Meloxicam |
Mobic |
Clinical Trial: Meloxicam suspension in Juvenile Rheumatoid Arthritis (JRA)
This study has been completed.
|
Purpose
The purpose of this 6 month study is to determine how safe and effective meloxicam oral suspension (liquid taken by mouth) is in children with JRA.
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| Juvenile Rheumatoid Arthritis | Drug: Meloxicam | Phase III |
MedlinePlus related topics: Juvenile Rheumatoid Arthritis
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title: A 12 wk double-blind randomized trial, with a 12 wk open-label extension, to investigate efficacy and safety of meloxicam oral suspension administered once daily and naproxen oral suspension administered twice daily in children with JRA.
Expected Total Enrollment: 180
Study start: December 2000; Study completion: June 2003
The primary aim of this trial is to compare the efficacy and safety of several doses of meloxicam oral suspension (0.125 mg/kg and 0.25 mg/kg with a 0.125 mg/kg dose escalation at 4 weeks) administered once daily with naproxen oral suspension (10 mg/kg with a dose escalation to15 mg/kg at 4 weeks administered in divided doses twice daily) over a period of 12 weeks in the treatment of patients with JRA. The 12-week double-blind portion of the trial is followed by an open-label extension of meloxicam oral suspension at 0.375 mg/kg/day to obtain additional safety information. A subgroup of patients will participate in a pharmacokinetic study at the conclusion of the open label extension phase.
Eligibility
Ages Eligible for Study: 2 Years - 17 Years, Genders Eligible for Study: Both
Criteria
Inclusion Criteria:
- Males or females 2-17 years old.
- Diagnosis of JRA for at least 6 weeks, onset of disease less than 16 years old.
- Current course of disease pauciarthritic, extended pauciarthritic, or polyarthritic.
- Active arthritis of at least 2 joints.
- Patient requires therapy with an NSAID.
- At screening, patient has at least 2 abnormal variables among the following: CHAQ, ESR, Investigator’s Assessment of Overall Disease Activity, or Parent’s Assessment of Overall Well-Being.
Exclusion Criteria:
- Systemic course of JRA
- Weight less than 9kg
- History of bleeding disorders, gastrointestinal bleeding, peptic ulcer, cerebrovascular bleeding, rheumatic conditions other than JRA, or any disease that could interfere with the trial or the child’s safety.
Location Information
Arkansas
Arkansas Children's Hospital, Little Rock, Arkansas, 72202, United States
California
Valley Children's Hospital, Rheumatology Dept., Madera, California, 93738, United States
Children's Hospital Research Clinic, San Diego, California, 92123, United States
Colorado
Children's Hospital, Denver, Colorado, 80218, United States
Florida
Miami Children's Hospital, Miami, Florida, 33155, United States
Arthritis Association Clinical Research of So. Florida, Delray Beach, Florida, 33484, United States
All Children's Hospital, St. Petersburg, Florida, 33701, United States
Kentucky
University of Louisville, Dept. of Pediatrics, Louisville, Kentucky, 40202, United States
Louisiana
Children's Hospital, Dept. of Rheumatology, New Orleans, Louisiana, 70118, United States
Massachusetts
Children's Hospital Medical Center, Dept. of Rheumatology, Boston, Massachusetts, 02115, United States
Minnesota
E15 Mayo Clinic, Rochester, Minnesota, 55905, United States
Missouri
Washington University School of Medicine, St. Louis, Missouri, 63110, United States
Nebraska
Creighton University, Dept. of Pediatrics, Omaha, Nebraska, 68178, United States
New Jersey
Arthritis and Rheumatic Disease Center, Livingston, New Jersey, 07039, United States
New York
Columbia Presbyterian Medical Center, New York, New York, 10032, United States
The Children's Hospital of Buffalo, Div. of Allergy, Immunology and Rheumatology, Buffalo, New York, 14222, United States
Oklahoma
Oklahoma Medical Research Foundation, Div. of Rheumatology, Oklahoma City, Oklahoma, 73104, United States
HealthCare Research Consultants, Tulsa, Oklahoma, 74135, United States
Pennsylvania
Arthritis and Osteoporosis Center, Duncansville, Pennsylvania, 16635, United States
Rhode Island
Div. of Ambulatory Pediatrics, Hasbro Children's Hospital, Providence, Rhode Island, 02903, United States
Texas
Texas Scottish Rite Hospital, Dept. of Pediatric Rheumatology, Dallas, Texas, 75219, United States
Utah
University of Utah School of Medicine, Dept. of Pediatrics, Salt Lake City, Utah, 84132, United States
Washington
Children's Hospital, Pediatric Rheumatology, Seattle, Washington, 98105, United States
Wisconsin
Medical College of Wisconsin, Dept. of Pediatrics, Milwaukee, Wisconsin, 53226, United States
Argentina
Hospital de Ninos, Buenos Aires, 01430, Argentina
Brazil
Epm Universidade Federal de Sao Paulo, Sao Paulo, 04025, Brazil
Mexico
Hospital General de Mexico, Mexico City, 06726, Mexico
More Information
Record last reviewed: November 2003
Last Updated: October 13, 2004
Record first received: May 2, 2002
ClinicalTrials.gov Identifier: NCT00034853
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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