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Juvenile Rheumatoid Arthritis |
Still's Disease |
Clinical Trial: ENBREL(R) (etanercept) as Treatment for Children with Systemic Onset Juvenile Rheumatoid Arthritis
This study is no longer recruiting patients.
|
Purpose
Rationale: etanercept inhibits the effects of tumor necrosis factor, which plays an important role in the progression of rheumatoid arthritis. A study of children with polyarticular course juvenile rheumatoid arthritis showed that Enbrel had efficacy and was generally well tolerated in children ages 4-17 who had moderately to severely active disease and who failed treatment with one or more disease modifying antiarthritic drugs. The children in the study may have had arthritis onset of pauciarticular, polyarticular, or systemic nature. Systemic onset juvenile rheumatoid arthritis (SOJRA) may result in approximately one-third of patients having significant long-term disability.
Purpose: the Phase 4 study is designed to further define the safety and efficacy of etanercept in those children with SOJRA.
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| Juvenile Rheumatoid Arthritis | Drug: Etanercept (ENBREL) | Phase IV |
MedlinePlus related topics: Juvenile Rheumatoid Arthritis
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Crossover Assignment, Safety/Efficacy Study
Official Title: A Phase 4 Safety and Efficacy Study of etanercept in Children with Systemic Onset Juvenile Rheumatoid Arthritis
Expected Total Enrollment: 75
Study start: June 2001; Study completion: June 2003
Eligibility
Ages Eligible for Study: 2 Years - 18 Years, Genders Eligible for Study: Both
Criteria
INCLUSION CRITERIA:
- 2 - 18 years of age
- SOJRA for at least 3 months, with stable systemic features
- If taking methotrexate, hydroxychloroquine, or NSAIDs, dose must be stable
- Must take prednisone at a stable dose
EXCLUSION CRITERIA:
- Need for other DMARDs or prestudy requirements for oral or parenteral pulse steroids or intra-articular steroids
- Pregnant or nursing female
- Clinically significant abnormal laboratory test results for blood cells, liver or kidney function, or serology
- Previous receipt of any TNF inhibitor
- Live virus vaccine within 12 weeks of study entry
- Participation in another study requiring informed consent within 12 weeks of entry
- Diabetes that requires insulin treatment
- Infection, chronic, recurrent, or currently active
- Any serious medical or psychiatric condition or history of alcohol or drug abuse
Location Information
Washington
Immunex Corporation, Seattle, Washington, 98101, United States
Wayne Tsuji, MD, Study Director, Immunex Corporation
More Information
Immunex Corporation
Publications
Lovell DJ, Giannini EH, Reiff A, Cawkwell GD, Silverman ED, Nocton JJ, Stein LD, Gedalia A, Ilowite NT, Wallace CA, Whitmore J, Finck BK. Etanercept in children with polyarticular juvenile rheumatoid arthritis. Pediatric Rheumatology Collaborative Study Group. N Engl J Med. 2000 Mar 16;342(11):763-9.
Moreland LW, Margolies G, Heck LW Jr, Saway A, Blosch C, Hanna R, Koopman WJ. Recombinant soluble tumor necrosis factor receptor (p80) fusion protein: toxicity and dose finding trial in refractory rheumatoid arthritis. J Rheumatol. 1996 Nov;23(11):1849-55.
Record last reviewed: July 2004
Last Updated: October 13, 2004
Record first received: June 17, 2002
ClinicalTrials.gov Identifier: NCT00039949
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005
Resources
- 2004 Drug Guide (Arthritis Foundation)
- American College of Rheumatology

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