Status and phase
Conditions
Treatments
About
The purpose of this study is to evaluate the efficacy and safety of high-dose human Immunoglobulin G Intravenous (IGIV) 10% in subjects with Kawasaki diseases (KD).
Full description
This is a multicenter, single-arm, and open-label clinical trial to evaluate the coronary artery lesions (CALs) at 2 and 7 weeks after single dose of IGIV 10% (2 g/kg) administration for at least 12 hours to evaluate the efficacy and safety of IGIV 10%.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Infants and children aged 3 months to 7 years inclusive, at the time of signing the informed consent, however, patients with complete KD are eligible up to 12 years (applies to 2A)
Subjects with fever 4-10 days meeting one of following criteria (A, B or C)
A. Subjects with at least 4 of the following principal clinical findings:
i) Bilateral bulbar conjunctival injection without exudate
ii) Erythema and cracking of lips, strawberry tongue, and/or erythema of oral and pharyngeal mucosa
iii) Erythema and edema of the hands and feet in acute phase and/or periungual desquamation in subacute phase
iv) Cervical lymphadenopathy (≥1.5 cm diameter), usually unilateral
v) Rash: maculopapular, diffuse erythroderma, or erythema multiforme-like
B. Subjects with at least 3 of the principal clinical findings and coronary artery abnormalities detected by 2-dimensional echocardiography: Z score of left anterior descending coronary artery or right coronary artery ≥2.5
C. Subjects without coronary artery abnormalities, but with fever ≥5 days, 2 or 3 of the principal clinical findings , CRP of ≥3.0 mg/dL and meeting 3 or more of the following laboratory findings:
i) Albumin <3.0 g/dL
ii) Anemia for age
iii) Elevated alanine aminotransferase level
iv) Platelet count of >450,000/mm3 after the 7th day of fever
v) White blood cell count of >15,000/mm3
vi) Urine >10 white blood cells/high-power field
Subjects whose subject's parents or legally authorized representative gave voluntary written consent to participate in the clinical trial
Exclusion criteria
Subjects with a history of KD
Subjects with following laboratory findings:
A. Platelet count <100,000/mm3
B. WBC count <3,000 cells/mm3
C. hemoglobin, hematocrit or red blood cell count more than 30% above the upper limit or 30% below the lower limit of the normal range
Subjects who are currently receiving or who have received any investigational drug or device within 30 days prior to administration of the IP
Subjects who have received TNF alpha antagonist or systemic corticosteroids within 48 hours prior to administration of the IP
Subjects who are considered by the investigator to be an unsuitable candidate for the study due to a severe chronic disease (e.g. cardiovascular disease except controllable hypertension, respiratory disease with respiratory failure, metabolic disease, renal failure, hemoglobinopathy, etc.)
Subjects who have received immunosuppressive or immunomodulatory drugs within 3 months prior to administration of the IP
Subjects with immunodeficiency including known positive serology for human immunodeficiency virus (HIV)
Subjects with a history of hypersensitivity or shock to IVIG formulations
Subjects with underlying liver disease or liver dysfunction with known etiology
Subjects with renal impairment whose creatinine level is more than twice the upper limit of the normal range
Subjects with a history of malignant tumor
Subjects with a history of IgA deficiency
Subjects who are considered by the investigator to be an unsuitable candidate for the study for any reason
Primary purpose
Allocation
Interventional model
Masking
45 participants in 1 patient group
Loading...
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal