Last reviewed · How we verify
A Randomized, Multi-center, Blinded, Placebo-controlled Study With an Open-label Run-in Period to Evaluate the Efficacy, Safety, and Pharmacokinetics of Daily, Single, Subcutaneous Injections of r-metHuIL-1ra (Anakinra) in Polyarticular-Course Juvenile Rheumatoid Arthritis
The purpose of this study is to determine the safety of anakinra in patients with Polyarticular-Course Juvenile Rheumatoid Arthritis, a form of rheumatoid arthritis affecting children.
Details
| Lead sponsor | Amgen |
|---|---|
| Phase | Phase 2 |
| Status | COMPLETED |
| Enrolment | 86 |
| Start date | 2000-07 |
| Completion | 2003-11 |
Conditions
- Juvenile Chronic Arthritis
Interventions
- Anakinra
- Placebo
Primary outcomes
- The primary outcome of the study was to evaluate the safety of anakinra — 28 weeks