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Safety and Efficacy Study of a 10% Intravenous Immune Globulin Solution in Subjects With Primary Immunodeficiency Disorders

Descriptive Information
Brief Title † Safety and Efficacy Study of a 10% Intravenous Immune Globulin Solution in Subjects With Primary Immunodeficiency Disorders
Official Title † A Clinical Investigation to Assess the Safety and Efficacy of Immune Globulin Intravenous (Human), 10% in Subjects With Primary Immunodeficiency Disorders
Brief Summary 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.
Detailed Description
Study Phase Phase 3
Study Type † Interventional
Study Design † Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double-Blind, Primary Purpose: Treatment
Primary Outcome Measure †
Secondary Outcome Measure †
Condition † Primary Immunodeficiency Disorders Immune Thrombocytopenic Purpura (ITP) Kawasaki Syndrome
Intervention † BiologicalImmune Globulin Intravenous (Human), 10%
Study Arms / Comparison Groups
Publications *

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information
Recruitment Status † Biological
Estimated Enrollment †
Start Date † June 2002
Completion Date December 2003
Primary Completion Date
Eligibility 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
Gender Both
Ages 24 Months - N/A
Accepts Healthy Volunteers No
Contacts ††
Location Countries † United States
Administrative Information
NCT ID † NCT00157079
Organization ID 160101
Secondary IDs ††
Responsible Party
Study Sponsor † Baxalta US Inc.
Collaborators ††
Investigators † Principal Investigator: Joseph Church, MD, Children´s Hospital Los Angeles, LA, CA
Information Provided By
Verification Date October 2006
First Received Date † September 8, 2005
Last Updated Date June 26, 2015
† Required WHO trial registration data element.
†† WHO trial registration data element that is required only if it exists.
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