The purpose of this study is to assess the safety and efficacy of Immune Globulin Intravenous (Human), 10% (IGIV 10%) in subjects with primary immunodeficiency disorders.

Condition	Intervention	Phase
Primary Immunodeficiency Disorders Immune Thrombocytopenic Purpura (ITP) Kawasaki syndrome	Procedure: Immune Globulin Intravenous (Human), 10%	Phase III

Further Study Details: 

Ages Eligible for Study:  24 Months and above,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

• Written informed consent obtained from either the subject or the subject’s legally acceptable representative prior to any study-related procedures and study product administration
• Diagnosis of a PID disorder as defined by World Health Organization criteria for which the subject has been receiving a regimen of IGIV infusions every 21 to 28 days over a period of at least 4 months pre-study at a dose of 300-600 mg/kg body weight
• Subjects > 24 months of age
• A negative serum pregnancy test for any female subject who is of childbearing potential.

Exclusion Criteria:

• Subjects sero-positive at enrollment for one or more of the following: hepatitis B surface antigen (HBsAg), antibodies to hepatitis C virus (HCV), antibodies to human immunodeficiency virus (HIV) Types 1 or 2
• Subjects with levels of alanine amino transferase (ALT) and aspartate amino transferase (AST) > 2.5 times the upper limit of normal for the testing laboratory. An AST > 2.5 times the upper limit of normal is allowable, if the ALT does not exceed the upper limit of the reference range for the testing laboratory
• Subjects with neutropenia (defined as an ANC >= 1,000/mm3)
• Subjects with serum creatinine levels greater than two times the upper limit of normal for age and gender
• Subjects with malignancy or a history of malignancy
• Subjects who received any blood or blood product exposure other than an IGIV and/or immune serum globulin (ISG) preparation within the 6 months prior to study entry
• Subjects with an ongoing history of hypersensitivity or persistent reactions (urticaria, breathing difficulty, severe hypotension, or anaphylaxis) following IGIV and/or ISG infusions
• Subjects with selective complete IgA deficiency
• Subjects with moderate levels of anti-IgA antibodies (>150), or subjects with lower anti-IgA antibodies who are naive to IGIV treatment. (Subjects with lower levels of IgA antibodies, whom the investigators know to have tolerated IgA containing IGIV preparations in the past, may be included if the investigator is comfortable with this)
• Subjects receiving antibiotic therapy for the treatment of infection within 30 days prior to enrollment
• Subjects who receive prophylactic antibiotics as part of their care regimen
• Subjects participating in another clinical study involving an investigational product or device within 30 days prior to study entry

California
      Children´s Hospital Los Angeles, Los Angeles,  California,  90027,  United States
Colorado
      1st Allergy and Clinical Research Center, Engelwood,  Colorado,  80112,  United States
Florida
      University of South Florida; Astha, Allergy & Immunology CRU, Tampa,  Florida,  33613,  United States
Illinois
      Rush Presbyterian - St. Lukes Medical Center, Chicago,  Illinois,  60612,  United States
Nebraska
      Allergy, Asthma & Immunology Assoc., Omaha,  Nebraska,  68124,  United States

Study ID Numbers:  160101
Last Updated:  September 10, 2005
Record first received:  September 8, 2005
ClinicalTrials.gov Identifier:  NCT00157079
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-09-13