texas | 76107 | - |
| - | Houston | Texas | 77034 | - |
| - | Houston | Texas | 77459 | - |
| - | San Antonio | Texas | 78232 | - |
| - | Tacoma | Washington | 98405 | - |
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