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ENBREL(R) (etanercept) as Treatment for Children with Systemic Onset Juvenile Rheumatoid Arthritis - Article


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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.

Sponsored by: Immunex Corporation
Information provided by: Immunex Corporation

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

Further Study Details: 

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

Study chairs or principal investigators

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.

Study ID Numbers:  016.0031
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

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December 1, 2008



Page Updated: October 3, 2005
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