Infliximab (Remicade) for Patients With Acute Kawasaki Disease

NCT ID: NCT00271570

Last Updated: 2010-06-14

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2004-04-30
• Study Completion Date: 2006-10-31

Brief Summary

This study evaluates the safety of infliximab in infants and children with acute Kawasaki Disease.

Detailed Description

This study is an exploratory, pilot study to examine tolerance and pharmacokinetics of infliximab in infants and children with acute Kawasaki Disease.

Conditions

Kawasaki Disease

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Second Dose of IVIG (2g/kg)

Subjects who did not respond to the first dose of IVIG received a 2nd dose of IVIG in this arm (2g/kg)

Group Type: ACTIVE_COMPARATOR

Intravenous immunoglobulin (IVIG)

Intervention Type: BIOLOGICAL

2nd dose of IVIG (2g/kg)

Infliximab (5mg/kg)

Remicade (5mg/kg) single dose

Group Type: EXPERIMENTAL

Infliximab (Remicade)

Intervention Type: DRUG

Remicade was 5 mg/kg IV (single dose)

Interventions

Infliximab (Remicade)

Remicade was 5 mg/kg IV (single dose)

Intervention Type: DRUG

Intravenous immunoglobulin (IVIG)

2nd dose of IVIG (2g/kg)

Intervention Type: BIOLOGICAL

Other Intervention Names

Gammagard, Gamunex

Eligibility Criteria

Inclusion Criteria

To be eligible for the trial, subjects must meet all of the following criteria:

1. All eligible subjects, or legal representative, must provide written informed consent/assent, prior to initiation of any study procedure.

2. Eligible subjects will be infants and children, under 18 years old, with acute KD who remain or become febrile (>/= 38.3˚ C or 101.0˚ F) after the end of the 48 h-period after completing their IVIG infusion (2gm/kg).

3. Patients must have persistent or reoccurrence of fever > 48 hours of observation to be eligible for the trial.

4. Prior to the initial IVIG treatment, patients must have been febrile for >/= 3 days and have met 4/5 standard clinical criteria (Table 1) - OR - patients with fever and 3/5 clinical criteria will be eligible if echocardiogram demonstrates at least one coronary artery segment with a Z score of > 2.

5. Patients must present for their initial diagnosis and IVIG treatment within the first 14 days after fever onset (Illness Day 14).

6. 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.

7. All eligible subjects must have a chest radiograph within one week prior to first infusion of study drug with no evidence of malignancy, infection or fibrosis.

Exclusion Criteria

If a subject has any of the following criteria, he or she may not be enrolled in the study:

1. Have been receiving corticosteroids (ie, via any route) at doses > 1 mg/kg prednisone equivalent daily.

2. Have history of TB or TB exposure.

3. Have history of histoplasmosis or coccidiomycosis.

4. Have received anakinra (Kineret®), etanercept (Enbrel®), or adalimumab (Humira®) within 1 month prior to first study drug administration.

5. Have any chronic disease, except asthma, atopic dermatitis or controlled seizure disorder.

6. Have documented history of current active hepatitis B or a history of hepatitis C infection.

7. Have documented history of human immunodeficiency virus (HIV) infection

8. Have received a transplanted organ (with the exception of a corneal transplant performed > 3 months prior to first study drug administration).

9. Have a known malignancy or history of malignancy within the 5-year period prior to first study drug administration (with the exception of squamous or basal cell carcinoma of the skin that has been completely excised without evidence of recurrence).

10. Have a history of prior lymphoproliferative disease including lymphoma.

11. Have multiple sclerosis or other central demyelinating disorder.

12. Have received any previous treatment with infliximab or other monoclonal antibodies.

13. 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.

14. Are participating in another investigative trial, involving investigational agents, during participation in this trial.

15. Have a history of substance abuse (drug or alcohol) within the previous 3 years.

16. Are pregnant, nursing, or planning pregnancy (both men and women) during the trial or within the 6-month period thereafter.

17. Have a known allergy to murine proteins or other chimeric proteins.

18. Patients with ischemic congestive heart failure.

• Maximum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Centocor, Inc.

INDUSTRY

Sponsor Role: collaborator

University of California, San Diego

OTHER

Sponsor Role: lead

Responsible Party

University of California, San Diego

Principal Investigators

Jane C Burns, M.D.

Role: PRINCIPAL_INVESTIGATOR

UCSD/CHHC

Locations

Ucsd/Chhc

San Diego, California, United States

Countries

United States

Other Identifiers

2004-0548

Identifier Type: -

Identifier Source: secondary_id

041374

Identifier Type: -

Identifier Source: org_study_id