Status:
COMPLETED
Infliximab Plus Intravenous Immunoglobulin for the Primary Treatment of Kawasaki Disease
Lead Sponsor:
University of California, San Diego
Collaborating Sponsors:
Nationwide Children's Hospital
Conditions:
Kawasaki Disease
Eligibility:
All Genders
4-17 years
Phase:
PHASE3
Brief Summary
The purpose of this study is to determine whether the addition of infliximab to standard primary therapy of intravenous immunoglobulin (IVIG) and high dose aspirin will reduce resistance to therapy in...
Detailed Description
KD, an orphan disease of low prevalence in U.S. children, causes significant long term cardiac sequelae in a subset of patients. KD patients that are resistant to therapy are more likely to develop co...
Eligibility Criteria
Inclusion
- All eligible subjects, or legal representative, must provide written informed consent/assent, prior to initiation of any study procedure.
- Eligible subjects will be infants and children, 4 weeks to 17 years old, who have had fever for 3 to 15 days (illness day 1 = first day of fever ≥ 38.3° C)
- Patients who meet one of the following sets of criteria will be eligible for enrollment (adapted from AHA guidelines: Newburger et al. 2004):
- Case definition for complete KD: Fever (≥ 38.3°C) for ≥ 3 days and 4/5 standard clinical criteria (Table 1)
- Case definition for incomplete KD: Fever ≥ 5 days and 2-3 clinical criteria plus either C-reactive protein (CRP) ≥ 3.0 mg/dL or ESR ≥40 mm/hr AND ≥ 3 supplemental laboratory criteria: albumin ≤ 3.0 g/dl, anemia for age, ALT ≥ 45, platelet count ≥ 450,000/mm3, white blood cell count ≥ 15,000/mm3, or urinalysis with ≥10 white blood cells/hpf.
- Case definition for incomplete KD with echocardiogram data: Fever ≥ 5 days and \<4/5 clinical criteria plus abnormal echocardiogram with z score of LAD or RCA ≥ 2.5
- Females of childbearing potential and males must be using adequate contraception (abstinence, oral contraceptives, intrauterine device, barrier method with spermicide, or surgical sterilization) throughout the trial.
- All eligible subjects must have a chest radiograph within one week prior to first infusion of study drug with no evidence of tuberculosis or other infection.
Exclusion
- Have been receiving corticosteroids (i.e. via any route) at doses \> 1 mg/kg prednisone equivalent daily.
- History of tuberculosis (TB) or TB exposure.
- Have received a BCG vaccination within the past 6 months.
- History of histoplasmosis or coccidioidomycosis
- Have received anakinra (Kineret®), etanercept (Enbrel®), or adalimumab (Humira®) within 1 month prior to first study drug administration.
- Have any chronic disease, except asthma, atopic dermatitis or controlled seizure disorder.
- Have documented history of current active Hepatitis B or a history of Hepatitis C infection.
- Have a documented history of human immunodeficiency virus (HIV) infection.
- Have received a transplanted organ (with the exception of a corneal transplant performed \> 3 months prior to the first study drug administration).
- Have a known malignancy or history of malignancy within the 5-year period prior to first study drug administration (with the exception of basal cell or squamous cell carcinoma of the skin that has been completely excised without evidence of recurrence).
- Have a history of prior lymphoproliferative disease including lymphoma.
- Have multiple sclerosis or other central demyelinating disorder.
- Have received any previous treatment with infliximab or other monoclonal antibodies
- Have used any investigational drug within 1 month prior to first study drug administration or within 5 half-lives of the investigational agent, whichever is longer.
- Are participating in another investigative trial, involving investigational agents, during participation in this trial.
- Have a history of substance abuse (drug or alcohol) within the previous 3 years.
- Are pregnant, nursing, or planning pregnancy (both men and women) during the trial or within the 6-month period thereafter.
- Have a known allergy to murine proteins or other chimeric proteins.
- Patients with ischemic congestive heart failure, defined by ECG changes, elevated Troponin 1 and CPK-MB consistent with myocardial ischemia.
- Have an abnormal chest radiograph
- Afebrile for ≥ 48 hours
Key Trial Info
Start Date :
March 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2012
Estimated Enrollment :
196 Patients enrolled
Trial Details
Trial ID
NCT00760435
Start Date
March 1 2009
End Date
October 1 2012
Last Update
November 24 2014
Active Locations (2)
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1
University of California, San Diego
La Jolla, California, United States, 92093
2
Nationwide Children's Hospital
Columbus, Ohio, United States